ACMA Instructor Dr.


Other Online Trainings Provided:
  1. Abstract & Medical Writing
  2. Health Economics Outcomes Research
  3. Clinical Trial Designs
  4. Abstract & Medical Writing
  5. Clinical Trial Designs
  6. Clinical Trial Designs
  7. Abstract & Medical Writing
  8. Basic Principles in Pharmacology
  9. Prevention of Prescription Drug Fraud and Abuse
  10. High Value Selling
  11. Analyzing Peer-Reviewed Literature on Pharmacological Treatments
  12. Publication Practices
  13. Publication Practices
  14. Publication Practices
  15. Overview of Medical Information
  16. Diagnostics Industry
  17. Overview of Medical Information
  18. Medication Safety & Pharmacovigilance
  19. Medication Safety & Pharmacovigilance
  20. Medication Safety & Pharmacovigilance
  21. Regulatory Affairs in Brazil
  22. Overview of Medical Information
  23. Regulatory Affairs in India
  24. The Pharmaceutical Industry Overview
  25. Future of Pharma Industry Careers
  26. Regulatory Affairs in Asia: Focus on China, Japan, Singa-pore, Hong Kong
  27. Regulatory Affairs Overview in Europe
  28. Anatomical & Physiological Effects of Drugs
  29. Clinical Development Expert Program
  30. The Pharmaceutical Industry Overview
  31. Rules Governing Interactions with Healthcare Professionals
  32. Regulatory Affairs
  33. Medical Terminology & Abbreviations
  34. FDA Laws and Regulations Related to Pharmaceutical Industry Marketing
  35. Principles of Pharmacoeconomics
  36. Introduction to Opioid Use for Pharmaceutical Industry Professionals
  37. Comparison of Therapeutic Drug Classes
  38. Coverage Determination Types in Medication Prior Authorizations
  39. Insurance Policies
  40. The Pharmaceutical Industry Overview
  41. The Pharmaceutical Industry Overview
  42. Properly Using Guidelines from Insurance Plan
  43. Outpatient Services
  44. The Authorization Process
  45. Fundamentals of Clinical Development
  46. Out of Network Waivers
  47. Understanding Medical Evidence
  48. Regulatory & Compliance Rules Influencing the Pharmaceutical Industry
  49. The Medical Devices Industry & Overview
  50. Understanding Medical Terminology
  51. Drug Development & the Pharmaceutical Industry
  52. Drug Development & the Pharmaceutical Industry
  53. Drug Research Post Commercialization
  54. Drug Research Post Commercialization
  55. Pharmacological Fundamentals
  56. Pharmacological Fundamentals
  57. Risk Evaluation and Mitigation Strategies (REMS)
  58. Compliant Interactions with Health Care Providers
  59. Authorization Denials and Appeals
  60. The Prior Authorization Process
  61. The Future of Prior Authorizations and Job Opportunities
  62. Medical Records and The Prescription
  63. Rules Governing Interactions with Healthcare Professionals
  64. Health Economics Outcomes Research
  65. Health Economics Outcomes Research
  66. Clinical Trial Designs
  67. Drug Development Process
  68. Evidence Based Medicine
  69. Overview of Medical Information
  70. Medical Science Liaisons & Field Based Medical Teams
  71. Grant & Investigator Initiated Study Funding and Process
  72. Advisory Boards
  73. Presentation & Communication Skills
  74. Phase IV/Post-Marketing Studies
  75. Risk Evaluation and Mitigation Strategies (REMS)
  76. The Pharmaceutical Industry Overview
  77. Medical Device Industry
  78. Compliance
  79. Diagnostics Industry
  80. Rules Governing Interactions with Healthcare Professionals
  81. Evidence Based Medicine
  82. Medication Safety & Pharmacovigilance
  83. Drug Development Process
  84. Medical Science Liaisons & Field Based Medical Teams
  85. Grant & Investigator Initiated Study Funding and Process
  86. Advisory Boards
  87. Phase IV/Post-Marketing Studies
  88. Publication Practices
  89. Communication Methods of the Prior Authorization
  90. Service Line, Medication Initiation & Submission of a Prior Authorization
  91. Compliance HIPAA, Security, Fraud and Abuse
  92. The Role of Drugs on Human Physiology
  93. Fundamental Information Before the Authorization Process
  94. Principles of Pharmacoeconomics
  95. Regulatory & Compliance Rules Influencing the Pharmaceutical Industry
  96. Medical Device Industry
  97. Principles of Pharmacoeconomics
  98. The Medical Devices Industry & Overview
  99. Medical Device Industry
  100. Medical Device Industry
  101. Phase IV/Post-Marketing Studies
  102. Understanding Medical Terminology
  103. Diagnostics Industry
  104. Rules Governing Interactions with Healthcare Professionals
  105. Rules Governing Interactions with Healthcare Professionals
  106. Health Economics Outcomes Research
  107. Evidence Based Medicine
  108. Evidence Based Medicine
  109. Presentation & Communication Skills
  110. Presentation & Communication Skills
  111. Regulatory Affairs
  112. Regulatory Affairs
  113. Compliance
  114. Compliance
  115. Drug Development Process
  116. Drug Development Process
  117. Medical Science Liaisons & Field Based Medical Teams
  118. Medical Science Liaisons & Field Based Medical Teams
  119. Grant & Investigator Initiated Study Funding and Process
  120. Grant & Investigator Initiated Study Funding and Process
  121. Understanding Types of Clinical Trials
  122. Fraud & Abuse in the Pharmaceutical Industry
  123. Medical Science Liaisons & Field Based Medical Teams
  124. Risk Evaluation and Mitigation Strategies (REMS)
  125. Compliant Interactions with Health Care Providers
  126. Diagnostics Industry
  127. Advisory Boards
  128. Advisory Boards
  129. Presentation & Communication Skills
  130. Post-Approval Studies
  131. Risk Evaluation and Mitigation Strategies (REMS)
  132. Risk Evaluation and Mitigation Strategies (REMS)
  133. Risk Evaluation and Mitigation Strategies (REMS)
  134. Interpreting Clinical Papers
  135. Regulatory Affairs
  136. Regulatory Affairs
  137. Compliance
  138. Abstract & Medical Writing
  139. Publication Practices

Our Authors

 ACMA Instructor