The Accelerated Medical Science Liaison (AMSL™) Certificate

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).

The Accelerated Medical Science Liaison (AMSL™) Certificate
acma is accredited

All of the ACMA's programs are accredited by IACET/ANSI

$2399.99

Earn an Accredited Certificate

Gain a Competitive Edge

100% Online

Flexible and Self-Paced

Approx. 40 Hours

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24/7 Live Chat Support

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About the Course

  • 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.

Course features include

  • 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

Topics Covered

  • 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)