FDA Regulations for Food, Drugs, Biologics, Cosmetics, and Medical Devices Including IVDs

Website https://compliance2go.com/product/?pid=CP2014-353 | Edit Freely

Category Biotechnology , Medical Device , Pharmaceutical

Deadline: September 09, 2014 | Date: September 09, 2014

Venue/Country: Houston, U.S.A

Updated: 2014-08-28 16:07:29 (GMT+9)

Call For Papers - CFP

Have you ever wondered what regulations are applicable for food, drugs, biologics, cosmetics, medical devices including IVDs in the US?

This presentation is intended to help you get familiar with the US regulations governing food, drugs, cosmetics, and medical devices and cosmetics including in vitro diagnostic medical devices (IVDs).

This presentation will present key regulatory requirements as set out in the US regulations for food, drugs, medical devices including IVDs and cosmetics. To bring medical products to the US markets, it is imperative that the firms accurately understand and interpret the relevant and applicable regulatory requirements for medical products to obtain United States (US) Food and Drug Administration (FDA)’s clearance or approval. The Federal Food, Drug, and Cosmetic Act (FD&C Act or the Act) and other statutes, if applicable, provide statutory requirements for marketing clearance or approval for food, drugs, cosmetics, and medical devices including IVDs from FDA. In this presentation, an overview of FDA regulations applicable for food, drugs, cosmetics and medical devices including IVDs will be presented.

This presentation is a must for anyone (domestic and foreign) including those who are involved in either directly or indirectly handling medical products (food, drugs, biologics, cosmetics, medical devices and IVDs).