Advanced Materials Science Research

Regulatory Affairs Review Articles

The regulatory affairs  department of a drug company is liable for obtaining approval for brand spanking new pharmaceutical products and ensuring that approval is maintained for as long because the company wants to stay the merchandise on the market. Regulatory affairs professionals are liable for ensuring that companies within the food, drug, biotech, pharmaceuticals, medical device, cosmetics, and natural products industries follow regulatory standards for producing safe products. Regulatory affairs scientists are involved overseeing the method of getting a drug through clinical trials and onto the market. Since every step within the process of development is very regulated, those in RA work on each step to maneuver a drug from research and development through FDA approval. Many within the Regulatory Affairs Profession believe the New Approach to regulation will eventually be adopted for all healthcare products because it represents the simplest model for delivering new healthcare advances to plug during a reasonable time with acceptable safety.      

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