Method transfers, as a regulatory requirement, ensures a laboratory demonstrates its capability and competency to perform a method correctly. The purpose of method transfers is to avoid release of product that does not meet specification and likewise, avoid rejection of compliant product.
Whether you are looking for a new laboratory for QC release testing, or you need support on method development and validation, our team of analytical development scientists have an integrated approach for both transfers in and out of our laboratory.
When test results fall outside specification limits, it's time to investigate. Read our blog for tips on how to conduct a GMP compliant OOS/OOT investigation.
Wondering how we can help on your drug development pathway? Download our infographic to see where our services can support you from product concept to commercialisation.
Download our case study to read how we helped our client maintain regulatory compliance and extend product shelf-life through our method development, validation and stability management service.