Because pharmaceutical development times contain, of necessity, prescribed periods which are of similar duration for competing innovator companies (eg long-term safety studies), efficiency in translating discovery research to full international development and effectiveness in optimizing the clinical and technical development programs can mean the difference between "the first and the rest," according to Trevor Jones, director, research, development and medical at the Wellcome Foundation Ltd.
He told the Financial Times/Coopers & Lybrand World Pharmaceuticals conference in London last month (Marketletters March 23 & 30) that there can be no single way of achieving this optimization. However, in the current international climate, the following "golden rules" are worth considering:
- ensuring an efficient and timely transition from discovery research to international product development;
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze