Devices in demand

by Admin 1. November 2008 11:17
 

The world is in the grip of an economic downturn. So how is the healthcare sector faring? In the first of a new series of articles looking at the future of medical technology, On Target performs a health check on the European medtech industry – and finds the patient is in surprisingly good health. This first article surveys the geography of the healthcare market.

At the beginning of this year, analysts predicted that the European medical device industry would grow by almost 10% in 2008. This growth, it was claimed, would be fuelled by ageing populations across Europe, increased spending on medical technologies and the accession of more fast-developing, former Eastern European states into the EU. As 2008 draws to a close, the world finds itself blighted by an economic downturn of seemingly gargantuan proportions. The double-digit growth forecast at the start of the year appears, at best, optimistic. In fact, such is the volatility of the markets at present that growth of any kind seems to be the exception rather than the rule. Despite this, the outlook for the medtech sector appears much more encouraging than that for many other global business sectors.

A recent report by management consultancy McKinsey states that the European medical technology market is growing at a rate of 5–6% each year – a model of consistency in an otherwise turbulent economic climate. Espicom Business Intelligence, a leading provider of independent market information, is even more bullish, predicting that the 11 main medical device markets in Western Europe will grow by over 40% within the next five years. Its report The Outlook for Medical Devices in Western Europe forecasts that the medical device market in these 11 key regions will reach a collective value of US$82.4 billion by 2013 – which is US$24.1 billion greater than its current position.

A recent report by management consultancy McKinsey states that the European medical technology market is growing at a rate of 5–6% each year – a model of consistency in an otherwise turbulent economic climate.

A societal challenge

The main driver for this growth is simple: demand. With or without an economic downturn, populations are ageing and patients are requiring longer and more intensive treatments. By 2025, it is predicted, the EU will have over 10 million people under the age of 20 and over 40 million retired people over the age of 60. The resultant pressures on healthcare budgets across Europe will undoubtedly be significant – but regardless, the demand for medical products will increase. Also, in the era of the ‘informed patient’, both clinicians and patients will demand access to the latest treatments. As technology advances and health outcomes improve, these societal challenges are exacerbated.

The combined impact of demand and technological advancement is creating an environment of challenge and opportunity for the medtech industry. With demand comes growth – but as healthcare deficits across Europe soar and governments battle to maintain healthcare provision in a manageable, cost-effective fashion, new healthcare policies are evolving and the medical device sector will need to operate against the backdrop of an increasingly regulated environment.

What does all this mean in practice? Where are the growth opportunities in the European market, and what challenges can companies expect along the way? John Wilkinson, former Director General of the ABHI and now Chief Executive of Eucomed – the trade association for European medtech companies – believes the industry can make a major contribution to meeting the societal challenges ahead, but that much of it will be shaped by evolving healthcare policy. “Broadly speaking, we can see a bright future for the industry,” he told On Target in an exclusive interview this month. “Demand continues to grow at a pace, largely due to demographics but also due to some new technologies that allow you to do things that couldn’t be done before. I don’t think the demand is going to go away, so there will be growth. But we are also seeing a changing policy environment: a lot more pan-European policy initiatives and subsidiarity of health to national governments. It’s clear that the Commission and parliaments are responsible for opposing strands of policy that impinge on health. A good example of that is the health technology associations, where there’s an increasingly active network of policy units around Europe, getting together to talk about shared issues.”

In addition to this, the medical technology industry in Europe currently finds itself under intense regulatory scrutiny. The effects of this will certainly influence growth. “The regulatory environment continues to evolve,” says John Wilkinson. “There’s a constant stream of either vertical regulations relating to the industry or horizontal regulations that impinge on the industry, and we need to keep our eyes on these. Specifically, the whole medical devices regulatory regime is under major strategic review by the Commission at the moment.” On Target will explore the evolution of the regulatory environment and its impact on the medical devices sector later in this series. For now, however, we take a look at the European market as a whole.

The European market

The European medical technology market is diverse and fragmented (see Figure 1). It is currently valued at €63.6 billion (2007). Germany represents the biggest market within Europe by some distance, with a 31% market share. Behind it are France (16%), Italy and the UK (both 11%) and Spain (9%), meaning that over three-quarters of the European medical devices market is concentrated into just five countries. New EU member states – Poland, the Czech Republic, Slovakia, Hungary, Slovenia, Estonia, Latvia, Lithuania, Malta, Cyprus, Romania and Bulgaria – collectively total 5% of the market, while the remaining EU 15 plus Norway and Switzerland have a combined 17% of the market – of which the Swiss market (2%) is the most mature. The medtech sector employs more than 435,000 skilled workers in Europe, comprising over 9000 companies involved in the design, manufacture and supply of medical technology. 80% of these companies are small to medium-sized enterprises (SMEs).

