Biopharmaceutical quality control

🔬 Your products are unique, and their quality control must be secured. We operate from clinical batches to commercial batches to ensure the safety, compliance, and quality of your products.

At CEBIPHAR, we combine responsiveness, reliable results, and scientific expertise to support your projects from Drug Substance (DS) to Drug Product (DP), including raw materials, packaging and process development.

👉 An end-to-end continuum : from molecule to market

The range of our services :

Drug Substance : analysis, stability, impurities
Drug Product : excipients, formulation, packaging integrity, stability
Process & Raw Materials : quality control, residue testing

 

 

 

Expertise

Proposed test families

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Business process

Discover the 4 phases of the life cycle of the analytical method

Interactions process

Our differentiating strengths

1

Scientific expertise :

  • Lipid formulations (mRNA vaccines)
  • Process-related impurities (transfection agents, antibiotics, …)
2

State of the art equipment :

  • Next-generation CAD detector dedicated to lipid quantification (mRNA vaccines)
  • Capillary electrophoresis, SDS-PAGE, ELISA, LC-MS/MS
3

Controlled storage capacities :

  • -80 °C, -20 °C, +5 °C to ensure sample integrity and stability
4

R&D commitment :

  • Continuous investments and new expertise to address your challenges

CEBIPHAR teams make every effort to meet the essential needs in a Quality Control partnership: communication and on time delivery

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The main objective of our Newsletter is to focus on one of our services by showing the added value it can bring you.

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