Ensuring Safe Handling, GMP Compliance & Cost-Effectiveness of Highly Potent & Cytotoxic Drugs Manufacturing

From Process Safety to Rapid Scale-Up to Tech Transfer: Integrating Process Development, Industrial Hygiene & Equipment Selection to Achieve GMP Manufacturing of
Novel High Potent Drug Compounds

2023 has been a pivotal year for novel high potent compounds securing early success and approvals – from Henlius’s ADC to Gilead’s Trodelvy to BMS’s Augtyro, cementing the growth of highly potent drugs market to reach USD$40.7bn by 2023.  

The rise in novel, more potent compounds, alongside EU Annex 1, are mounting pressure on biopharma, CDMOs and equipment providers to evolve their industrial hygiene, process engineering and manufacturing capabilities to ensure safe handling and effective scale-up to achieve commercial GMP manufacturing. The 13th HPAPI: Process Development for Highly Potent Drugs Summit is your definitive community to evaluate efficient high potent compounds synthesis, adoption of innovative technology platforms and occupational safety best practice.  

Built on 12 years, this is your must-attend summit to network with 130+ like-minded individuals to 

  • Expedite safe, efficient clinical and commercial manufacturing of novel high potent drugs  
  • Explore and validation new containment solutions and technologies to optimize process development and manufacturing  
  • Increase your multi-product facility flexibility through robust design, and mitigate cross contamination with cleaning validation  
  • Effectively implement bullet-proof risk assessment of occupational exposure, and reporting system to comply with EU Annex 1  

Join 130+ experts across CMC, Process Engineering, Industrial Hygiene Leaders from Merck, Gilead, Eli Lilly in June to supercharge cost-effective, GMP compliant scale-up of cytotoxic, highly potent drugs with safety in mind! 

Join Our Process Development for High Potent Drugs
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