8
Oct
2024

ProPharma Group

Exhibitor at CPHI Milan 2024 stand 18H1, Contract Manufacturing and Services
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...

Read more Show less
Sales Markets
Show more Show less
Categories
more categories Show less
  • 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
View company profile
Contact info
Show contact info Hide contact info
Event information
CPHI Milan 2024
  • 08 Oct 2024 - 10 Oct 2024
  • Fiera Milano, Italy
  • Visit us at stand 18H1, Contract Manufacturing and Services

Products Featured at CPHI Milan 2024

  • 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. 
    ...
  • 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 ext...
  • EU/UK Qualified Person (QP) Services and MIA license

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

    Conducting clinical trials or launching products for commercialization in Europe can be a challenge. There are many complexities that can impede your efficiency to these markets, such as establishing a legal entity with a Qualified Person (QP) in the region, Brexit, and passing inspections to sec...
  • 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...
  • 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....