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BCMAS® Program Information

Let ACMA guide you with our comprehensive, best-in-class medical affairs and medical science liaisons (MSLs) board certification program, equipping you with the expertise and skills to gain a competitive edge in the industry.

BCMAS Program Information

Accredited

Accredited by IACET/ANSI

100% online

Learn at your own pace online

40 hours

Time needed to complete

CE credits

Earn CME CE credits while learning

Credential

Earn a prestigious BCMAS credential

What is BCMAS®?

The Board Certified Medical Affairs Specialist (BCMAS®) program is the best path you can choose to enter the Medical Science Liaisons (MSL) /Medical Affairs industry or to elevate your existing career as an MSL.

This comprehensive, 12 core competencies, self-paced, e-learning, online program trains you on the core competencies crucial for success as a medical affairs or medical science liaison professional. With BCMAS certification, you demonstrate that you've mastered the industry standard of knowledge through intensive study, self-assessment, and evaluation.

BCMAS® Background

Medical Affairs and Medical Science Liaison (MSL) Professionals come from a wide variety of backgrounds. They may have backgrounds in nursing, pharmacy, medicine, or a PhD in the life and physical sciences. Medical affairs professionals work in various settings such as the pharmaceutical industry, medical device, diagnostics and biotechnology companies. They may work with medical education companies, or medical advertising agencies. Some work at Clinical Research Organizations (CROs); Site Management Organizations (SMOs); independent research and development organizations; or organizations involved in the management of clinical trials. These varying backgrounds and settings contribute to the unique knowledge and diverse expertise of the medical affairs or MSL professional.

The Accreditation Council for Medical Affairs (ACMA) has developed the first and only recognized US and International Board Certification Program for medical affairs and MSL professionals in order to create an internationally-accepted standard of knowledge, education, and experience by which medical affairs will be recognized as Board Certified Medical Affairs Specialists (BCMAS®) in the life sciences and medical communities. The standards upon which this certification program is based have been set forth by this organization to promote recognition and continuing excellence in the ethical conduct of clinical trials.

Learn more about BCMAS eligibility criteria

ACMA developed the BCMAS® Certification program to evaluate the knowledge, understanding, and application of the best practices for the profession, including the United States Code of Federal Regulations (CFR) and the ethical principles that guide good practices within medical affairs and in alignment with the principles of the Nuremberg Code, the Belmont Report and the Declaration of Helsinki. This Examination does NOT test on state, provincial, Ministry of Health, local, or institutional policy.

Meet the experts who developed BCMAS

Free Whitepaper

Becoming board certified in medical affairs : The new standard in pharma

Who should enroll in the BCMAS program?

Medical science liaisons

Medical communication specialists

Medical information specialists

Medical affairs managers

Medical affairs directors & above

Publication planning professionals

Drug safety professionals

Regulatory affairs professionals

Medical directors

HEOR liaisons

PhD professionals

Physicians

Pharmacists

Nurse practitioners

Physician assistants

BCMAS® By the Numbers

12

the number of core competencies included in the program

06

the number of months afforded to complete the program

40

the average number of hours it takes to complete the program

80+

the number of countries where our graduates reside

8000+

the number of certified BCMAS professionals worldwide

05

the number of attempts allowed for each post-quiz

04

the number of attempts allowed on the board exam

01

the number of clicks required to elevate your career

BCMAS® Program Curriculum

The BCMAS program covers life sciences understanding across pharmaceuticals, medical devices, diagnostics, and emerging areas like AI and blockchain, regulatory and compliance issues, core technical competencies in pharmacoeconomics, clinical trials, and drug development, key Medical Affairs processes such as publications and advisory boards, as well as essential soft skills for effective communication and presentations.

Life Sciences Understanding

Covers traditional pharmaceutical, medical devices, and diagnostics industries, as well as emerging areas such as artificial intelligence (AI) and blockchain technology

Regulatory & Compliance

Focuses on ethical and compliance issues relevant to any Medical Affairs professional

Core Technical Competencies

Provides a comprehensive understanding of pharmacoeconomics, clinical trial design, evidence-based medicine, drug development, REMS, and pharmacovigilance

Processes

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

Soft Skills

Provides basic presentation and communication skills essential for any effective Medical Affairs professional

BCMAS® Program Structure

Each of the 12 BCMAS core competencies includes:

Pre-Quiz (Optional)

Establishes your existing knowledge of the specific module's content

Core Competencies Content

Consists of multiple sections that vary from module to module

Post-Quiz

Determines how well you've absorbed and retained the module content

Time needed to complete

The BCMAS is a self-paced program, and you have six months of access to complete the board certification. On average, most learners complete the program within 2-3 months (approximately 40 hours). You will be given 6 months to complete the program.

Program Learning Outcomes

Align the direction and goals of a Medical Affairs organization by better understanding the cross-functional areas that relate to Medical Affairs. These areas include regulatory affairs, clinical development, marketing, compliance, and drug development

Understand health economics outcomes research (HEOR) as it relates to Medical Affairs

Learn about clinical trial design and evidence-based medicine (EBM)

Become an expert at interpreting medical literature

Broaden your knowledge in diagnostics and medical devices

Understand publication planning and regulations

Why certify with ACMA?

accredited-icon

The first and only accredited medical science liaison (MSL) and medical affairs certification program

Our certifications meet the rigorous standards of a prestigious accrediting body, reflecting our commitment to providing high quality, accredited learning opportunities.

accreditation IACET/ANSI

8000+

certified

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Trusted by professionals from top companies

The BCMAS certification has accelerated the careers of thousands of medical science liaisons and medical affairs professionals across top leading pharma companies. The ACMA works with over 250+ pharmaceutical companies

Trusted by:
GileadBaxterpfizer
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ACMA is a reputable resource in the medical affairs world for 10+ years

The ACMA is the gold standard for medical affairs education and credentialing. Our respected certification programs equip professionals with cutting edge knowledge and skills to excel across the medical affairs landscape.

