This is the body of the EMA responsible for preparing the Agency's opinions on all questions concerning medicines for human use.
Glossary
Committee for Medicinal Products for Human Use (CHMP)
03.29.12
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Breaking News | Facilities | Industry News | Inspections
Symbiosis Completes Successful MHRA Audit
Will expand facility at its Stirling, UK site with new storage and warehousing capability.
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Drug Development | Laboratory Testing
Eliminating Endotoxins – Reagent Quality Testing for Cell and Gene Therapies
The importance of reagent quality control, especially endotoxin testing, during CGT development and the selection of reagents and suppliers to ensure safety.Garrett Perry, Technical Services Specialists at Teknova
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APIs | Drug Development
API Development Trends
Why is it important to consider solid form in API development?John Mykytiuk, Jamie Marshall and Andrew Blythe-Dickens, Sterling Pharma Solutions
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Clinical Trials | Information Technology | Reader Showcase
Almac Offers Expedited IRT Solutions for COVID-19 Trials
Launches the expedited deployment and support of multiple Interactive Response Technology (IRT) solutions in support of COVID-19 treatments
