P.O. Box 42
Hexagon Tower
Blackley
Manchester, M9 8ZS
United Kingdom
We provide method development and validation services for a wide range of analytical technologies including the application of these technologies to pharmaceutical intermediates, APIs, formulations and finished products (pharmaceutical and biopharmaceutical). Our compliance with both GLP and cGMP regulations enables Intertek to support all stages of pharmaceutical development through to manufacturing. For specialist technologies validated methods can be employed to provide QC services. Methods can be developed and validated in accordance with either client-specific protocols or internal SOPs, and all methods are validated to meet MHRA, FDA and/or ICH guidelines as follows:
Method Remediation
For established pharmaceutical products, the analytical methodology that supports the production and release should undergo continuing review throughout the product’s life cycle, in terms of the validation status, efficacy and efficiency. Working within the ICH guidelines Q2 (R1) specialist pharmaceutical analysts work in conjunction with QA to provide the following services for method remediation:
Request more information to see how Intertek can help your organization with GLP & cGMP Method Development, Validation and Remediation.