28
Oct
2025
ProPharma
Exhibitor at CPHI Frankfurt 2025 stand 6.1F85, Contract Research Organization
About Us
Categories
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NL -
2022On CPHI since
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5Certificates
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1000 - 4999Employees
Company types
Primary activities
Contact info
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ProPharma Group The Netherlands B.V., Schipholweg 73 – 75, 2316 ZL, Leiden, Netherlands
Event information
CPHI Frankfurt 2025
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28 Oct 2025 - 30 Oct 2025
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Messe, Frankfurt
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Visit us at stand 6.1F85, Contract Research Organization
Products Featured at CPHI Frankfurt 2025
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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... -
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... -
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... -
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.... -
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... -
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... -
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... -
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...
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