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The Medical Affairs Competency Certificate (MACC) Program
Certification Program
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Accredited by IACET/ANSI
Medical Affairs/MSL job ready skills that get you ahead in the pharmaceutical industry. Learn about drug development phases, clinical research best practices, pharmaceutical industry, compliance 101, medical science liaisons best practices, engaging key opinion leaders (KOLs), regulatory affairs, and lifecycle management.
4.7 | (500 + Graduates)
$1799.99
7 Modules
6 Months Access
100% Online & Self Paced
Earn CME/CE Credits
Frequently Bought Together
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Total Price : $4918.98
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Buy all together : $ 4918.98
Learning Objectives
Life Sciences Understanding
Covers traditional pharmaceutical, rules governing interactions with healthcare professionals, and medical science liaisons and field based medical teams
Regulatory & Compliance
Focuses on ethical and compliance issues relevant to any Medical Affairs professional
Core Technical Competencies
Provides a comprehensive understanding of regulatory affairs, drug development process and more
Medical Science Liaisons and Field Based Medical Teams
Discuss the typical responsibilities of the Medical Science Liaison, as well as the evolution of its specialization to developing and managing relationships between key experts while leveraging expectations by partner companies
Diversity in Clinical Trials
Provides a better understanding of the current state of diversity in clinical trials, its causes and potential solutions
Master These Skills
Drug Development
Clinical Research
Pharmaceutical Industry
Compliance
MSL Best Practices
Engaging KOLs
Regulatory Affairs
Lifecycle Management
Health Care Providers
All ACMA certifications are accredited by IACET/ANSI
25k+
Users
80+
Countries
250+
Companies
Module Breakdown
Module 1
Pharmaceutical Industry Overview
Module 1 explores the pharmaceutical industry’s structure and operations, the divisions within pharmaceutical companies, and the external factors governing the industry.
Module 2
Rules Governing Interactions with Healthcare Professionals
Module 2 explains in detail how the interactions between life sciences companies and healthcare providers - and the regulations governing those interactions - benefit the companies, providers, patient populations and the healthcare system in general.
Module 3
Regulatory Affairs
Module 3 is an overview of the regulatory affairs function within life sciences organizations, both domestically and internationally.
Module 4
Compliance
Module 4 provides pharmaceutical industry compliance rules, regulations, and functions within a pharmaceutical, biotech, medical device, or diagnostics company for both drug and device products.
Module 5
Drug Development Process
Module 5 presents an in-depth explanation of how a compound evolves from the initial discovery stage to the marketplace, detailing the requirements for each phase in the development cycle.
Customer Reviews
4.7 | (500 + Graduates)
Value For Money
4.8/5
Easy to Navigate
4.6/5
Program Content
4.9/5
MACC Credential Value
4.8/5
Reviews Mention
Perfect resource
competitive edge
attracted recruiters
packed with information
Neil Gillette, PharmD, BCMAS
The program was easy to follow and informative. It helped me to better understand the industry as a whole and the opportunities to grow in that field.
Annie Bouchard
The program was very informative and provided an excellent perspective. In addition, it complemented and confirmed my acquired knowledge in the Medical Affairs environment.
Gianluca Stivale, BCMAS
It is an enriching Medical Affairs program with extremely positive impact on daily job
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