CPC carries out the detailed review of facilities, systems and documentation and carries out the gap analysis. It then creates a detailed plan in collaboration with the client and systematically guides the upgrade of the facilities to comply as per the international regulatory requirements. Additionally, it creates a formal compliance program for the client and also carries out regular audits to check for compliance to the quality management system It can effectively integrate the ISO requirements in the QMS.
CPC also imparts training in cGMP, GLP, regulatory compliances, ISO 9001:2000 etc., updating your staff’s technical competence and expand their areas of knowledge and expertise in quality management, thereby increasing their value to the company or organization.
CPC has experienced Technical Document Writers available to write quality documents. Our GMP Consultants work very closely with your technical personnel to ensure that the Quality System complies with USFDA and other international regulatory requirements. The quality documents will not only be compliant, but also quite elaborate, easy to understand and follow.