Global Regulatory Affairs in Drug Development, Certificate | Part time online | University of Cincinnati | United States
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Global Regulatory Affairs in Drug Development

12 months
Duration
9576 USD/year
9396 USD/year
Unknown
Tuition fee
Unknown
Apply date
Unknown
Start date

About

The Global Regulatory Affairs in Drug Development certificate program at the University of Cincinnati is designed to provide biomedical students and professionals an opportunity to learn about the global regulatory framework within which all scientific activities and business strategies are pursued.

Overview

The development of new drugs, including biological therapeutic agents and devices is a multifaceted, complex and expensive process. It is estimated that the development of a new drug after initial stages of discovery, can take up to 15 years and cost up to $2 billion dollars. The Pharmaceutical industry in under unpresented pressure to reduce the time to market and to reduce the cost of research and development. 

Career

The graduates of this Global Regulatory Affairs in Drug Development certificate program at the University of Cincinnati are likely to find suitable jobs in the following:

  • Companies developing pharmaceutical/biopharmaceutical and devices.
  • Contract research organizations that participate in pre-clinical (ADMET) and clinical trials.
  • Contract laboratories involved in pre-clinical formulations and development of drug delivery systems.
  • Companies involved in bioanalytical and testing of drug products.
  • Contract manufacturing facilities such as those involved in pharmaceutical product manufacturing as well as specialized packaging for example the special needs for double trials. 
  • Academic Health Centers and Research Institutions and community-based research groups.

Programme Structure

Courses include:

  • Global Regulatory and Development Strategies of Drugs and Medical Devices
  • Discovery of Drugs and Therapeutic Biologicals
  • Pre-Clinical/Non-Clinical Studies for IND Approval
  • Development and Manufacturing of Drug Products and Medical Devices

Key information

Duration

  • Part-time
    • 12 months

Start dates & application deadlines

Language

English
TOEFL admission requirements TOEFL® IBT
80

Credits

12 SCH

Delivered

Online

Academic requirements

GPA admission requirements GPA
3

English requirements

TOEFL admission requirements TOEFL® IBT
80

Other requirements

General requirements

  • Students who have earned at least an undergraduate degree in chemistry, biology, engineering or related disciplines from an accredited institution are eligible to apply for admission to the certificate program.
  • Similarly, applicants with a completed professional degree such as a PharmD, MD, or DVM meet eligibility requirements.

Supplemental Application Documents:

  • Curriculum
  • Statement of Purpose

Tuition Fee

To always see correct tuition fees
  • International

    9576 USD/year
    Tuition Fee
    Based on the tuition of 4788 USD per semester during 12 months.
  • National

    9396 USD/year
    Tuition Fee
    Based on the tuition of 4698 USD per semester during 12 months.

Funding

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Our partners

Global Regulatory Affairs in Drug Development
University of Cincinnati
Global Regulatory Affairs in Drug Development
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University of Cincinnati

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