Cleaning Validation

Regulatory authorities expect pharmaceutical companies to have written standard operating procedures (SOPs) detailing the cleaning processes used for various pieces of equipment. If companies have one process for cleaning between different batches of the same product but use a different process for cleaning between product changes, regulatory authorities expect the written procedures to address these different scenarios.

With advances in analytical technology, residues from the manufacturing and cleaning processes can be detected at very low levels. We are proud to provide state of art instrumentation, services and consumables to support you on your path to GMP compliance.