Faculty: Global Regulatory Affairs in Drug Development Graduate Certificate

Next Term Application Deadline

04.01.2024

Total Credits

Next Term Starts

05.06.2024

Summer 2023 Information Session

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Summer 2023 Information Session

Listen in as program director Dr. Pankaj Desai discusses the Drug Development and Pharmacogenomics programs, curriculums, work-life balance, and online school.

Learn From Nationally Renowned Faculty

The faculty staff for drug development have significant industrial experience and deep academic expertise. This unique combination of experience and expertise greatly adds to the training capabilities and strength of the program.

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Training Faculty for Drug Development

Pankaj Desai, Ph.D. Professor and Chair of Pharmaceutical Sciences Division
Richard Schwen, Ph.D., DABT, RAC Adj. Professor & Vice-President of Regulatory Affairs, Ausio Pharmaceuticals
Jianfei Jeff Guo, Ph.D. Professor of Pharmacoeconnomics
William Seibel, Ph.D., Assistant Professor, Oncology Department, Cincinnati Children’s Hospital Medical Center
Daniel Shelly, Ph.D., MBA Adj. Professor, Director of Business Development, R&D Externalization, and Clinical Development at Albumedix
Nimita Dave, Ph.D., Senior Clinical Pharmacokineticist AbbVie Inc. Adj. Assistant Professor of Pharmaceutical Sciences
Brenna Carey, Ph.D., MSDD Adj. Assistant Professor & Project Manager at Cincinnati Children’s Hospital Medical Center
Cindy Rodenberg, Ph.D., Adj. Professor, Head of Statistics for Women’s Health at P&G
Niteen Bapat, Ph.D., Adj. Professor, Senior Scientist at P&G
Ruth Stevens, Ph.D., Adj. Professor, Chief Scientific Officer/Executive VP at Camargo Pharmaceutical Services
Christopher Anderson, Ph.D., Adj. Professor, Clinical Project Manager Director at IQVIA

Learn more about the faculty of James L. Winkle College of Pharmacy

FAQs

How long does it take to complete the Global Regulatory Affairs in Drug Development Graduate Certificate?

The Global Regulatory Affairs in Drug Development Graduate Certificate is typically completed in 2 semesters or less than 1 year based on taking 2 courses per semester, which is the average pace.
What GPA do I need for the Global Regulatory Affairs in Drug Development Graduate Certificate?

For the Global Regulatory Affairs Drug Development Graduate Certificate, a grade-point average (GPA) of at least 3.00 or foreign equivalent is recommended.
What are the admission requirements for the Global Regulatory Affairs in Drug Development Graduate Certificate?
Requirements include:
- A U.S. bachelors degree from a regionally accredited college or university or an equivalent degree from a foreign country
- A grade-point average (GPA) of at least 3.00 or foreign equivalent
- Some experience in drug development or clinical research
- For international students, a Test of English as a Foreign Language (TOEFL) of at least 90 (internet-based) or 235 (computer-based), or a Duolingo English Test of at least 110 is accepted.
  - Transcripts must be submitted for evaluation to an agency recognized by the National Association of Credential Evaluating Services (NACES; www.naces.org).
Please visit the Admissions Requirements page for more information.