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ACMA Instructor
Dr.
Other Online Trainings Provided:
Overview of Medical Information
Diversity in Clinical Trials
Clinical Trial Designs
Abstract & Medical Writing
Grant & Investigator Initiated Study Funding and Process
Clinical Trial Designs
Abstract & Medical Writing
Basic Principles in Pharmacology
Prevention of Prescription Drug Fraud and Abuse
High Value Selling
Analyzing Peer-Reviewed Literature on Pharmacological Treatments
Phase IV/Post-Marketing Studies
Publication Practices
Publication Practices
Health Economics Outcomes Research
Drug Development Process
Overview of Medical Information
Medication Safety & Pharmacovigilance
Medication Safety & Pharmacovigilance
The Pharmaceutical Industry Overview
Regulatory Affairs in Brazil
Overview of Medical Information
Regulatory Affairs in India
The Pharmaceutical Industry Overview
Regulatory Affairs in Asia: Focus on China, Japan, Singa-pore, Hong Kong
Regulatory Affairs Overview in Europe
Anatomical & Physiological Effects of Drugs
Clinical Development Expert Program
The Pharmaceutical Industry Overview
Rules Governing Interactions with Healthcare Professionals
Regulatory Affairs
Medical Terminology & Abbreviations
FDA Laws and Regulations Related to Pharmaceutical Industry Marketing
Principles of Pharmacoeconomics
Introduction to Opioid Use for Pharmaceutical Industry Professionals
Comparison of Therapeutic Drug Classes
Coverage Determination Types in Medication Prior Authorizations
Insurance Policies
Rules Governing Interactions with Healthcare Professionals
The Pharmaceutical Industry Overview
Properly Using Guidelines from Insurance Plan
Service Line, Medication Initiation & Submission of a Prior Authorization
The Authorization Process
Fundamentals of Clinical Development
Out of Network Waivers
Understanding Medical Evidence
Regulatory & Compliance Rules Influencing the Pharmaceutical Industry
The Medical Devices Industry & Overview
Understanding Medical Terminology
Drug Development & the Pharmaceutical Industry
Drug Development & the Pharmaceutical Industry
Drug Research Post Commercialization
Drug Research Post Commercialization
Pharmacological Fundamentals
Pharmacological Fundamentals
Risk Evaluation and Mitigation Strategies (REMS)
Compliant Interactions with Health Care Providers
Authorization Denials and Appeals
The Prior Authorization Process
The Future of Prior Authorizations and Job Opportunities
Medical Records and The Prescription
Rules Governing Interactions with Healthcare Professionals
Health Economics Outcomes Research
Health Economics Outcomes Research
Clinical Trial Designs
Drug Development Process
Evidence Based Medicine
Overview of Medical Information
Medical Science Liaisons & Field Based Medical Teams
Grant & Investigator Initiated Study Funding and Process
Advisory Boards
Presentation & Communication Skills
Phase IV/Post-Marketing Studies
Risk Evaluation and Mitigation Strategies (REMS)
The Pharmaceutical Industry Overview
Medical Device Industry
Compliance
Diagnostics Industry
Rules Governing Interactions with Healthcare Professionals
Evidence Based Medicine
Medication Safety & Pharmacovigilance
Communication Methods of the Prior Authorization
Health Economics Outcomes Research
Drug Development Process
Evidence Based Medicine
Drug Development Process
Overview of Medical Information
Medical Science Liaisons & Field Based Medical Teams
Medical Science Liaisons & Field Based Medical Teams
Grant & Investigator Initiated Study Funding and Process
Advisory Boards
Medication Safety & Pharmacovigilance
Advisory Boards
Fundamental Information Before the Authorization Process
Phase IV/Post-Marketing Studies
Health Economics Outcomes Research
Presentation & Communication Skills
Regulatory Affairs
Risk Evaluation and Mitigation Strategies (REMS)
Rules Governing Interactions with Healthcare Professionals
Compliance
Post-Approval Studies
Risk Evaluation and Mitigation Strategies (REMS)
Overview of Medical Information - Content Only
Medical Science Liaisons & Field Based Medical Teams - Content Only
