This is to inform that due to some circumstances beyond the organizer control, "3rd Edition of International Precision Medicine Conference" (IPMC 2023) scheduled during April 24-26, 2023 in Orlando, Florida, USA has been postponed. The updated dates and venue will be displayed shortly.
Your registration can be transferred to the next edition, if you have already confirmed your participation at the event.
For further details, please contact us at email@example.com or call + 1 (702) 988 2320.
Regulatory affairs are a field that monitors how foods, pharmaceuticals, and medical devices are produced, tested, manufactured, marketed, and distributed to ensure that they meet regulatory requirements for human consumption. At each stage of product development, regulatory affairs experts are responsible for assuring manufacturers' compliance with applicable global legislative and regulatory standards. The regulatory function in the healthcare industry is critical in ensuring the availability of safe and effective healthcare products around the world. Regulatory professionals include individuals who ensure regulatory compliance and prepare submissions, as well as those whose primary job function is clinical affairs or quality assurance. Regulatory affairs specialists play a critical part in the worldwide population's well-being by overseeing the creation and distribution of safe, healthy goods as well as medical technological breakthroughs.