Germany

Germany is the third largest medical device market in the world (behind the US and Japan), with an estimated 2008 value of US$12.4 billion. Despite its size, it does not have the highest number of medtechrelated companies in Europe, sitting behind the UK in this list. According to Espicom’s 2008 report The Outlook for Medical Devices in Western Europe, domestic production of medical equipment in Germany continues to grow, but at a much slower rate than before. In 2001 domestic production grew by 12%, but by 2005 this had dropped to 3.8%. Conversely, the proportion of domestic production that has been exported has remained roughly constant: 81.9% was exported in 2001, while by 2005 this had grown to around 85%. Consequently, Germany is both the biggest exporter (€14 billion) and the biggest importer (€9.2 billion) of medical technologies. As in much of Europe, healthcare deficits in Germany are rising. In 2003, it had a healthcare deficit of €3.5 billion.

France

France is the fourth largest medical device market in the world behind the US, Japan and Germany. It is Europe’s second largest exporter of medical technology, while its imports in 2006 reached US$8.1 billion. However, not all of these imported products are destined for the domestic market. According to Espicom, the French medical device market is increasingly supplied by the foreign sales subsidiaries of multinational companies – several of which manufacture within France, having acquired smaller indigenous fi rms. Rather like Germany, France is plagued by a significant healthcare deficit – in 2003, this totaled €11.5 billion – and this has brought about a series of new health reforms under the Presidency of Nicolas Sarkozy. More specifically, recent new measures to control spending on medical devices are such that business analysts predict only moderate growth for the French market. Espicom forecasts that the sector will be valued at US$9.75 billion in 2012 (from US$7.52 billion in 2007).

Italy

Italy, alongside the UK, is the third largest medical device market in Europe by market share. Italy has over 500 medical device and in vitro diagnostics companies employing more than 30,000 people, with a combined turnover of roughly €7 billion. Around a fifth of the total turnover is generated by manufacturers with production located in Italy. Most medical device companies in Italy are SMEs (over 70%), with a combined turnover of less than €20 million. The Italian healthcare system, originally based on the UK’s NHS model, has recently benefited from a large-scale investment programme as it endeavors to thwart rising healthcare costs. In 2003 its healthcare deficit rose to €5.4 billion, from €3.2 billion twelve months earlier.

UK

The UK, like Italy, has an 11% share of the European medical device market. The UK market was valued at US$9.9 billion in 2008, and is the joint third largest domestic market in Europe behind Germany and France. In fact, the UK is home to the largest number of medical device-related companies in Europe, with 20% of European companies operating from Britain. Despite this, the UK industry is heavily reliant on imports. According to Espicom, the UK medical equipment and supplies market is undergoing an importled increase. “The value of imports (US$7.4 billion) was greater than exports (US$6.9 billion) in 2006 for the fifth time in as many years,” it says. “The UK market is proving to be a good opportunity for importers as the majority of domestic manufacturers are small and undercapitalised. This has led to inelastic domestic supply as manufacturers are unable to respond to a change in demand.”

Spain

Spain is the fifth largest medical device market in Europe and the ninth in the world. It has a strong manufacturing base, centered largely around Barcelona and Madrid, though the companies are generally small and concentrated at the low-to-medium technology end of the market. In 2006, net production was valued at US$1.5 billion, of which exports totaled US$1.1 billion. Most of the Spanish market is supplied by imports, largely from other EU 15 countries. Imports to Spain totaled US$3.2 billion in 2006, a 13.9% rise from 2005.

Central and Eastern Europe

The growth of the wider European market has, of course, been accelerated by the recent enlargement of the European Union. In 2004, eight countries from Central and Eastern Europe became full members of the EU; they were joined in 2007 by Romania and Bulgaria. The accession of these countries has not only brought in standardised regulations and opened up new markets for medical device manufacturers across the region, but has also provided them with new, attractive destinations for offshore production. According to industry analysts Frost & Sullivan, price sensitivity in the major markets is tilting the balance in favour of lower-cost products; and as prices and profit margins are squeezed, cost containment during the production phase has become very attractive. This has made the Eastern European market even more appealing. In addition to being promising markets, many Eastern European countries are also emerging as cost-effective manufacturing bases.

