Medical Writing
The Fundamentals of Medical Writing
Being a successful medical writer requires an understanding of the drug development process, a strong grasp of scientific principles, and the ability to write clearly and effectively.
Our hands-on course for the clinical and regulatory focused individuals in the pharmaceutical industry will allow you to apply your skills to almost any regulatory document. This 12 week course will focus on learning how to interpret data and write standard regulatory documents. Also covered is a detailed background on the drug approval process and associated documentation.
Medical Writing NDA Clinical Modules
Writing the clinical documents of an standard new drug application (NDA), requires an understanding of the drug development process, a strong grasp of scientific principles, and the ability to write clearly and effectively. It also requires a grasp of the type of data included in each module as well as the key purpose each section serves.
Explore our courses
CLINICAL PROGRAMMING
These introductory courses walk the aspiring programmer through high-level concepts related to clinical programming in the life science industry.
TRIAL DISCLOSURES
In these unique courses, students will learn about the legal and ethical basis for trial disclosures and clinical trial protocols and results.
PHARMACOVIGILANCE
These courses offer entry level medical professionals the fundamentals of pharmaceutical coding and its application in clinical trial data sets.
MMS Holdings Inc.
6880 Commerce Blvd.
Canton, MI 48187, USA
Tel: (734) 245-0310
Fax: (734) 245-0320
info@mmsholdings.com
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