ProPharma Group

About ProPharma Group

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...

Certifications
  • CE
    CE
  • FDA
    FDA
  • GMP
    GMP
  • ISO
    ISO
  • Other
  • 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
Contact info
Meet us at

CPHI Milan 2024

Fiera Milano, Italy
08 Oct 2024 - 10 Oct 2024

Products from ProPharma Group (5)

  • 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....

ProPharma Group Resources (1)

  • News Propharma: The World's Largest RCO

    RCO Vs CRO: Drug and Device Development Outsourcing 2.0
    Traditional CRO push a full-service, "cookie-cutter" agenda, offering little compromise for the small Sponsor; ProPharma’s Research Consulting Organization RCO model leads with strategy to help de-risk programs and create tailored solutions to maximize probability of success.

    ProPharma has transformed its organizational structure and solutions to put its clients at the very center. We offer a suite of bespoke consulting solutions across service lines and functional areas of expertise to span the full product life cycle. ProPharma embraces partnerships to reduce delays and drive consistency with dedicated and experienced strategists and program managers for end-to-end oversight.