Method Development

Method Development
Product Description

We are specialist in the method development of analytical methods for analysis of API, Final Drug Products or low level impurities. Usually followed by full validation in accordance to ICH guidelines.

Brightlabs

  • Country/Region:
    Netherlands
  • On CPHI since:
    2021
  • Certificates:
    2
  • Employees:
    25 - 49
Company types
Contract Service
Specifications

Brightlabs

  • Country/Region:
    Netherlands
  • On CPHI since:
    2021
  • Certificates:
    2
  • Employees:
    25 - 49
Company types
Contract Service

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  • Elemental Impurities

    Product Elemental Impurities

    Brightlabs has in-house validated methods for the analysis of elemental impurities in accordance to ICH-Q3D. Brightlabs has a unique approach for ICHQ3D, which guarantees quick turnaround times at reduced cost
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    Product Herbal Drugs Analysis

    Since 2018 Brightlabs possesses an opium exemption from the BMC (Bureau for Medicinal Cannabis), for the analysis of cannabis and related products. The combination of this opium exemption, combined with our GMP accreditation, makes Brightlabs an important partner for the analysis of cannabis and related ma...

Brightlabs resources (1)

  • Brochure NDSRI analysis

    Brightlabs has developed and validated multiple methods (GC-MS/MS & LC-MS/MS) to determine low level concentrations of Nitrosamines and NDSRIs in Drug Products