Russia, Poland, the Czech Republic, Hungary and the Ukraine are the five largest markets within Central and Eastern Europe. Russia has perhaps the most growth potential due to the size of its population, but its health expenditure remains low. The Czech Republic, on the other hand, has one of the highest per capita expenditures in the region, which has led to the establishment of a medical device market recently valued at US$1.2 billion. Likewise, Poland has developed an impressive market which, at US$1.8 billion in 2008, places it in the world’s top 20. Growth in Poland is expected to remain at a consistent 9% in the next few years. In Central Europe, Hungary’s medical device market currently stands at US$746 million; and with heavy investment in equipment promised, it is expected to top the US$1 billion mark within the next five years.

What the future holds

The impact of the current liquidity crisis on the medical device sector remains unpredictable. While it appears unlikely that the market will emerge unscathed by the global downturn, the European market as a whole appears well positioned for future growth. Success will, of course, depend on its collective ability to adapt to a changing regulatory environment – and crucially, its ability to provide innovative solutions to the ongoing demands of the ageing patient population. Next month, On Target will look at current therapeutic challenges and how the medtech industry is helping to overcome them.

Some of the data within this article was sourced from Eucomed (www.eucomed.org) and Espicom Business Intelligence. For further information on Espicom’s report The Outlook for Medical Devices in Western Europe, visit www.espicom.com.

 

Tags:

Medtech Features

Market Access in practice: do you have a strategy?

by Admin 1. November 2008 05:00

Everybody’s talking about market access. But far fewer appear able to define it. In the competitive world of pharmaceutical sales, developing a market access call strategy can pay dividends. But do you know what that means? WG Consulting’s Simon Dawson and Elliot Rosen report.

Throw the phrase ‘market access’ into any discussion you’re having on the challenges of promoting pharmaceuticals to the NHS, and it’s likely that the person you’re talking to will give you a knowing nod that confirms a shared, mutual intelligence. After all, it’s quite simple: if you’re not thinking about market access these days, you’re nowhere. In fact, that prolonged yet knowing silence is quite possibly disguising an inward truth: your colleague knows that market access is extremely important, but, equally, they may not completely understand what it is and how to go about doing it . In the much-vaunted ‘new NHS’, having a market access call strategy is an imperative. The questions remain: what is it and have you got one? It’s widely agreed that a rigid reliance upon the traditional approach to pharmaceutical sales and marketing is a short-cut to product failure. Why? The market isn’t changing: it’s already changed and there’s no turning back. In the past decade, the environment for the pricing and reimbursement of pharmaceuticals has become increasingly challenging. Regulation in these areas has tightened and across Europe a fourth hurdle – cost-effectiveness – has supplemented the established notions of safety, efficacy and manufacturing quality as a further requirement to secure market access. This shift has accelerated the emergence of a key group of influential stakeholders and provided the catalyst for an environment that is increasingly being controlled by payers. Achieving market access in the modern market is as much about understanding the needs of non-clinical stakeholders as it is about influencing the traditional, clinical decision-maker. But, critically, a broadbrush approach will not work. Developing an effective market access strategy requires a more customised and agile approach.

What is market access?

For the benefit of those that nod in silent agreement at the mere mention of market access, some simple definitions of the term would be helpful. There are four basic elements. Essentially, market access is about:
• considering the implications your product may have on the wider healthcare market
• understanding the impact the changing healthcare market will have on your product
• preparing a positive healthcare environment which supports uptake of your product
• communicating the ‘value’ of your product to the range of customers who influence uptake.

Strategically, market access is about packaging data in the right way, for the right customer at the right time. In a changing NHS, aligning your product with a moving target is challenging and only by understanding the needs of all stakeholders involved in the adoption, positioning and funding of your product will you be able to develop messages that improve its chances of success.

Market Access Customers

So who exactly are these new key stakeholders, and can they be defined as ‘market access customers’? Broadly speaking, these customers can be collectively termed as ‘payers’ e.g. national and local decision-makers, policy makers and budget-holders. Their emergence has challenged the industry’s stereotypical KOL mindset – historically, a typical KOL has always been a clinical KOL – but now, the rising influence of health economic, reimbursement and payer KOLs is forcing companies to redefine their sales and marketing operations. “These are very much different to pharma’s traditional clinical customer-base,” says Elliot Rosen, Management Consultant at market access specialists WG Consulting. “Whilst they are not significant in terms of their ability to prescribe a product, they will, however, be making decisions about how the services that use these products are delivered. Some may be responsible for the development or implementation of national/local guidance, and others will be directly responsible for ensuring local funding for new and existing drugs. There is no point in trying to persuade a clinician to prescribe your product if you are not able to persuade the people who hold the purse strings and have the ability to change a service or create the opportunity for your product to be used”.

