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Board Certification in Medical Affairs (BCMAS) Program - Extension
Board Certification - 6 Month Extension
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Accredited by IACET/ANSI
The #1 Ranked Medical Science Liaison (MSL) & Medical Affairs Training & Certification Program in the world. The BCMAS™ program is the best path you can choose to enter the MSL/Medical Affairs industry or to elevate your existing career as an MSL. Pruchase this extension and add an additional 6 months of access to your BCMAS program.
4.8 | (5k + Graduates)
$479.99
12 Modules
6 Months Access
100% Online & Self Paced
24/7 Live Chat
The following extension should only be purchased if your program access is expired or near expiration
6 Month Extension
If the access to your Board Certified Medical Affairs Specialist Program (BCMAS) has expired or is soon to be expired you will need to purchase this extension that provides an additional 6 months of access. Complete the #1 ranked medical science liaison (MSL) & medical affairs training & certification program in the world and attain your BCMAS credentials.
Frequently Bought Together
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Total Price : $2159.97
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Buy all together : $ 2159.97
Learning Objectives
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
Master These Skills
Regulatory
Compliance
Medical Devices
Diagnostics Industries
Pharmacoeconomic
Clinical Trial Design
Drug Development
REMS
Pharmacovigilance
Publication Practices
HEOR
Evidence Based Medicine
Advisory Boards
Post Marketing
Medical Information
All ACMA certifications are accredited by IACET/ANSI
25k+
Users
80+
Countries
250+
Companies
Module Breakdown
Module 1
Strategic Mastery of Medical Affairs: Core Functions, Tools & Processes
The Medical Affairs Core Functions, Tools & Processes module provides an understanding of the pharmaceutical industry's organizational structure, focusing on the strategic role of Medical Affairs in driving product development and launch readiness. Learners will explore the key responsibilities of Medical Affairs teams, the drug development pathway, and the integration of regulatory knowledge to create impactful strategies.
Module 2
Advanced Concepts in Medical Affairs: Medical Devices & Diagnostics
Explore the unique challenges and opportunities within the medical devices and diagnostics industries. This module highlights regulatory pathways, compliance, and the strategic role of Medical Affairs in shaping these sectors.
Module 3
HEOR: Strategic Insights and Modeling for Medical Affairs Professionals
This module focuses on the role of HEOR in demonstrating the value of medical products. Learn how to interpret and apply pharmacoeconomic data to support evidence-based decision-making and stakeholder engagement.
Module 4
Clinical Trial Design & Drug Development
Gain a deep understanding of clinical trial designs and the drug development process, from preclinical studies to post-marketing phases. This module emphasizes strategies to optimize trial design and align with regulatory and business goals. This module provides an in-depth understanding of how clinical trials are designed with several parameters to generate scientifically valid results. Before market approval, drugs (also medical devices or diagnostic tools) are required to go through specific phases of clinical experimentation with proven efficacy and safety. To undergo clinical trials, these phases require well-designed clinical protocols.By mastering the content in this module, medical affairs professionals will gain a deeper understanding of the complexities in bringing novel therapies to patients.
Module 5
Regulatory Affairs
The goal of this module is to provide you with an overview of the Regulatory Affairs function within a pharmaceutical company, both domestically and internationally. The module will discuss the different filings and consideration for medical devices, as well as pharmaceuticals in the United States and in the international community.
Customer Reviews
4.8 | (5k + Graduates)
Value For Money
4.8/5
Easy to Navigate
4.6/5
Program Content
4.7/5
BCMAS Credential Value
4.9/5
Reviews Mention
Perfect Resource
Competitive Edge
Attracted Recruiters
Packed with Information
Perfect Resource
Competitive Edge
Attracted Recruiters
Packed with Information
Jonathan Blaize - Associate Professor, Wagner College
The BCMAS program is a perfect resource for industry professionals, transitioning academics or anyone seeking to gain and demonstrate comprehensive knowledge of healthcare landscapes, therapeutic development and regulatory infrastructure. Scientists, particularly those with a clinical focus, will benefit immeasurably from the scope and depth offered by this course as I have. The ACMA deserves high praise for cultivating this class-leading experience!
Jaideep Banerjee, PhD, BCMAS
It's always a challenge to transition from academia to industry. And going from a medical science liaison to senior leader, you need something extra. BCMAS helped me have everything in place and helped me expand my knowledge base beyond the product knowledge. To my MSL team members, I think BCMAS can give them a competitive edge in their career.
Nneka Dimanochie, PharmD, BCMAS
I wanted to work in medical affairs as a Medical Science Liaison (MSL) in the pharmaceutical industry. With the addition of the BCMAS to my LinkedIn profile and resume, it attracted recruiters to me for medical science liaison roles. It also showed prospective hiring managers that I was a self-starter and someone who takes initiative.
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