This premier event provides the appropriate platform to discuss and network with peers involved in pharmaceutical manufacturing, toxicology, quality control, devices, single-use systems, equipment and container development.
The summit will shed light on guideline updates, analytical testing innovations, and the impact of E&L on biologics safety.
Key Practical Learning Points of the Summit:
- Regulatory considerations and working group updates
- Single Extractable standard (BPOG, USP and ASTM)
- Standards and validation
- Innovations in analytical techniques
- E&L in quality control
- Extractables and Leachables considerations for single-use systems
- Pharmaceutical materials characterisation
- Toxicological evaluation of Leachables
- Regulatory requirements and expectations
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Use hashtag #1EL17 to connect on social media
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