Market Access Customers

• Commissioners
• Prescribing Advisors
• Head of Medicines Management
• Director of Public Health
• NICE Implementation Leads
• Chief Pharmacists
• Hospital Business Managers
• Service Managers

More disease-specific market access customers also exist, most notably in oncology. These may include:

• Cancer Network Director
• Cancer Network Pharmacist
• Tumour Site Specific Leads


“In recognition of their growing significance, pharmaceutical companies across the industry now deploy specialist market access field teams to engage directly with payers” says Elliot. “The approach, however, can vary across companies and some have adopted a more account management approach that incorporates sales and market access in one role.”

Whichever strategy is adopted, the most important thing is to ensure that the huge amount of resource being invested in the field force is being converted into valuable interactions with every customer, and every customer group. But engaging with payers in the field requires a completely different approach to more traditional industry methodology. So how do you do it? One answer is to develop a Market Access Call Strategy.

Market Access Call Strategy

Field-based market access is about being able to understand the changing NHS environment and its impact on your customer-base, and being able to adapt your contact or call strategy in response to it. “Companies need to keep on top of change, identify who the key influences are, understand their needs and respond accordingly,” says Simon Dawson, Management Consultant at WG Consulting.

“Building a call strategy is about comprehending what is ostensibly a complicated matrix. It is vital that you understand the different spheres of influence around the customers you are going to be interacting with, and, critically, the best order in which to approach those different customers to maximise those spheres of influence. Having established the best order, you also need to develop specific messages tailored to those customers, so that eventually you have a very unified understanding of your product across all the key people who are going to be making decisions as to whether to fund or use the drug you are promoting.”

“Market access is about packaging data in the right way, for the right customer at the right time”

A market access call strategy should be developed collaboratively, with sales and marketing departments working in tandem. The strategy itself will need to be dynamic enough to be able to respond to market evolution, but sufficiently planned to accommodate all known interactions. This requires an aligned approach whereby the field teams capture the challenges faced in the field and work with marketing, either to understand the materials that exist, or to develop new materials that close information gaps in the marketplace. This all needs to be drawn together into a cohesive strategy that can be understood by the field force and ultimately used to drive product uptake.

The general principle is that there is no one-size-fits-all solution. The challenges you face in your market will change according to your product, therapy area and the setting in which your treatment will be used. Only by understanding where your product fits into the wider NHS can you customise the approaches that will work best. This requires the capture, sharing and interpretation of market intelligence from the field, with garnering information being the responsibility of the market access field force.

“First of all, you need to fully understand your environment,” says Simon. “Map it. Know who your customers are and what their needs are. Talk to them, engage with them and try to build a full understanding of their sphere of influence, how they are involved with certain processes and systems and how they are going to influence prescribing. Only then should you start getting out your materials, to engage with them even more effectively.”

Market challenges

Although the various barriers to market entry will vary from product to product, a number of common general challenges exist. These challenges, which will be indicated through field-based research, will require detailed and customised responses and will drive your market access call strategy. Here are some example scenarios that commonly need addressing and will inform a market access approach:

Typical field-based market access challenges

Trying to secure funding for a drug that has a negative NICE
Trying to secure funding for a drug that is awaiting review by NICE
Ensuring the effective local implementation of NICE guidance
Ensuring the NHS has sufficient service and/or financial plans in place to support the managed entry of new drugs into the NHS
Lack of clinical demand impacting on the level of funding secured


Scenario planning is a vital aspect of market access call strategy and will play a pivotal part in determining the order in which you engage with the various customers you need to approach. “For example, in one scenario you may primarily need to interact with clinicians to achieve clinical buy-in. Following this you may need to interact with a hospital business manager to understand the impact that using your drug in a hospital will have on a Trust’s income flow. From that point, once you have got the right messages communicated to those two customer groups, you may need to go to a Cancer Network level or PCT level, with the value messages for your product almost being presented by the customers you have already engaged with. This will build a positive wave of understanding amongst your customers, and will demonstrate how understanding the various spheres of influence can work to your advantage,” says Simon.

The simple guide to a Market Access Call Strategy

1. Start by mapping and understanding the local environment – what local processes are in place? Who is involved? What is their sphere of influence? Who are the decision makers, key influencers and implementers?

2. Understand their local priorities – what are their key challenges? What are their main objectives? What information do they need/like and when?

