|
Advanced Track of the Pharmaceutical Medicine Certificate Program
The Advanced Track of the Pharmaceutical Medicine Certificate Program is
designed for physicians with more than two years of experience in the
pharmaceutical industry. The intent of the Advanced Track is to provide
experienced pharmaceutical physicians with knowledge of the evolving drug
development and regulatory process. The Advanced Track requires each physician
to select learning activities from a designated curriculum that are most
appropriate to his/her career track and goals.
The Advanced Track requires physicians to participate in five elective courses
chosen from the designated curriculum. These courses could be taken to provide
knowledge in unfamiliar subject areas needed for answering case study questions
or as refresher courses in areas where regulations and practices often are
updated. The culminating activity of the Program is the completion of the Graded
Case Study Module, which requires a response to nine case questions pertaining
to major areas of knowledge.
This Track assumes that each physician has a solid understanding of the
general drug development process and is able to identify the specific areas of
knowledge that can help him/her continue on a chosen career path or expand into
new areas.
Enroll in Program
Register for 1 core course and 5 electives from the list below.
Questions?
For questions or comments, contact us at Program
Director or (703) 276-0178.
|
Course of Study for Advanced Track
|
| |
|
Fall 2010 |
Spring 2011 |
|
Core Courses
|
Pharmaceutical Medicine Graded Case Studies
(Distance Education Course)
|
|
|
| |
|
Electives
|
Global Drug Development: Developing Plans, Protocols and Launches
|
|
|
|
|
Cancer: Pathophysiology, Current Therapies, Clinical Trials and Drug Development
|
Available
|
|
|
|
NDA Game: FDA/Industry Interaction in Drug Development
|
|
|
|
|
Essential Practices for Effective Clinical Trial Management
|
|
|
|
|
Drug Development for Pharmaceutical Physicians and Scientists - Part I
|
|
|
|
|
Adverse Events: A Review of Regulations and Challenging Exercises in Pharmacovigilance
|
|
|
|
|
Good Clinical Practices
|
|
|
|
|
Biologics Drug Development: An Integrated Overview of Manufacturing, Nonclin, Clin & Reg Requirement
|
|
|
|
|
Statistical Concepts Used in Clinical Trials
(Distance Education Course)
|
|
|
|
|
Project Management in the Research-Based Pharmaceutical Industry
|
Available
|
|
|
|
Applied Good Clinical Practices
(Distance Education Course)
|
|
|
|
|
Drug Development for Pharmaceutical Physicians and Scientists - Part II
|
Available
|
|
|
|
Regulation of Marketing and Promotion of Prescription Drugs
|
Available
|
|
|
|
Advanced Good Clinical Practices
|
Available
|
|
|