This program provides a comprehensive and balanced education focusing on the key areas of Regulatory Affairs. Provided as an introduction to the field, this program was developed from increasing demand in the local biotech community. To completely master the field of Regulatory Affairs, a Professional Certificate is recommended. The certificate program is comprised of four courses: two are required and two are selected from the list of electives.
|Course Title||Course Number||Units||FA||WI||SP||SU|
|Regulatory Requirements for Drugs & Biologics||O||O|
|Regulatory Compliance for Drugs & Biologics||O||O||O||O|
|Electives (5 units are required.)|
|Electronic Submissions in Life Sciences - Planning for Success||O|
|Good Clinical Practices||O||O||O||O|
|Good Laboratory Practices||O||O||O|
|Good Manufacturing Practices||O||O|
|Overview of International Regulatory Affairs||O|
|Overview of Regulatory Affairs for Medical Device Professionals||O||O|
|L=La Jolla M=Mission Valley O=Online U=University City X=Location TBA|
Certificate registration is required to complete the program. Candidates are encouraged to register in the certificate program as early as possible to take advantage of program benefits. See Certificate FAQs for more information.
|Certificate Section ID:||100620||Add to Cart|
|Contact:||Life Sciences, (858) 534-9353|