3. Tailor your messages to the needs of the customer base – different customers will need a different approach


Despite widespread endorsement of the principles of market access in the modern market, the example above does demonstrate that whilst payers are now widely acknowledged as being highly significant and influential customers for pharma, the traditional prescriber still plays a major role in product uptake. “It is important to note the need for clinical buy-in to drive the need for market access customers to address,” says Simon.

Achieving brand success in the modern NHS requires a thorough understanding of your marketplace; the key stakeholders and influencers, their needs and objectives, knowledge of funding flows and how they work in your disease area and advanced understanding of the likely scenarios and barriers you may encounter when trying to take your product to market. To succeed, you will need a market access call strategy.

Simon Dawson and Elliot Rosen are Management Consultants at WG Consulting. WG provides a range of bespoke services to improve market access opportunities for pharmaceutical companies in the UK. For further details, please contact simond@wg-group.com

Tags:

Features

Born survivors: can redundancy be a good thing?

by Admin 1. November 2008 05:00

Redundancy has sadly become more commonplace within the pharma sales industry as the sector responds to difficult and changing market conditions. The horrors of losing your job are obvious, but is it possible to find positives and emerge stronger from the experience? Pf’s Assistant Editor Diana Spencer spoke to several redundancy survivors to find out.

However unpleasant, redundancy is now a fact of life within many industries. The current economic situation has resulted in higher redundancy figures across the labour market and research by the Chartered Institute of Personnel and Development (CIPD) and KPMG has revealed that more redundancies are on the horizon, with more than a quarter of employers planning further redundancies in the next 12 months.

Sadly, the pharmaceutical industry has not been immune to the trend. A move towards smaller sales teams and a reconfiguration of business models means that many sales professionals have recently found themselves in a consultation situation despite their hard work and good sales figures.

The fact that redundancy is so widespread today has led to a considerable shift in attitudes. It is no longer seen as an indication of poor performance, and being made redundant is very unlikely to affect your prospects of securing another job. Indeed, the circumstances could provide a timely opportunity to explore other roles or take time out for travel or further training. Pf spoke to several people who lived through the experience to find out how there really is life after redundancy.

“Things happen for a reason”

For one NHS Liaison representative, redundancy provided a legitimate reason to leave a company where she had been unhappy, as the company’s downsizing meant her entire team was no longer needed. “At the time I was very upset and angry, but it was the best thing that happened to me, as it gave me a valid reason to leave after being there for five years.”

Rather than experiencing any stigma surrounding the redundancy when applying for other jobs, she felt it actually helped to have a valid reason for leaving despite five years of success with the company. Now an occupational hazard of working in most industries, redundancy is no longer associated with an implication of professional failure.

Having successfully secured a position in another company working in a niche market, she is thankful for the chance to explore other opportunities. “I truly believe things happen for a reason and for the better. I am definitely better off now in many aspects, such as work/family balance, income and benefits, though this is an area of the industry I never would have explored had I not been made redundant.”

“My employer asked how I could leave them!”

It seems that even senior roles and those with considerable years’ service with a company are no longer immune to redundancy. One Senior RBM/Project Manager reflected on her feelings at being put into consultation despite ten years’ loyalty and being considered one of the company’s best RBMs: “It was all a bit of a blur. My whole national team were in a consultation position and I was busy managing their expectations, which was bizarre as I was about to be put into the same position.”

Having been told to look outside the company for a role, just in case there wasn’t a suitable alternative to offer, she took stock of her situation. “I was far more relaxed than I ever thought I would be. I have a family and a mortgage so I needed a salary. Fortunately, I had mortgage protection, something I would advise anyone to get. I wondered whether I should do something different or even set up my own business, and registered with a few agencies both within and outside the industry.”

An offer was made of a job she had done six years previously, but grateful to have a position at all, she accepted. However, when an agency contacted her with a position working in facial aesthetics, she realised she was ready for a change. “Now I have the most amazing national team of product specialists with my new company. My consultation process really forced me to look outside my comfort zone, something you don’t get a chance to do when you’re caught in the rat race.

“My consultation process really forced me to look outside my comfort zone, something you don’t get a chance to do when you’re caught in the rat race”

“The irony was that when I handed in my notice, the company asked why and how I could leave them! My response was to thank them for the opportunity to look outside.”

“Thank you for making me redundant!”

In the current industry climate, it is not unusual for people to experience the redundancy process more than once, and though a huge inconvenience, this should not be taken as a negative reflection on your abilities. Indeed, it is not uncommon for sales professionals to face consultation with the same company for the second time.

