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Company Info

INTERPHEX

INTERPHEX

Academia / Non-Profit

Overview

For 41 years, INTERPHEX has been, and continues to be, the premier pharmaceutical, biotechnology, and device development and manufacturing event where you can "Experience Science through Commercialization." Sponsored by the Parenteral Drug Association (PDA), the event is based in New York and brings over 10,000 global industry professionals and 625+ industry leading suppliers together to "Learn it, Experience it, Procure it" through a unique combination of exhibits, demonstrations, partnering opportunities, networking and no cost technical conference to leverage quality, efficiency and cost effectiveness in today's ever-changing global market. INTERPHEX offers annual domestic and international industry events and educational opportunities around the world. INTERPHEX and INNOPHEX together, offer the very latest intelligence, cutting-edge technologies and state-of-the-art innovation throughout the product development life cycle.
INTERPHEX
Services and Capabilities

Services and Capabilities

Unlock Solutions, Build Partnerships, and Drive Growth at INTERPHEX 2025

April 1-3, 2025 |  Javits Center, New York, NY

Join thousands of pharmaceutical and biopharma leaders at INTERPHEX 2025—where innovation meets implementation. Whether you’re developing the next breakthrough biologic, scaling small-molecule production, optimizing supply chains, or ensuring regulatory compliance, INTERPHEX 2025 is where pharma’s trailblazers connect to solve today’s challenges and shape tomorrow’s medicines.

Claim Your FREE Exhibit Hall Pass with Promo Code: INT25PR

Register Now

Is INTERPHEX 2025 Right for You?

If you’re part of the pharmaceutical or biopharma ecosystem, INTERPHEX 2025 is where you’ll find the partners, technologies, and insights to drive your business forward.

Companies That Will Benefit:

  • Biologics, Small Molecule, Gene & Cell Therapy Innovators: Discover technologies that accelerate drug development and streamline processes.

  • Emerging Biotechs & Biosimilar Manufacturers: Build strategic partnerships with CDMOs, suppliers, and technology innovators to support growth.

  • Generics, Nutraceuticals, Compounding Pharmacies: Optimize manufacturing efficiency, ensure regulatory compliance, and discover advanced packaging solutions.

  • CDMOs & Contract Service Providers: Showcase your capabilities, connect with new clients, and explore technologies to enhance service offerings.

Key Roles That Gain Value:

  • Executive Leadership & Business Development: Identify growth opportunities, gain competitive insights, and forge new partnerships.

  • R&D, Process Development, & Analytical Leaders: Enhance process control, scalability, and leverage advanced lab technologies.

  • Manufacturing, Supply Chain, & Facility Management: Optimize workflows, improve supply chain resilience, and adopt smart manufacturing solutions.

  • QA/QC & Regulatory Professionals: Stay ahead of compliance trends, improve quality control processes, and meet evolving global standards.

Challenges You Can Solve: 

  • Accelerate time-to-market for new therapies 

  • Improve operational efficiency and reduce costs 

  • Navigate complex regulatory landscapes 

  • Enhance product quality and manufacturing scalability     

Discover innovative technologies and strategic partners INTERPHEX 2025 bridges the entire pharma ecosystem—connecting the right people with the right solutions to drive innovation, efficiency, and growth.

Claim Your FREE Exhibit Hall Pass with Promo Code: INT25PR     

Register Now

What Awaits You at INTERPHEX 2025?

  • 500+ Industry-Leading Exhibitors – Explore transformative technologies and solutions across the pharma supply chain.

  • 90+ Learning Lab Sessions – Gain insights from industry experts on the latest trends, regulations, and innovations.

  • CDMO/CMO Networking Happy Hours – Build meaningful partnerships in a relaxed setting—where deals and ideas flow seamlessly.

  • Live Sessions on the Contract Zone Stage – Learn from real-world case studies, market forecasts, and thought leadership from top contract service providers.


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Locations

  • New 60,000 ft2 state-of-the-art cGMP-compliant multi-vector production facility
  • cGMP-compliant cleanroom suites at Grade B and Grade C
  • Suspension viral vector production
  • Adherent viral vector production
  • Full suite of process development and on-site analytical capabilities
  • cGMP suites specifically designed for maximum productivity and efficient production

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