Pharmaceutical Regulatory Database of European Countries

This database provides a detailed overview of the regulation of medicines across Europe. The evaluation is conducted based on 89 parameters including various aspects of regulation such as regulatory authorities, laws on pharmaceuticals, clinical trials, good manufacturing practice (GMP), pharmacovigilance, and marketing approval systems. The database covers numerous countries with different regulatory systems such as EU-based regulation, independent national regulation, etc. In addition, where possible, database covers such information as regulatory fees in case official information is not available. Database provides a resource for professionals working in the field of regulatory affairs research, those working in drug development and students gaining knowledge on the subject.