Jun 1, 2026 · Medicines must comply with compulsory conditions referred to import and marketing authorisation, labelling and …

The task of the European Medicines Agency (EMA) is to check compliance of products distributed in parallel with the conditions laid …

Jun 25, 2025 · Authorisation is granted under the Medicinal Products (Control of Placing on the Market) Regulations 2007. The …

Jun 8, 2015 · It brings together all the existing provisions in force on the sale, production, labelling, classification, distribution and …

Since the failure of a Commission proposal on parallel imports in 1981, the EU institutions have not managed to come to any …

The EU body of pharmaceutical law and supporting guidelines that govern medicinal products and their regulatory framework.

Summary of EU directives, regulations and guidance ensuring quality, safety and efficacy of human medicines and how they are …

Information on the upcoming changes introduced by the European Union's (EU) comprehensive overhaul of its pharmaceutical …

May 31, 2026 · A structured overview of the EU regulatory framework for pharmaceutical imports, covering key legislation, GMP …

Nov 26, 2025 · Understand how parallel import of medicines works. EU/UK rules, licences, repackaging, legal risks, and sourcing tips …