Pharmaceutical Impurity Testing

Pharmaceutical Impurity Testing
Product Description

Our GMP compliant laboratories provide pharmaceutical impurity testing for new drug substances (ICH Q3A(R2)) and new drug products (ICH Q3B(R2)) which can support your product development from an early stage and across the lifecycle of your drug product including method development / validation and difficult matrices, offering highly sensitive and specific method development and validation expertise for residual solvents, process impurities, extractables & leachables, elemental impurities (ICH Q3D) and genotoxic impurities such as N-nitrosamines. 

To learn more, visit our website:

www.intertek.com/pharmaceutical/gmp-cmc-laboratory/pharmaceutical-impurity-testing

Intertek Analytical Services

  • GB
  • 2015
    On CPHI since
  • 4
    Certificates
  • 1000 - 4999
    Employees
Company types
CMO/CDMO
Consultancy
Contract Research Organisation (CRO)
Contract Service
Drug delivery device Supplier/Manufacturer
Manufacturer/Innovator
Primary activities
Analytical Services
Contract Research Organisation
Laboratory Services
Medical Devices
Packaging & drug delivery
Supply Chain
Specifications
  • Supplied from
    Switzerland; United Kingdom; United States

Intertek Analytical Services

  • GB
  • 2015
    On CPHI since
  • 4
    Certificates
  • 1000 - 4999
    Employees
Company types
CMO/CDMO
Consultancy
Contract Research Organisation (CRO)
Contract Service
Drug delivery device Supplier/Manufacturer
Manufacturer/Innovator
Primary activities
Analytical Services
Contract Research Organisation
Laboratory Services
Medical Devices
Packaging & drug delivery
Supply Chain

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    Visit www.intertek.com/pharmaceutical for more information.