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Product Testing >> Locations >> Sweden

Eurofins BioPharma Product Testing in Sweden

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Eurofins BioPharma Product Testing Sweden AB

Rapsgatan 21
754 50
Uppsala
Sweden

Phone: +46 18 57 22 00
Fax: +46 18 57 22 22

customer.service_se@bpt.eurofinseu.com
www.eurofins.se/pharma

Equipment List


Eurofins BioPharma Product Testing Sweden

Eurofins BioPharma Product Testing Sweden AB specializes in quality assured analytical services for the biopharmaceutical industry, manufacturers of medical devices and the biotech industry. Our two laboratories, one for Chemistry and one for Microbiology, are located in Uppsala (Stockholm area).

Services:

  • Method establishment (LC, GC, Water, Spectroscopy): Development, Transfer, Validation
  • Residual solvents and Impurities testing
  • Pharmaceutical stability and release testing
  • Raw materials: Compendial and non-compendial materials
  • Stability Storage programs according to the ICH Q1A guideline
  • Non-sterile product testing
  • Sterility testing
  • Endotoxins determination
  • Facility Monitoring
  • Microbial Identification
  • Pharmaceutical Water testing
  • Facility and process validation - Environmental monitoring and Sterilization process validation
  • Cleaning & Other GMP Process Validations

Accreditations/Certifications/Registrations:

  • GMP compliant
  • FDA audited

Eurofins BioPharma Product Testing Sweden AB

Virdings Allé 2
SE 754 50
Uppsala
Sweden

Phone: +46 18 57 22 00

customer.service_se@bpt.eurofinseu.com
www.eurofins.se/pharma

Equipment List


Eurofins BioPharma Product Testing Sweden AB specializes in quality assured analytical services for the biopharmaceutical industry, manufacturers of medical devices and the biotech industry. Our two laboratories, one for Chemistry and one for Microbiology, are located in Uppsala (Stockholm area).

Services:

  • Method establishment (LC, GC, Water, Spectroscopy): Development, Transfer, Validation
  • Residual solvents and Impurities testing
  • Pharmaceutical stability and release testing
  • Raw materials: Compendial and non-compendial materials
  • Stability Storage programs according to the ICH Q1A guideline
  • Non-sterile product testing
  • Sterility testing
  • Endotoxins determination
  • Facility Monitoring
  • Microbial Identification
  • Pharmaceutical Water testing
  • Facility and process validation - Environmental monitoring and Sterilization process validation
  • Cleaning & Other GMP Process Validations

Accreditations/Certifications/Registrations:

  • GMP compliant
  • FDA audited