Pharmaconsulta is an independent consultancy firm based in Malta, specializing in Pharmaceutical Regulatory Affairs. With a team of highly skilled and motivated individuals, we pride ourselves in providing the best achievable expertise across a vast range of services. These services include EU Market Access, Contract Responsible Person (RP) and Qualified Person (QP) provision, EU GMP/GDP/GACP Audits and Licensing, Falsified Medicines Directive (FMD) Decommissioning of 2D barcodes, Medical Devices, Pharmacovigilance, Laboratory Testing, Contract Manufacturing, Clinical Trials, Logistics Consultation and Warehousing, and Food Supplements and Cosmetics Registration.

In addition to consultancy services, Pharmaconsulta also offers Contract Manufacture, Laboratory Analysis, and QP Batch Release through our affiliated companies that are all GMP audited and certified. As a leading company in the field, we stay up to date with the latest industry news and articles and are committed to providing accurate and informed solutions to our clients. Contact us today to find out more about how we can assist you in navigating the complex world of pharmaceutical regulations