The German regulatory landscape for pharmaceutical products is governed by a complex interplay of laws and regulations. The Federal Institute for Drugs and Medical Devices (BfArM) is the primary authority responsible for ensuring the safety, quality, and efficacy of medicines within Germany. Manufacturers seeking to introduce their products in the … Read More

Importing pharmaceuticals into India requires a thorough understanding of the regulatory landscape and a meticulous adherence to established procedures. This comprehensive overview aims to demystify the process, outlining the key requirements, regulations, and documentation needed for a smooth import of medical devices into the Indian market. ,In… Read More