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Pharma

9th HPAPI : Highly Potent Active Pharmaceutical Ingredients (APIs)

  • 16th – 17th September 2026
  • Italy flag Italy Milan

The 9th HPAPI Summit 2026 is the leading meeting for professionals in highly potent active pharmaceutical ingredients. With demand rising in oncology and targeted therapies, the summit spotlights the latest in process optimization, digital transformation, containment strategies, and global compliance.

Over two days of the #Ehpapi, gain insights from expert-led sessions and connect with global leaders to overcome challenges, ensure compliance, and shape the future of HPAPI development and production.

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About 9th HPAPI: Development and Manufacturing of Highly Potent Active Pharmaceutical Ingredients (HPAPIs) I #Ehpapi 2026

To be avaliable soon…

 

 

 

Who Should Attend: 

Chief Executives, Directors, Vice Presidents, Department Heads, Leaders, and Managers specialising in:    

Key Specializations

  • Manufacturing & Processing
    • Cleaning Validation
    • Aseptic Processing
    • Continuous Processing
    • Manufacturing Science & Technology
    • Process Development
    • Scale-up Operations
    • Production
  • Quality & Compliance
    • Quality Assurance/Control (QA/QC)
    • Compliance
    • Validation
    • Process Monitoring & Control
    • Internal & External Audit
    • Regulatory Affairs
    • Risk Management
  • Health & Safety
    • Industrial Hygiene
    • Occupational Toxicology
    • Corporate Toxicology
    • Health, Safety & Environment (HSE)
    • Environmental, Health & Safety (EHS)
    • Hazard Assessments
  • Research & Development
    • API and HPAPI Development
    • Research & Development (R&D)
    • Analytical Development Laboratories
    • Chemistry
    • Formulation Development
    • CMC (Chemistry, Manufacturing, and Controls)
  • Business Strategy & Commercialization
    • Business Development
    • Strategic Development
    • Commercialization
    • Licensing
    • Outsourcing

Key Specializations

  • Manufacturing & Processing
    • Cleaning Validation
    • Aseptic Processing
    • Continuous Processing
    • Manufacturing Science & Technology
    • Process Development
    • Scale-up Operations
    • Production
  • Quality & Compliance
    • Quality Assurance/Control (QA/QC)
    • Compliance
    • Validation
    • Process Monitoring & Control
    • Internal & External Audit
    • Regulatory Affairs
    • Risk Management
  • Health & Safety
    • Industrial Hygiene
    • Occupational Toxicology
    • Corporate Toxicology
    • Health, Safety & Environment (HSE)
    • Environmental, Health & Safety (EHS)
    • Hazard Assessments
  • Research & Development
    • API and HPAPI Development
    • Research & Development (R&D)
    • Analytical Development Laboratories
    • Chemistry
    • Formulation Development
    • CMC (Chemistry, Manufacturing, and Controls)
  • Business Strategy & Commercialization
    • Business Development
    • Strategic Development
    • Commercialization
    • Licensing
    • Outsourcing
REQUEST A BROCHURE

REQUEST A BROCHURE

To request an agenda for this Summit, please complete the details below. We will send you the agenda via email.

KEY PRACTICAL LEARNING POINTS

  • Advance CMC & Quality – Accelerate the development of gene and cell therapies with stronger CMC strategies and enhanced quality frameworks.

 

  • Regulatory & GMP Excellence – Stay aligned with CGTP safety, efficiency, and GMP standards to ensure compliant and reliable production.

 

  • Vector Production Scale-Up – Learn best practices to optimize, streamline, and scale vector manufacturing for higher performance and therapeutic impact.

 

  • Next-Gen Innovation – Explore cutting-edge technologies and integrated CQAs that drive efficiency, consistency, and innovation in GCT products.

 

BROCHURE

Request the 9th Annual HPAPI Summit brochure and find out the latest topics and ideas that will be shared.   

GET IT NOW

Request

Please fill in your e-mail address below, and we will process your request shortly.

Please note that some of our emails may be marked as spam due to your company’s security settings. To ensure we stay in touch, you can also connect directly with Emma at [email protected]. 

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