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. The Prior Authorization Process
  40. The Pharmaceutical Industry Overview
  41. The Pharmaceutical Industry Overview
  42. Properly Using Guidelines from Insurance Plan
  43. Fundamental Information Before the Authorization Process
  44. The Authorization Process
  45. Fundamentals of Clinical Development
  46. Understanding Medical Evidence
  47. Regulatory & Compliance Rules Influencing the Pharmaceutical Industry
  48. The Medical Devices Industry & Overview
  49. Understanding Medical Terminology
  50. Drug Development & the Pharmaceutical Industry
  51. Drug Development & the Pharmaceutical Industry
  52. Drug Research Post Commercialization
  53. Drug Research Post Commercialization
  54. Pharmacological Fundamentals
  55. Pharmacological Fundamentals
  56. Risk Evaluation and Mitigation Strategies (REMS)
  57. Compliant Interactions with Health Care Providers
  58. The Future of Prior Authorizations (PAs) and Job Opportunities
  59. Publication Practices
  60. The Role of Drugs on Human Physiology
  61. Principles of Pharmacoeconomics
  62. Regulatory & Compliance Rules Influencing the Pharmaceutical Industry
  63. Medical Device Industry
  64. Principles of Pharmacoeconomics
  65. The Medical Devices Industry & Overview
  66. Medical Device Industry
  67. Medical Device Industry
  68. Phase IV/Post-Marketing Studies
  69. Understanding Medical Terminology
  70. Diagnostics Industry
  71. Diagnostics Industry
  72. Rules Governing Interactions with Healthcare Professionals
  73. Rules Governing Interactions with Healthcare Professionals
  74. Rules Governing Interactions with Healthcare Professionals
  75. Health Economics Outcomes Research
  76. Health Economics Outcomes Research
  77. Evidence Based Medicine
  78. Evidence Based Medicine
  79. Evidence Based Medicine
  80. Presentation & Communication Skills
  81. Presentation & Communication Skills
  82. Presentation & Communication Skills
  83. Regulatory Affairs
  84. Regulatory Affairs
  85. Compliance
  86. Compliance
  87. Compliance
  88. Drug Development Process
  89. Drug Development Process
  90. Drug Development Process
  91. Medical Science Liaisons & Field Based Medical Teams
  92. Medical Science Liaisons & Field Based Medical Teams
  93. Medical Science Liaisons & Field Based Medical Teams
  94. Grant & Investigator Initiated Study Funding and Process
  95. Grant & Investigator Initiated Study Funding and Process
  96. Grant & Investigator Initiated Study Funding and Process
  97. Phase IV/Post-Marketing Studies
  98. Insurance Policies
  99. Understanding Types of Clinical Trials
  100. Authorization Denials and Appeals
  101. Fraud & Abuse in the Pharmaceutical Industry
  102. Medical Science Liaisons & Field Based Medical Teams
  103. Risk Evaluation and Mitigation Strategies (REMS)
  104. Compliant Interactions with Health Care Providers
  105. Advisory Boards
  106. Advisory Boards
  107. Advisory Boards
  108. Post-Approval Studies
  109. Risk Evaluation and Mitigation Strategies (REMS)
  110. Risk Evaluation and Mitigation Strategies (REMS)
  111. Risk Evaluation and Mitigation Strategies (REMS)
  112. Interpreting Clinical Papers

Our Authors

 ACMA Instructor