Overview
Developing and manufacturing high-potent APIs is one of the most complex areas in pharmaceutical production. Beyond technical expertise, it requires rigorous containment, purpose-built facilities, and uncompromising safety systems to protect both operators and patients. Pharma companies must balance cross-contamination risks, process and facility design, regulatory compliance, and escalating costs, all while ensuring efficient scale-up and timely supply.
Join us for an expert led webinar on how pharma companies can manage the challenges of high potent API production, to bring advanced therapies to market faster.
What you'll learn:
- Key production challenges and proven strategies to overcome them
- Process and facility design considerations for safety and efficiency
- Managing cross-contamination risks with the right controls
- Regulatory compliance requirements and cost implications
- Scaling up from R&D to full commercialisation
- Best practices for technical transfer
- Current commercial capabilities available to support HPAPI programs
Speaker
Lidia Garcia
MSAT & New Productions Head, Recipharm
Event details
Format: LinkedIn Live webinar
Date: Thursday 11 December, 2025
Time: 15:00 - 16:00 (CET)
Duration: 1 hour
Hosted by: Recipharm
Register for our LinkedIn Live webinar