Programme overview
Main Subject
Pharmacy and Pharmacology
Degree
Other
Study Level
Masters
Study Mode
On Campus
The post-master's certificate in Generic Drugs studies the topics that are unique to generic drug manufacturers. Courses focus on the regulatory issues that are critical for generic industry professionals to understand if they are to ensure that their companies create safe and effective bioequivalent drugs. Coursework delves into the global business environment of generic therapeutic products and pertinent domestic and global regulations. Starting with an overview of the drug development process for innovator products, the required courses compare and explore the Abbreviated New Drug Application (ANDAs) used for generics. Elective courses enable students to explore various manufacturing and regulatory issues, including current trends in the global marketplace regarding APIs and excipients. The certificate allows students to sharpen their knowledge of this industry niche.
The Generic Drugs certificate provides the tools and information to understand how generic drugs are regulated locally, nationally and globally. Students become familiar with:
- domestic and global regulations for generic products,
- the highly competitive environment of generic products,
- manufacturing issues of global products, and
- current regulatory filing and quality assurance issues affecting generic products.
Programme overview
Main Subject
Pharmacy and Pharmacology
Degree
Other
Study Level
Masters
Study Mode
On Campus
The post-master's certificate in Generic Drugs studies the topics that are unique to generic drug manufacturers. Courses focus on the regulatory issues that are critical for generic industry professionals to understand if they are to ensure that their companies create safe and effective bioequivalent drugs. Coursework delves into the global business environment of generic therapeutic products and pertinent domestic and global regulations. Starting with an overview of the drug development process for innovator products, the required courses compare and explore the Abbreviated New Drug Application (ANDAs) used for generics. Elective courses enable students to explore various manufacturing and regulatory issues, including current trends in the global marketplace regarding APIs and excipients. The certificate allows students to sharpen their knowledge of this industry niche.
The Generic Drugs certificate provides the tools and information to understand how generic drugs are regulated locally, nationally and globally. Students become familiar with:
- domestic and global regulations for generic products,
- the highly competitive environment of generic products,
- manufacturing issues of global products, and
- current regulatory filing and quality assurance issues affecting generic products.
Admission Requirements
Scholarships
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