This was the situation of an employee of one organisation when she was informed that her contract had come to an end for the second time. “I couldn’t believe this was happening again and I was very uncertain as to the future. I ended up securing a position with the same company, but it was a step back and I was merely hanging on in the hope a management position would come up.”

When she was put forward for a job in a company outside mainstream pharmaceuticals, it seemed an ideal opportunity. “All I can say is ‘thank you for making me redundant!’ I wouldn’t have been looking for a job if I hadn’t and would never have had the opportunities that I do now.

Looking back, it was worth all the worry and uncertainty to have what I have now.”

I will survive

Redundancy is never a desirable situation. You might not have to eat live insects and build shelters in trees a la Channel 4’s ‘born survivor’ Bear Grylls, but being made redundant can leave you feeling stranded without much hope.

However, rather than being a turn downwards, with the right approach redundancy can provide real opportunities for development. Being forced to leave your company can help you get out of a rut, consider roles you never would have previously and discover where you can be happiest.

Anyone forced to cope in harsh conditions will tell you that survival is about positivity and being able to adapt to your environment. It’s important to sit back, take stock of your situation and consider where you are heading. A new direction could be exactly what you need, and it might be the threat of redundancy that provides the momentum to make that change.

Tags:

Features

Accounting for the NHS – The Annual Health Check 2007/08

by Admin 1. November 2008 05:00

The third Annual Health Check from the Healthcare Commission has now been published. Alan Jones provides a round-up of the most significant results. Have you accounted for these in your local plans?

The Healthcare Commission as an independent body has gone and is now part of the Care Quality Commission, officially live in April 2009. For its swansong, it published the latest results of the Annual Health Check for England’s 319 NHS Trusts. As companies re-invent account management for the NHS and dive deeper into customer-centric working and enhanced customer focus to achieve deep customer insight, these results provide one with a fabulously rich vein of NHS gold for local account management purposes.

What is the Annual Health Check?

Over the last 10 years or so, the NHS in England has been subject to very close scrutiny over its performance. Once upon a time we had star ratings, but these were ditched as being too narrowly focused. Then Standards for Better Health, published in 2004, went to the other end of the performance management spectrum with a vast array of 24 core standards (with 44 components) and 33 national targets. One such standard, just for interest, is the implementation of NICE technology appraisals. All NHS Trusts are asked to make self declarations as to whether they are achieving all of this (or not), the Healthcare Commission makes some spot checks and then, voila, each Trust gets a rating on a fourpoint scale ranging from excellent to weak on both quality of services and use of resources (financial management). But these are only the headline stories and so much more information is available to you.

How did the NHS do in 2007/08?

The Commission found that overall NHS Trusts had improved over previous years. In terms of quality, the Commission judged 100 NHS Trusts (26%) to be excellent, 139 (36%) good, 132 (34%) fair and 20 (5%) weak. For their use of resources, this year 94 Trusts (24%) were excellent, 145 (37%) were good, 132 (34%) were fair and 20 (5%) were weak. Overall, 42 Trusts were excellent on both measures (mostly NHS Foundation Trusts), compared with two in the first annual health check in 2005-6, while the number scoring weak on both measures has fallen from 25 to six.

One hundred and sixty-nine Acute and Specialist Trusts were the most dramatically improved, whilst PCTs’ performance disappointed overall, with only 33% rated excellent or good on quality of services, although this year Salford PCT became the first ever double-excellent PCT. Brent, Great Yarmouth & Waveney and North Yorkshire & York PCTs were all rated ‘double-weak’. And just to give you a flavour of some of the individual standards being measured: a core standard with one of the highest rates of compliance was C22b (99.3%), about requiring organisations to use annual public health reports to inform policies and practices. Knowledge of what is in these reports is also critically important for you in terms of PCT account management.

Regionally, NHS North East performed the best and NHS London the worst. In fact, London SHA was the only area of the country where performance for quality of services had declined and, for the first time, there seems to be a gap opening up with the rest of England – not surprising really since London’s small PCTs were ‘unreconfigured’ in the last re-organisation and remain weak.

Action to address these issues will likely focus on encouraging PCTs to work together to commission services and future reconfiguration of London PCTs is not out of the question. So those working the London Health Economy need to note that already a London Clinical & Business Support Agency is being formed, responsible for sharing the skills and knowledge that will enable London’s 31 PCTs to become world class commissioners – a possible new Regional Influencing Centre?

So why is all this important to me?

