The Accelerated MSL Certificate was developed by subject matter experts and thought leaders from the pharmaceutical, biotechnology and medical devices industries. The program provides an in depth overview of all functional areas relevant to today’s Medical Science Liaison (MSL).
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All of the ACMA's programs are accredited by IACET/ANSI
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Covers traditional pharmaceutical, medical devices, and diagnostics industries, as well as emerging areas such as artificial intelligence (AI) and blockchain technology
Focuses on ethical and compliance issues relevant to any Medical Affairs professional
Provides a comprehensive understanding of pharmacoeconomics, clinical trial design, evidence-based medicine, drug development, REMS, and pharmacovigilance
Centers on important functional areas within Medical Affairs, such as compliant publication practices, advisory boards, continuing medical education, investigator sponsored research, and post-marketing studies
Provides basic presentation and communication skills essential for any effective Medical Affairs professional
Understand the fundamental skills you need to be an expert in clinical development. Topics include, but are not limited to: clinical trial designs, biostatistics, diagnostic tests, research & analytical strategies, data management, and evidence based medicine.
Flexible, Online, and Self-Paced Design for Busy Professionals
Pre/Post-Test Knowledge Check and Cases Studies Included To Track Your Mastery
24/7 Dedicated Live Chat Support
Learn On The Go! Mobile and Tablet Friendly Format
Pharmaceutical Industry & Drug Development
Medical Devices Overview
Diagnostics Industry
Rules governing HCP Interactions
Health Economics Outcomes Research
Evidence Based Medicine
Clinical Trial Design
Clinical Development
Presentation & Communication Skills
Regulatory Affairs
Pharmaceutical Industry Compliance
Abstract & Medical Writing
Publication Practices
Drug Development Process
Overview of Medical Information
MSLs & Field Based Medical Teams
Grants & Investigator Initiated Study Funding
Phase IV/Post Marketing Surveillance
Advisory Boards
Drug Safety
Risk Evaluation & Mitigation Strategies (REMS)