Integrated Pharmacovigilance
Special Topics – Medical Coding
This 4-week course will focus on learning about the fundamental pharmaceutical coding dictionaries, MedDRA and WHOdrug, and how they are used on clinical trial safety data sets.
This program is designed for the entry level medical professional, M.D., P.A., master’s level medical and allied medical professional interested in exploring medical coding opportunities within the pharmaceutical industry.
Integrated Pharmacovigilance
This 10 week course will also focus on concepts like aggregate reports, signal detection, and the risk management process. Additionally, this course has a special module on medical coding, including MedDRA dictionary and WHO Drug dictionary coding.
This course is aimed to provide fundamental knowledge of how drug safety is monitored, how adverse events are reported, and a background of the safety system software used in these processes.
CLINICAL PROGRAMMING
These introductory courses walk the aspiring programmer through high-level concepts related to clinical programming in the life science industry.
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TRIAL DISCLOSURES
In these unique courses, students will learn about the legal and ethical basis for trail disclosure and clinical trial protocols and results.
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MEDICAL WRITING
These courses are for the clinical and regulatory focused individuals in the pharmaceutical industry and allow you to apply your skills to almost any regulatory document.
