28
Oct
2025

ProPharma

Exhibitor at CPHI Frankfurt 2025 stand 6.1F85, Contract Research Organization
About Us

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. 

As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. 


With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmac...

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  • NL
  • 2022
    On CPHI since
  • 5
    Certificates
  • 1000 - 4999
    Employees
Company types
Consultancy
Contract Research Organisation (CRO)
Contract Service
IT/Software solution provider
Primary activities
Biopharmaceutical
Clinical Research
Contract Research Organisation
Regulatory Affairs
Supply Chain
Technology
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Contact info
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Event information
CPHI Frankfurt 2025
  • 28 Oct 2025 - 30 Oct 2025
  • Messe, Frankfurt
  • Visit us at stand 6.1F85, Contract Research Organization

Products Featured at CPHI Frankfurt 2025

  • Clinical Research Solutions

    Product Clinical Research Solutions

    We design and execute clinical trials so new therapies get to market in the quickest and safest way possible. Full-Service Solution: We manage and execute full-service clinical trials across major therapeutic areas within medical device, diagnostics, drug, and biologic. Functional Service Provisi...
  • Computer System Validation (CSV) Solutions

    Product Computer System Validation (CSV) Solutions

    ProPharma's validation professionals leverage the latest risk-based Computer System Validation (CSV) and Computer Software Assurance (CSA) techniques to ensure that our clients' systems are ready for inspections from the FDA, EMA, MHRA, and other regulatory agencies. Our consultants have extensive experien...
  • GxP Audits and Inspection Readiness

    Product GxP Audits and Inspection Readiness

    Our auditors have real world experience supporting regulatory inspections and preparing companies for pre-approval inspections. Our team of specialists includes former regulatory agency inspectors and qualified auditors who are proficient in conducting mock inspections, internal audits, vendor and s...
  • Hi-End Resource On Demand Solutions

    Product Hi-End Resource On Demand Solutions

    Project resource management includes forecasting the need to hire and/or outsource some tasks. When projects are high-value and require strategic decisions, in-house resources may be insufficient. Similarly, administrative action items are better left to contract workers so as to not overburden your staff....
  • Accelerating Your Product Through Development

    Product Accelerating Your Product Through Development

    ProPharma’s Drug Development Team is a multidisciplinary team of scientists, engineers, nonclinical, clinical, and quality experts with the experience to guide drug through development.

    Our unique combination of expertise in US and EU Regulatory Affairs, CMC, and GMP allows us to connect...
  • EU/UK Qualified Person (QP) Services and MIA license

    Product EU/UK Qualified Person (QP) Services and MIA license

    Navigating both general and country-specific regulations and requirements to supply medicinal products to the European markets can be a complex challenge for Marketing Authorization Holders (MAH). ProPharma holds both EU and UK MIA licenses which allows us to help clients overcome the complexities of su...
  • Quality & Compliance Solutions

    Product Quality & Compliance Solutions


    From early-stage development through commercial support, our experts provide critical GxP-based consulting services. We partner with clients to successfully execute projects throughout the product lifecycle to maintain quality & compliance with applicable regulations and industry standards. qq...
  • Regulatory Sciences

    Product Regulatory Sciences

    From early-stage development to post-approval, we partner with pharmaceutical, biotechnology, and medical device clients to overcome regulatory hurdles. Using science as the driver for success, we help our clients achieve positive regulatory outcomes with the Food and Drug Administration (FDA), Europea...