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KOL Speaker Certificate (KSC) Program
Certification Program
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Accredited by IACET/ANSI
The KOL Speaker Certificate program is intended for those healthcare professionals (HCPs) that have been requested by pharmaceutical/biotech companies as speakers to educate the medical community on their products & disease state. The KOL speaker certificate program is an accredited program and provides an overview of all facets that are important for any HCP speaker to be aware of before engaging in a consultancy or speaker engagement with a pharmaceutical company to minimize risk and enhance compliance.
4.3 | (500 + Graduates)
$1199.99
7 Modules
6 Months Access
100% Online & Self Paced
24/7 Live Chat
Frequently Bought Together
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Total Price : $4198.98
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Buy all together : $ 4198.98
Learning Objectives
Industry Insights and Understanding
Helps HCPs gain a comprehensive understanding of the pharmaceutical industry’s structure, key operations, and divisions, including how external regulations, compliance, and policies that govern the industry.
Regulatory, Compliance, and Ethical Expertise
Navigate the ethical and compliance landscape to ensure adherence to industry regulations and standards.
Scientific Story Telling and Technical Mastery
Deliver compelling presentations, communicate complex scientific data effectively, and provide strategic insights to both scientific and non-scientific audiences.
Core Technical Competencies
In-depth industry learning on drug development processes, clinical trial design, and how to communicate scientific information compliantly to internal and external stakeholders.
Master These Skills
Communication skills
Pharmaceutical industry overview
Governing regulations
Regulatory affairs
Compliance rules
Presentation skills
Drug development
Field based medical teams
Clinical trials
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 Expert Program
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.
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