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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
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    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 & growing

    companies icon hexagon

    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
    leaders icon hexagon

    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

    Novartis

    Novartis

    Merck

    Merck

    Eisai

    Eisai

    Sanofi

    Sanofi

    AbbVie

    AbbVie

    Abbott

    Abbott

    CSL Behring

    CSL Behring

    Eli Lilly

    Eli Lilly

    Otsuka

    Otsuka

    Rutgers University

    Rutgers University

    St. John's University

    St. John's University

    Taiho Oncology

    Taiho Oncology

    Tigermed

    Tigermed

    Veeva Systems

    Veeva Systems

    Zimvie

    Zimvie

    Allergan

    Allergan

    Biogen

    Biogen

    Kura Oncology

    Kura Oncology

    Learning CC

    Learning CC

    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
    1

    AI Foundations for Medical Affairs Professionals

    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.
    2

    Strategic Mastery of Medical Affairs and AI Integration

    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.
    3

    Clinical Trial Design and Drug Development

    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.
    4

    Medical Devices, Diagnostics, and Digital Innovation

    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.
    5

    Value Demonstration with HEOR & AI

    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.
    6

    Regulatory Affairs

    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.
    7

    MSL Excellence and AI-Driven Field Insights

    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.
    8

    Drug Safety, Pharmacovigilance and Predictive Analytics

    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.
    9

    Evidence Generation and Scientific Appraisal

    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.
    10

    Business Acumen & Al Strategy in Medical Affairs

    Effective Medical Affairs leadership requires the ability to translate science into strategy. This module focuses on developing business acumen, strategic communication, and executive presence. Learners will strengthen their ability to interpret organizational priorities, demonstrate return on investment, and anticipate future trends using data-driven forecasting and analytical tools. The module also highlights how technology can support decisionmaking.
    11

    Compliance and Data Privacy in Medical Affairs

    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
    12

    Scientific Communications and Publication Strategy

    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.
    13

    Al Impact in Medical Information

    Medical Information functions as the central knowledge hub of Medical Affairs organizations. This module addresses how information teams manage scientific inquiries, develop response content, and support product lifecycle communications. Participants will explore how digital knowledge systems and Al-enabled tools can improve information accuracy, workflow efficiency, and compliance for medical information teams.

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