Two Day Best Practices for Supplier Qualification in Life Science Course: Strengthen the Quality Systems of Your Pharmaceutical, Biotechnology, and Medical Device Manufacturing ...

The evolving regulatory landscape and intensified focus on supplier qualifications present opportunities to enhance compliance and quality management. This course offers strategies for navigating ...

Non-Conformance and Corrective Action for Medical Device Manufacturers: Stay Ahead of ISO 13485, 21 CFR 820 and Other Regulations (ONLINE EVENT: June 19, 2026)

The main market opportunities lie in developing training programs and consulting services to help medical device manufacturers comply with ISO 13485 and 21 CFR 820, particularly focusing on effective ...
mccormick.northwestern.edu

CHEM_ENG 382: Biotechnology Regulatory Science

Course topics cover the intersection of science, engineering, and biotech regulatory compliance. Includes: federal regulations for drug product development, regulatory compliance processes and ...
Nature

Launching the Riyadh Roadmap for Medical Biotechnology

Under the auspices of HRH Crown Prince Mohammed bin Salman bin Abdulaziz, KAIMRC gathered global leaders in biomedical science, biotechnology and pharmaceuticals at Riyadh Global Medical Biotechnology ...