Whitepaper: Ten things you should know before contracting a custom synthesis project
Posted: 26 November 2018 | Eurofins | No comments yet
Companies often need to arrange for the synthesis of test substances to support research and development efforts.
There are a number of important decisions to consider before proceeding with a contract for synthesis. An adaptation of the “Five W’s” for gathering information and problem solving—Who, What, When, Where, and Why—provides a good framework for decision-making.
The rest of this content is restricted - login or subscribe free to access
Thank you for visiting our website. To access this content in full you'll need to login. It's completely free to subscribe, and in less than a minute you can continue reading. If you've already subscribed, great - just login.
Why subscribe? Join our growing community of thousands of industry professionals and gain access to:
- bi-monthly issues in print and/or digital format
- case studies, whitepapers, webinars and industry-leading content
- breaking news and features
- our extensive online archive of thousands of articles and years of past issues
- ...And it's all free!
Click here to Subscribe today Login here
Related content from this organisation
Related topics
Active Pharmaceutical Ingredient (API), Analytical techniques, Biopharmaceuticals, Bioprocessing, Bioproduction, cGMP, Clinical Trials, Contract Manufacturing, Contract Research Organisations (CROs), Formulation, Good Manufacturing Practice (GMP), Manufacturing, Material Identification, Processing, Production, Research & Development (R&D)
