We are providing services like compilation of regulatory files, DMF, Dossiers, Internal Audits, Pre-audits, Preparation for Regulatory or any other Audits, Professional training programs for skill development and Personality development for Pharmaceutical staff and technical Professionals. On site GMP and Technical Training is also our expertise and we believes in concept clearance for smooth and Quality Functioning of Pharmaceutical Industry. APC is achieved a level of Excellence in Regulatory Submissions and Compilation of Dossier, DMF For Pharmaceutical Products registration and well aware about CTD, eCTD, ACTD and other national submission requirements. We are capable of handling and answering all technical queries of registration authorities.