Intellectual property and regulatory affairs advanced certificate in San diego state university

This Certificate Programs build a foundation of knowledge focused on current laws, regulations, and good manufacturing processes mandated by major governmental regulatory agencies, specifically the Food and Drug Administration (FDA) and European Medicines Agency (EMA). Topics related to the discovery, development, testing, manufacture, commercialization, and post-marketing surveillance of pharmaceutical, biologic, and medical device products are at the core of these programs.

University online application, Official transcripts,Test scores: GRE, GMAT, TOEFL IBT-80, PBT-550, IELTS-6.5, Personal Statement, Letters of Recommendation, An undergraduate GPA of at least 3.0

Pharmaceutical, Clinical research, Quality assurance, Regulatory affairs specialist

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This Certificate Programs build a foundation of knowledge focused on current laws, regulations, and good manufacturing processes mandated by major governmental regulatory agencies, specifically the Food and Drug Administration (FDA) and European Medicines Agency (EMA). Topics related to the discovery, development, testing, manufacture, commercialization, and post-marketing surveillance of pharmaceutical, biologic, and medical device products are at the core of these programs.

University online application, Official transcripts,Test scores: GRE, GMAT, TOEFL IBT-80, PBT-550, IELTS-6.5, Personal Statement, Letters of Recommendation, An undergraduate GPA of at least 3.0

Pharmaceutical, Clinical research, Quality assurance, Regulatory affairs specialist

NA