Phase IV/Post-Marketing Studies - Content Only
Medical Device Industry - Content Only
Diagnostics Industry - Content Only
Health Economics Outcomes Research - Content Only
Grant & Investigator Initiated Study Funding and Process - Content Only
Advisory Boards - Content Only
Healthcare Compliance Attestation
Medical Device Industry
Regulatory Affairs
Overview of Medical Information
Advisory Boards
Compliance
Regulatory Affairs in China
Drug Development Process
Compliance
Abstract & Medical Writing
Publication Practices
Medical Science Liaisons & Field Based Medical Teams
The Pharmaceutical Industry Overview
The Pharmaceutical Industry Overview
Diagnostics Industry
Rules Governing Interactions with Healthcare Professionals
Clinical Trial Designs
Presentation & Communication Skills
Regulatory Affairs
Compliance
Abstract & Medical Writing
Publication Practices
Phase IV/Post-Marketing Studies
PhRMA Code Attestation
Medical Device Industry
Publication Practices
Future of Pharma Industry Careers
Regulatory Affairs
Publication Practices
Risk Evaluation and Mitigation Strategies (REMS)
Diagnostics Industry
Diagnostics Industry
Compliance HIPAA, Security, Fraud and Abuse
The Role of Drugs on Human Physiology
Regulatory Affairs
Grant & Investigator Initiated Study Funding and Process
Risk Evaluation and Mitigation Strategies (REMS)
Medical Device Industry
Rules Governing Interactions with Healthcare Professionals
Health Economics Outcomes Research
Evidence Based Medicine
Clinical Trial Designs
Presentation & Communication Skills
Grant & Investigator Initiated Study Funding and Process
Phase IV/Post-Marketing Studies
Risk Evaluation and Mitigation Strategies (REMS)
Medication Safety & Pharmacovigilance
Diagnostics Industry
Regulatory & Compliance Rules Influencing the Pharmaceutical Industry
Compliance
Principles of Pharmacoeconomics
The Medical Devices Industry & Overview
Medical Device Industry
Medication Safety & Pharmacovigilance
Understanding Medical Terminology
Rules Governing Interactions with Healthcare Professionals
Health Economics Outcomes Research
Evidence Based Medicine
Presentation & Communication Skills
Medical Science Liaisons & Field Based Medical Teams
Grant & Investigator Initiated Study Funding and Process
Medical Device Industry
Understanding Types of Clinical Trials
Diagnostics Industry
Fraud & Abuse in the Pharmaceutical Industry
Medical Device Industry
Health Economics Outcomes Research
Clinical Trial Designs
Compliance
Medical Science Liaisons & Field Based Medical Teams
Grant & Investigator Initiated Study Funding and Process
The Pharmaceutical Industry Overview - Content Only
Rules Governing Interactions with Healthcare Professionals - Content Only
Regulatory Affairs - Content Only
Compliance - Content Only
Abstract & Medical Writing - Content Only
Publication Practices - Content Only
Drug Development Process - Content Only
Clinical Trial Designs
Presentation & Communication Skills
Abstract & Medical Writing
Drug Development Process
Diagnostics Industry
Medical Science Liaisons & Field Based Medical Teams
Risk Evaluation and Mitigation Strategies (REMS)
Compliant Interactions with Health Care Providers
Clinical Trial Designs - Content Only
Presentation & Communication Skills - Content Only
Risk Evaluation and Mitigation Strategies (REMS) - Content Only
Special Considerations for Service Orders
Diagnostics Industry
Evidence Based Medicine
Advisory Boards
The Pharmaceutical Industry Overview
The Pharmaceutical Industry Overview
Diagnostics Industry
Advisory Boards
Presentation & Communication Skills
Medication Safety & Pharmacovigilance - Content Only
Risk Evaluation and Mitigation Strategies (REMS)
Interpreting Clinical Papers
Regulatory Affairs
Regulatory Affairs
Compliance
Evidence Based Medicine
Abstract & Medical Writing
Publication Practices
Abstract & Medical Writing
Publication Practices
Drug Development Process
Overview of Medical Information
Advisory Boards
Phase IV/Post-Marketing Studies
Medication Safety & Pharmacovigilance
Medical Science Liaisons & Field Based Medical Teams
Our Authors
ACMA Instructor