Well, if you are an account manager, it would make sense to know how your organisational accounts are performing and what they are being measured on. The individual Trust Annual Health Check results are vitally important to know and need to be added to any ‘sophistication indices’ you might be using. We have seen that there are 42 organisations at the top of this excellence tree (including one PCT) and six organisations at the bottom (including 3 PCTs). Now, let’s say you are calling on these organisations, surely this kind of knowledge might change the very nature of your account management strategy for a particular organisation? For instance, as far as joint working approaches to those at the top of the tree were concerned, your approach might be centred more around their innovativeness and their moving even further forward in terms of delivering improved outcomes for their patients. With those at the bottom, your approach might be more measured and possibly about helping them out of the deep black hole they are in! And a thorough analysis of the detailed results would also be needed. For instance, they might not be implementing NICE guidance and you might be able to be of some assistance here. It will be very useful for local Acute Trust, Mental Health Trust and PCT account managers to know the individual detailed results of their accounts and these can all be found on the Healthcare Commission’s website. Please see www.healthcarecommission.org.uk.

Alan Jones is an independent policy analyst and adviser. He comments widely on the implications of NHS reform and is a much sought after presenter, chair and facilitator. He can be contacted at alan.jones28@virgin.net.

Other questions are: Why have NHS Foundation Trusts done so well? What is it about this future NHS hospital model that is so different to the non- Foundation Trust? And why are PCTs doing so poorly? Also, how will this relate to PCTs moving towards becoming ‘world class commissioners’? This is particularly relevant as from this autumn, PCTs will be assessed against a whole range of new competencies. The results will eventually be made public and here too will be another rich vein of information for local account management. Finally, the Audit Commission too is an excellent source of local information, and those who want to dig more deeply into the finance side can see their recent Health Briefing Auditors Local Evaluation 2007/8 at www.audit-commission.gov.uk, where, in Appendix 2, you will find each NHS Trust’s scores in terms of financial management and value for money. For instance, Bromley PCT scores very highly here and Ashton, Leigh and Wigan PCT are mentioned in despatches for their approach to tackling health inequalities.

Deep customer intelligence has to be the way forward for account management and the ‘truth’ is indeed out there…

Tags:

Features

Cash or car?

by Admin 1. November 2008 05:00

Which company benefit drives us?

As the cost of living continues to escalate at an alarming rate, employee perks, such as a company car, can make all the difference. Interestingly, respondents to this year’s Pf Company Perception, Motivation and Satisfaction Survey voted company car policy as one of their top ten motivations, though only 45% were satisfied with this aspect of their remuneration. Paul Harrop, Sales & Marketing Director, Daimler Fleet Management, looks at how cost-cutting and environmental pressures are forcing companies to change their policies.

When changes to company car Benefit in Kind (BIK) taxation were introduced in 2002, many companies took the opportunity to review the value of the company car as an employee benefit. The reforms were fundamental, with a change from taxing engine size to taxing CO2 emissions and removing preferential treatment for those who drove high business mileage.

Employees who were financially penalised were attracted towards cash for car options to reduce their BIK tax burden. Employers also saw advantages in a salary alternative, such as potentially reduced administration from ceasing to manage a company fleet, removal of Class 1A National Insurance paid on the benefit the driver receives, and a drive to diversify their employee benefits packages.

While predictions about the decline of the company car proved to be unfounded, there have been changes and a diversification in the funding and composition of corporate fleets:
• There is a greater use of personal finance and employee car ownership schemes.
• Diesel derivative vehicles, because of their comparatively low CO2 emissions, have expanded in number within company fleets.
• Car provision is a choice within a wider and more sophisticated range of employee benefits.
• Duty of care issues are increasing the focus of attention at board level on building safety into fleet vehicle policies.

Duty of care responsibility falls to the organisation as a whole, with the directors being most at risk for legislative breaches. Although the law won’t blame individual managers for accidents, it could impose unlimited fines for a company “if the way in which any of its activities managed or organised by its senior managers causes a person’s death and amounts to a gross breach of relevant duty of care owed by the organisation to the deceased”.

An integral part of the Health & Safety at Work Act, Duty of Care requires an employer to be responsible for employee health and safety while at their place of work. Any vehicle used by an employee during the course of their work is defined as a ‘place of work’.

Assessing the options

Cash for car calculations are complex and to ensure employees taking the salary alternative are treated fairly, employers need to consider the cash allowance from the employer in lieu of company car, any BIK tax saving and the business mileage reimbursement.

Given the choice between cash or car, an employee needs to calculate cash received in lieu of a car and payments (including tax) for both scenarios, as well as the servicing, maintenance and running costs of a vehicle. A fleet management supplier will use a discounted cash flow (DCF) module to help companies to analyse whether a company car or a cash alternative is the best option.

