samedan logo
 
 
spacer
home > epc > autumn 2006 > outsourcing: the next generation
PUBLICATIONS
European Pharmaceutical Contractor

Outsourcing: The Next Generation

Faced with the current saturation of most developed pharma markets, Dr Michèle Piotte of Cato Research and Alexandre Prokhoroff present a remodelled value chain for the pharmaceutical company of the future

Over the last few decades, the pharmaceutical industry has been highly profitable, whilst keeping ownership of all components of its value chain. However, the traditional pharma business model is now seriously challenged by a number of market forces, such as steeply increasing drug development costs and a lack of new promising drug candidates. In response to this challenging environment, adjustments to the classic big pharma model were realised and resulted in an increased use of outsourcing and in-licensing opportunities. In this article, we would like to propose a direction for future development in order to build on lessons learnt in recent years and to provide an assessment of how current trends might influence the pharma business model.

Until recently, multinational pharmaceutical companies turned around hefty profit margins, whilst maintaining ownership of the totality of components of an all-inclusive value chain comprising three stages; drug discovery, drug development, and sales and marketing. However, the low yield of innovative therapeutic compounds, and the steep increase in drug development costs that occurred within the last decade, created the impression that a single organisation can no longer excel in each of the three categories of the value chain. This should not come as a surprise, considering that in most other industries – the airline and information technology for example – the various components of the value chain have increasingly been transferred to the responsibility of independent specialised entities, and that this latter model steadily provided noticeable value increase for the end customers.

In an attempt to counteract the effects of rising drug development costs, large pharmaceutical companies began to outsource segments of the drug development activities for which they lacked resources to contract research organisations (CROs). The rationale behind this strategy was to increase the operational flexibility, whilst aiming to reduce fixed costs and deliver a higher return on investment. This approach was based on the assumption that the development portion of the value chain was far less promising than the primary research or sales in terms of value capture. Since pharmaceutical development, and more particularly nonclinical and clinical testing, was implicitly analysed as having the potential to become a value outflow sector, it was reasoned that these activities could be outsourced without a significant negative affect on the company’s overall value creation. However, even though this business model seemed conceptually viable only a few years ago, nothing is farther from the truth in the brave new world of intense cross-sector competition for margins derived from value perception by the client.


Read full article >>

Rate this article You must be a member of the site to make a vote.  
Average rating:
0
     

There are no comments in regards to this article.

spacer
Dr Michèle Piotte received her PhD in Neuroanatomy, her MSc in Neuroendocrinology, and her BSc in Neurobiology from McGill University in Montreal, Canada. She also completed a three-year Postdoctoral Fellowship in the Department of Pharmacology & Therapeutics at McGill. Her career in the pharmaceutical industry started in 1989 when she joined the Clinical Research Department of Merck Frost Canada. Subsequently, she held scientific, managerial and business development positions at the Canadian subsidiaries of multinational pharmaceutical companies, a biotechnology company and a CRO. She has been working at Cato Research Canada in the function of Business Development Regional Director.

After approximately six years of professional experience in the business administration and financial management of pharmaceutical drug development projects, Alexandre Prokhoroff is currently pursuing an MBA at the University of Cambridge. He has received a Director’s Scholarship from the Judge Business School, as well as St Catharine’s College Benavitch Scholarship. Alexandre completed a graduate degree in Business Administration with a Dean’s Honours List distinction at Laval University (Quebec City, Canada) and has been certified by the Regulatory Affairs Professionals Society (Rockville, US). Until recently, he served as Finance and Business Development Associate at Cato Research Canada.

spacer
Dr Michèle Piotte
spacer
spacer
spacer
Alexandre Prokhoroff
spacer
spacer
Print this page
Send to a friend
Privacy statement

Industry Events

Small Scale Biomanufacturing – clinical trials, cell & gene therapies

18 September 2008, Clifton Pavilion, Bristol Zoo Gardens, Bristol

This one day conference, sponsored by bioProcessUK and organised by BioApproaches South West, will cover key, important topics relating to small scale GMP biomanufacturing.
More info >>

 
News and Press Releases

Azopharma Announces Plans to Implement XcelodoseTM Technology in the Production of Early Stage Clinical Trial Materials

HOLLYWOOD, Fla. – Azopharma Product Development Group, Inc. (“Azopharma”) announced today plans to implement Xcelodose technology at its formulations development facility, ApiCross Drug Delivery Technologies. Xcelodose technology is a powder micro-dosing system developed by Meridica. This technology offers a unique powder dispensing system for small-scale capsule filling and ultimately assists in conserving valuable research material as well as reducing various Preformulation activities.
More info >>

 

©2000-2007 Samedan Ltd.
About Us | Register | Login | Site Map | Terms and Conditions | Contact Us |
Add to favourites

Print this page

Send to a friend
Privacy statement