MEDICA PHARMING BV
MEDICA PHARMING BV
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Over Medica Pharming BV

Safeguarding Product Quality, Advancing Patient Safety & Data Integrity

  

Medica Pharming Consultancy BV is a trusted consultancy partner for pharmaceutical, biotech, and life science companies seeking excellence in Quality Assurance, Regulatory Compliance, and Technical Innovation. With over two decades of industry expertise, we guide our clients through complex GxP landscapes and help them build inspection-ready, future-proof systems that protect both patients and business continuity.

Strategic Consultancy for the Life Sciences Industry

  Medica Pharming Consultancy BV is your trusted partner in Quality, Compliance, and Innovation—delivering tailored solutions to support pharmaceutical, biotech, and life science companies worldwide. Medica Pharming is part of the Global Turnkey Projects Enterprise (GTPE) Holdings and it is primarily involved in the provision of full end-to-end drug and Process development & Quality/Compliance consultancy services .

Our Core Services

  • Quality Assurance & GxP Compliance
  • CSV & Automation Validation (MES, LIMS, OSI PI, DeltaV, PLC)
  • Regulatory Affairs & Submission Readiness
  • R&D and QC Lab Compliance 
  • Technology Transfer 
  • Biosimilar Development
  • Process Characterization and Optimalization
  • Quality by Design (QbD)

Vision

  • To be a global leader in pharmaceutical consultancy, driving innovation, compliance, and operational excellence across the life sciences industry—empowering our clients to deliver safe, effective, and high-quality therapies to patients worldwide.
  • Quality by Design (QbD)

Mission

  At Medica Pharming, we are passionate about shaping the future of pharmaceutical innovation and biopharmaceutical excellence. Our team works on high-impact projects that support drug development, regulatory compliance, process automation, and facility expansion across the globe.We’re always looking for driven, skilled professionals who are ready to make a difference in the life sciences industry. If you are ambitious, quality-focused, and eager to contribute to meaningful healthcare solutions, we’d love to hear from you.

  • Quality Assurance & GxP Compliance
  • CSV & Automation Validation (MES, LIMS, OSI PI, DeltaV, PLC)
  • Regulatory Affairs & Submission Readiness
  • R&D and QC Lab Compliance 
  • Technology Transfer 
  • Biosimilar Development
  • Process  Characterization and Optimalization
  • Quality by Design (QbD)

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