What Are the Duties of the Consumer Healthcare Regulatory Affairs?

Professionals in regulatory affairs work for industry, academia and government entities to provide safe and effective consumer health care products to the public. Regulatory affairs professionals involved in consumer health care regulate compliance concerning a variety of products, including pharmaceuticals, cosmetics, medical devices, veterinary products and biotechnology.

Regulation Procedure

• Health care regulatory affairs employees go by government and industry standards to analyze and identify compliance product issues. The employees provide appropriate actions based on regulations so organizations can make the best decisions to meet compliance guidelines. Regulatory employees also prepare submissions and quality assurance regarding products.

Clinical and Nonclinical Studies

• Regulatory professionals make clinical and nonclinical studies concerning health care products. The employees ensure the safety of those who choose to participate in clinical tests and use regulated products. Regulatory affairs professionals have a duty to clinical study participants to make sure the benefits outweigh the risks concerning health care products.

Product Information

• Consumer health care regulatory affairs employees have the duty to provide important product information regarding the product's safety and effectiveness to physicians and other health care providers. The employees provide up-to-date, accurate reporting, giving an unbiased dissemination of information for the welfare of the public while still keeping the long-term interests of government and industry product makers.