Regulatory Landscape and Policy Developments in Implantable Pacemaker Devices: Recent Advances and Future Perspectives

Regulatory Affairs in the pharmaceutical industry play an important role as the Pharmaceutical sector is rising very rapidly. In pharmaceutical industry, it aims at the protection of human health. A Regulatory Affairs (RA) is a profession which acts as the interface between the pharmaceutical industry and drug regulatory authorities across the world. It oversees how foods, drugs, and medical products are developed, tested, manufactured, marketed and distributed to certify that they meet regulatory standards for human use. The key role of RA professional is broader than registration of products, they advise companies both strategically and technically at the highest level. Their role begins right from development of a product to making, marketing and post marketing strategies. Their advice at all stages both in terms of legal and technical requirements help companies save a lot of time and money in developing the product and marketing the same. For countries that do not have their on regulations the World Health Organization guidelines on health matters and World