Validation and Documentation

Our team of pharmacists, analytical chemists, engineers and Quality Assurance experts can help you in the preparation and/or review of a validation master plan and associated documentation. Specific validation issues like qualification of manufacturing and testing equipment, utilities, manufacturing facility, system and process validation, qualification and validation of stability testing facilities can be addressed in a cost-effective, timely and GMP compliant manner. Revalidation/Requalification due to change in process and equipment can also be taken care of.

PharmAtoZ can advise on all aspects of control, manufacturing, Quality control and Quality Assurance documentation as per WHO GMP standards. Assisstance can be provided in writing SOPs (Standard Operating Procedures), Standard Testing Procedures and various validation protocols too.