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 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 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 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 ...