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    China Business
     Nov 18, 2011


Pharma adds China booster
By Benjamin A Shobert

Few sectors are more sophisticated in their view of the Chinese economy than the Western pharmaceutical industry. Much of this sophistication is a by-product of their realization very early into China's opening that it would be a long time, if ever, before the industry could realize any cost advantages as a result of exporting products from China and that, because product quality is such an important factor for pharmaceutical materials, consumers would be unlikely to trust Chinese-made medicines any time soon.

As a consequence, American and European pharmaceutical companies quickly came to terms with China as a potential market, where most other firms saw China initially as a source of low-cost production. Overall, multi-national pharmaceuticals have been very early into the process of learning how to sell and

 
market in the domestic Chinese market.

Pharma's success in these areas is no small feat. According to IMS Health, China is on track to become the world's third largest pharmaceutical market by 2013.

In the first quarter of 2011, JPMorgan estimated that pharmaceutical sales amounted to over US$5.3 billion for the top 10 American and European pharma multinationals alone. Pfizer's domestic China sales are now approaching $1 billion a quarter, while Johnson & Johnson, a latecomer to the domestic Chinese market, has sales approaching $300 million a quarter.

For most of the multinational companies in the JPMorgan report, the Chinese market is growing around 30% year-over-year. Given the uncertainty surrounding healthcare reform in the American market in particular, China remains one of the bright spots for the pharmaceutical sector.

The greatest challenge facing pharmaceutical companies operating in China - both multinationals and domestically owned firms - are changes to China's healthcare payment process. With a rapidly aging population, the healthcare sector in China is likely to be one of the most volatile growth markets for companies; however, much remains unknown.

First, the government is still defining what it will pay for (which services for particular disease states). Second, once China defines what it will pay for a particular service, it puts very strict controls in place over how much it will pay.

This has presented some unique challenges to pharmaceutical companies in China, two of which were just fined by the central government this week over allegations of price fixing on precursor materials needed for common blood pressure medications.

In 2009, Beijing put forward the government's Essential Drug List (EDL), which the October JP Morgan report stated would mean that "over three hundred Western and Chinese medicines are expected to be sold at government-controlled prices". Analysts at outside firms like JPMorgan and Citi have pointed out that this presents a potential problem that could greatly reduce profit margins for both domestic and multi-national pharmaceutical firms operating in China.

As the JPMorgan report emphasized, "With a reduction in price for pharmaceutical companies whose products fall under the EDL, profit margins will shrink while the exclusive rights to produce these drugs should theoretically boost sales volumes." Some companies have suggested that even if they win Chinese government contracts with lucrative volumes, their profit margins are so poor that they will be unable to invest in developing new drugs.

Currently, price pressures have hit domestic Chinese pharmaceuticals the hardest. At the same time as these companies struggle to meet Beijing's demands on the pricing front, they are wrestling with the changing expectations from their government in terms of the compliance standards to which they will be held.

Stephen Sheng, the Asia Pacific Region Representative for Double Dragon Consulting, a consulting firm that provides engineering, quality/regulatory, and aseptic operations services for life sciences companies that must meet US and European Union drug regulatory requirements, notes that "With the roll out of the 2010 GMPs [good manufacturing practices] by the Chinese government, the sFDA [China's equivalent of the US Food and Drug Administration] is sending a loud and clear message to the pharmas in China that time is running out and globalization is imminent."

China's domestic producers have certain advantages over their multi-national peers: government sponsorship and home field advantage are just two. However, they also face extremely sophisticated competition from established American and European pharmaceutical companies that know how to play the complicated game of managing government regulations in such a way as to maximize the profitability of their businesses. Climbing the sFDA's hill is a challenge to China's domestic producers but reflects an existing competency by their foreign competitors.

Like many industries, the pharmaceutical sector is closely watching Beijing's policy stance as healthcare reform presents both an incredible opportunity to expand coverage to China's 1.3 billion under-served consumers, but also a challenging market where rigid price controls and unclear government payment practices remain significant challenges.

Both domestic Chinese and multinationals anticipate coverage will broaden and reimbursement rates will grow, but multinationals in particular are keeping a close eye on whether Beijing begins to ask them to transfer technology to domestic partners as a trade for market access.

Given the public policy implications to making sure pharmaceutical products remain accessible to China's population, these companies also face many of the same challenges other high-tech firms in information technology and clean-tech in particular are struggling with. Where the government believes its interests do not align with those of private industry, it will likely move to protect its own interests before considering what such adjustments signal to market players. But in an increasingly saturated and mature Western healthcare market, multinationals know they have to find a strategy for success in China.

For many Western pharmaceutical companies, while they may not be able to export production of drugs from America to China, what they have found can be exported is the research and development of new drugs from America to China. Faming Zhang is the chief executive officer of Waterstone Pharmaceuticals, a company that specializes in the outsourcing of clinical research and drug discovery from the United States to China. He says that the decision to move research to China is driven by "relatively cheaper talent pool and broad patient access".

In many ways, what Western pharmaceutical companies are finding as they work with Chinese companies like Waterstone is that they can push forward with drug discovery more cost effectively than they could in the West. This represents an important challenge to advocates of globalization. Historically, the strongest advocates for globalization have argued that the path forward for developed economies is to move up the value chain into increasingly higher technology work.

To watch as modern pharmaceuticals find they can access cost effective and highly motivated workers in China is a challenge - as Howard Marks of Oaktree Capital asked in remarks at last week's Asian Venture Capital Journal meeting in Hong Kong, "where do the jobs come from in the West?"

While the answer to Marks' question today may not be clear, what is coming into focus is that China's strategy of moving up the value chain into higher technology sectors like pharma is reaping early benefits that both benefit multinationals and further refine the model for how the American and Chinese economies can work together in the 21st century.

As can be imagined, the sort of relationship companies like Waterstone have with their multinational customers is not absent risks for both parties. Multinationals in particular realize that their intellectual property (IP) risk must be properly managed under such an arrangement, but Zhang believes that "the higher IP risk in China is more of a perception".

Zhang advocates that Western companies have "strict contracts with Chinese partner, and always have active patent protection. Like many of Waterstone's competitors, these new Chinese-based drug-discovery firms that serve large multinational pharmaceutical companies are usually founded, capitalized and managed by Chinese-born, Western-educated managers who worked at a Western pharmaceutical company before starting their business.

Along these lines, some US-based pharmaceutical start-ups are also evaluating China with an eye towards lower cost drug discovery, clinical trials and, in some rare cases, capital for their company. According to Zhang, many of these early-stage pharmas have a "China connection", but he cautioned that Chinese capital can bring with it some challenges. Specifically, "the demonstration of profitability within less than five years, because Chinese investors look at short-term return more importantly [than long-term]."

Few industries encompass the challenges and opportunities within the Chinese market as broadly as pharma. The needs for basic drugs to treat diabetes, heart disease, vaccines and other conditions that Americans take for granted as highly treatable conditions remain significant problems in China. This is the great opportunity that drives multinationals as they expand within the country.

Yet, China's market is heavily reliant on government sponsorship. In China, such sponsorship traditionally comes with heavy obligations felt at a minimum through price controls and, in many of the extreme cases where Beijing's domestic policy considerations take a front seat, in the form of government forcing technology transfer.

Benjamin A Shobert is the managing director of Teleos Inc (www.teleos-inc.com), a consulting firm dedicated to helping Asian businesses bring innovative technologies into the North American market.

(Copyright 2011 Asia Times Online (Holdings) Ltd. All rights reserved. Please contact us about sales, syndication and republishing.)


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