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European Union/Japan - The Japanese Ministry of Health, Labour and Welfare (MHLW) and the European Medicines Agency's Pharmaceuticals and Medical Devices Agency (PMDA) have started entering information on good manufacturing practice (GMP) compliance related to Japanese manufacturers into the EudraGMDP database. This is the first time that information from a non-European regulator has started to be added to EudraGMDP. The initiative is expected to speed up regulatory processes and save time for importers, manufacturers...