4.8 /5 - BCMAS Ratings

BCMAS® is carefully constructed by industry experts

BCMAS upgrades Medical Affairs teams from “adequate” to elite

12 Core Competencies
12 Knowledge checks
Case studies
Productivity Tools
Practice exam
Final board exam
Accredited certification
AI literacy
Artificial intelligence is reshaping the way Medical Affairs professionals synthesize data, communicate scientific information, and deliver value to stakeholders. This module provides a practical foundation in AI literacy, equipping professionals with an understanding of how large language models (LLMs) function, their limitations, and how to apply them responsibly in Medical Affairs activities. Learners will gain confidence in leveraging AI tools for research, insight generation, and compliant content development while maintaining scientific integrity and data privacy.
Medical Affairs has evolved from a support function to a strategic driver of organizational value. This module establishes a foundation for understanding the structure of the pharmaceutical industry, the drug development process, and the growing role of technology in enabling Medical Affairs strategy. Participants will learn how to integrate digital innovation, AI-assisted insight generation, and cross-functional collaboration to position Medical Affairs as a core pillar of evidence- based decision-making.
Clinical trials are the foundation of evidence generation and a critical interface for Medical Affairs engagement. This module provides advanced insight into trial design, statistical considerations, and Medical Affairs contributions throughout the research lifecycle. Participants will explore the expanding use of AI in protocol optimization, patient recruitment, and data interpretation, as well as the role of Medical Affairs in supporting investigator-initiated studies and post-market research initiatives.
The convergence of devices, diagnostics, and digital health tools has transformed therapeutic innovation and patient engagement. This module equips learners with the specialized knowledge needed to navigate device classifications, combination products, and diagnostic development while understanding how digital technologies and AI are accelerating innovation. Participants will learn how Medical Affairs contributes to device strategy, regulatory alignment, and evidence generation in this rapidly evolving landscape.
In an environment defined by value-based healthcare, demonstrating product value through data-driven insights is essential. This module explores the principles of health economics and outcomes research (HEOR), including cost-effectiveness modeling, payer engagement, and real-world evidence generation. Learners will also examine how data analytics and AI-enabled modeling can strengthen value communication and inform strategic decision- making across the product lifecycle.
Regulatory Affairs serves as the bridge between scientific innovation and public health protection. This module provides global regulatory frameworks while addressing how intelligent systems and automation are influencing submission preparation, data verification, and compliance processes.
Medical Science Liaisons (MSLs) are essential for connecting science, strategy, and stakeholder engagement. This module examines the evolving competencies required for MSL excellence, including scientific expertise, relationship management, and strategic field insight collection. Participants will explore how advanced analytics, AI- assisted literature review, and insight synthesis can enhance field effectiveness and strengthen Medical Affairs’ role in evidence dissemination and decision support.
Artificial intelligence is reshaping the way Medical Affairs professionals synthesize data, communicate scientific information, and deliver value to stakeholders. This module provides a practical foundation in AI literacy, equipping professionals with an understanding of how large language models (LLMs) function, their limitations, and how to apply them responsibly in Medical Affairs activities. Learners will gain confidence in leveraging AI tools for research, insight generation, and compliant content development while maintaining scientific integrity and data privacy.
Medical Affairs professionals play a pivotal role in generating and interpreting scientific evidence to guide clinical and commercial decision-making. This module provides frameworks for evaluating study quality, synthesizing literature, and applying evidence-based medicine principles. Participants will also explore how emerging technologies can streamline literature review, automate data synthesis, and support real-world evidence strategies that enhance scientific credibility.
Artificial intelligence is reshaping the way Medical Affairs professionals synthesize data, communicate scientific information, and deliver value to stakeholders. This module provides a practical foundation in AI literacy, equipping professionals with an understanding of how large language models (LLMs) function, their limitations, and how to apply them responsibly in Medical Affairs activities. Learners will gain confidence in leveraging AI tools for research, insight generation, and compliant content development while maintaining scientific integrity and data privacy.
Ethical integrity and regulatory compliance are central to all Medical Affairs operations. This module explores global compliance standards, quality systems, and digital governance considerations as organizations adopt new technologies. Participants will learn to identify and manage data privacy risks, develop compliant workflows for AI- assisted processes, and maintain accountability through transparent documentation and review systems
Scientific communication is essential for evidence dissemination and stakeholder trust. This module examines publication planning, abstract development, and Good Publication Practice (GPP) principles while incorporating emerging methods for automation and AI-assisted writing. Learners will understand how to maintain ethical standards, ensure compliance with authorship criteria, and leverage technology to improve the efficiency and quality of scientific communication.

Free Slidedeck

The future of medical affairs and the medical science liaison role

BCMAS Program Information

Become Excellent in Medical Affairs: Become a Board Certified Medical Affairs Specialist