The Biotechnology Regulatory Affairs Graduate Certificate provides current training for professionals, who are directly or indirectly affected by biotechnology regulatory affairs. The demand for ...

In an ever-changing regulatory environment, the role of regulatory affairs personnel is essential to ensure compliance with legislation in all regions in which a company wishes to distribute its drug.

Regulatory Affairs is a relatively new field introduced by government authorities to monitor and regulate the development, manufacture, testing and marketing of drugs, medical devices, food ...

Regulatory affairs professionals may specialize in a particular geographic area (e.g., United States, European Union), in a product development phase (nonclinical, clinical, chemicals manufacturing ...

Regulatory Affairs Specialists work to ensure that biotechnology or biopharmaceutical products meet all the quality attributes — safety, efficacy, potency and purity — required by customers and ...

The Regulatory Affairs for Cell and Gene Therapy post-baccalaureate certificate program trains leaders for this growing discipline and prepares them to bring new therapeutics to market. Students learn ...

Overview Revitalize institutional workflows, elevate patient well-being, and adeptly maneuver through the intricacies of health systems. Purdue University’s online Regulatory Affairs Science for ...

“His extensive background in regulatory affairs, combined with his leadership skills, will be a tremendous asset as we continue to navigate the complex regulatory landscape and bring our sustainable ...

OIRA — the Office of Information and Regulatory Affairs — is an obscure, but powerful federal office around the corner from the White House. President Trump has decided that it should get even ...