Company involvement in assisting staff to acquire vehicles through private finance arrangements has to be handled carefully because poorly-established schemes may fail to remove BIK liability from the employee. HM Revenue & Customs (HMRC) offers the following advice to a company: “In order to review a scheme, you will need to see all the documentation which could include:
• A document or brochure outlining the scheme
• Scheme rules
• Agreements between employee and employer
• Agreements between employee and finance provider
• Agreements between employee and car provider
• Correspondence and agreements between the employer and any third parties involved, such as the finance provider and/or the car provider
• Instructions to managers about the operation of the scheme.”

By divesting itself of its car fleet, a company does not entirely drop its administrative responsibilities for work-related driving. As the HMRC guidance implies, schemes have to be rigorously structured and monitored for effects brought about by any new tax changes. This may cause particular pressures on those tasked with fleet administration when it is not their primary job function. Fleet management suppliers have the expertise to assist companies in negotiations with their local tax office, and their support can be invaluable.

Other points to consider include:
• Fuel benefit is offered by the employer is taxable as BIK based on CO2 emissions. If a pay and reclaim system is in operation, then keeping within the HMRC’s Approved Mileage Allowance Payments (AMAP) when reimbursing the employee for using a private vehicle for business purposes ensures the employee will not have a tax liability. Tax-free fuel reimbursement levels are a cause of current controversy. Unlike the Advisory Fuel Rates (AFR) for company cars, which have risen since 1 July 2008, reflecting the rise in fuel prices, the Approved Mileage Allowance Payments (AMAP) for business mileage in private vehicles have remained unchanged at 40p per mile for the first 10,000 miles and 25p per mile thereafter.
• Any cash for car scheme with employees using their own funds to acquire the vehicle means that they will incur an extra debt they wouldn’t have had with a company car. This can be an issue if they already have outstanding loans, and may bring the employer into contentious areas such as determining employee credit worthiness for the benefit of the finance provider.
• Personal finance schemes may not be suitable for companies with a high staff turnover, where leavers find themselves responsible under contract for a vehicle they may not require.
• In addition to the financial factors, it is worth considering the value of a company car from an HR perspective as a motivational HR tool. A company car, typically a prestige model, attracts high quality candidates and retains specialist and highly skilled employees. The benefit provides hassle free motoring for the employee, with servicing, maintenance, insurance, road tax and other issues being handled by the employer.

Finally, turning to operational issues, duty of care and a vehicle’s fitness for purpose are critical areas to evaluate.

Duty of care

Most companies need employees to drive for business requirements, including sales and technical support visits to customers. Employers have a duty of care for all employees driving on company business, regardless of whether they use a company car or a privately owned vehicle. Vehicles must be roadworthy, insured for business purposes and legal in every respect.

It is generally accepted that it is easier to achieve higher levels of control with company cars, particularly over the crucial area of servicing and maintenance. Failure to adequately monitor vehicles and work-related driving policies can leave companies vulnerable to prosecution under Health & Safety legislation, including the Corporate Manslaughter Act in the case of accident fatalities.

Fitness for purpose also covers many other aspects:
• Is the vehicle fit to perform the job for which it is intended?
• Does it have adequate storage and load capacity?
• Is there a requirement to carry client passengers?
• Is the vehicle suitable for the average business mileage it will cover?
• Does the vehicle fit in with the company image and environmental policy?

Duty of care issues have made many employers reconsider their policies in favour of retaining the company car. At the same time, there have been a number of developments that have changed negative perceptions about the restrictiveness of company car policies geared towards low CO2 emission vehicles:
• Manufacturers are producing an expanding range of low CO2 emission vehicles that is becoming increasingly attractive to businesses and their employees.
• Volatile fuel prices are focusing attention on fuel efficiency of greener vehicles.
• There is an increasing acceptance of the need to reduce the environmental impact of motor transport.

Daimler Fleet Management UK Limited (DFM) currently operates a UK fleet of over 58,000 vehicles, which forms part of a pan- European fleet approaching 470,000 vehicles. DFM is 8th in the Fleet News FN50 league of the UK’s contract hire providers – see www.daimlerfleetmanagement.co.uk.

For media enquiries, please contact: Ronnie Gunn, MPS & BBI International Ltd, tel.  01494 452600  01494 452600 , email ronnie.gunn@mpsuk.co.uk.

Tags: ,

Features

TextBox

Tag cloud

Calendar

<<  May 2013  >>
MoTuWeThFrSaSu
293012345
6789101112
13141516171819
20212223242526
272829303112
3456789

View posts in large calendar