Unlock the complex world of medicine and medical device regulation with “Development and Control of Medicines and Medical Devices.” This essential guide from The Bookish Owl details the rigorous tests and processes required to bring safe, high-quality products to market. Explore European registration pathways, crucial ethical considerations, and post-marketing pharmacovigilance. Understand the vital roles of regulatory bodies like the MHRA, EMEA, NICE, and international organizations such as the FDA and WHO. Ideal for healthcare students, pharmacists, and professionals in the pharmaceutical and medical device industries, this comprehensive volume provides indispensable insights into ensuring product excellence and patient safety.