Understanding eTMF September 03, 2015, 1:00 - 4:45 PM CEST, Online conference
As life sciences companies move to semi-virtual environments, keeping only the most vital functions in house, more and more Trial Master Files are being converted to an eTMF format...
Orphan Drugs Patient Access September 23, 2015, 2:00 - 5:15 PM CEST, Online conference
The market for orphan drugs represents a major growth area for pharma and biotech companies. Find out more about the need for collaboration between policy makers, patient organizations, researchers and businesses...
BRIC Biosimilars Approval Pathways September 30, 2015, 2:00 - 4:30 PM CEST, Online conference
Are you familiar with the most recent regulatory initiatives on the biosimilars market in BRIC countries? Our speakers’ valuable contributions will provide you with the answers...
- Cold Chain. GDP Guidelines, Audits and Regulations
- Interactive Response Technologies: Best practices and innovations
- Workforce Analytics
- Pharma Serialization: FMD Strategies
- Regulatory Affairs in ASEAN: Timelines and Strategies
- eSubmission Updates 2015
- The Business Case of Diversity & Inclusion
- Leadership Development
- Generics: EU Regulatory Landscape
- Social Media and Data Mining in Pharmacovigilance