We offer certified Quality Assurance, Pharmacovigilance and Regulatory services for the pharmaceutical industry. We can provide QA guidance in both the API and the FDF areas, including high potency and sterile forms. We can do audits upon request and assist you in the preparation of upcoming audits/inspections. Our objective is to assist companies to improve the level to EU-cGMP/GDP. For Marketing Authorisation Holders, we provide pharmacovigilance services for both local and global companies. Our system consists of an EU-QPPV (Qualified Person for Pharmacovigilance), Deputy EU-QPPV and a Medical Doctor. We can assist you in building the Pharmacovigilance system, including the required Pharmacovigilance System Master File and related procedures.