Fraud in Clinical Research

Instructor: David Lim 
Product ID: 703899
  • Duration: 60 Min

recorded version

1x Person - Unlimited viewing for 6 Months
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Recorded Link and Ref. material will be available in My CO Section

Training CD

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Read Frequently Asked Questions

This training program will instruct attendees to better understand ethical and legal requirements when conducting medical/clinical research and study. The webinar will focus on what/how to identify, address and prevent fraud in medical research.

Why Should You Attend:

Fraud in medical research has a long, documented history. This webinar will discuss fraud in medical research to greatly improve attendees’ awareness about recent fraud in medical study and research. In particular, it is intended to help industry understand ethical and legal requirements when conducting medical research. The speaker will discuss key issues from recent cases of fraud in medical research and clinical trials.

The speaker will also share what should be done to properly address and rather prevent fraud in medical/clinical research and study including Dos and Don’ts. At the end of the webinar, participants will become familiar with the issues in fraud so that you can proactively identify, address and prevent fraud in medical/clinical research.

Learning Objectives:

  • To be better aware of instances of fraud in medical research
  • How to address and prevent fraud

Areas Covered in the Webinar:

  • Laws and Regulations
  • Regulatory Requirements
  • Code of Conduct for Medical Research
  • Recent Fraud Cases in Medical/Clinical Research/Clinical Trials
  • Duties, Responsibilities and Roles of the Stakeholders including FDA
  • Motives for Fraud
  • Recent Deadly-Ego Driven Games
  • Deadly Corruption in Clinical Research
  • How to Address Fraud in Medical/Clinical Research
  • How to Prevent Fraud
  • PASS-IT Recommendations

Who Will Benefit:

This webinar will benefit those working with global pharmaceuticals, medical device and IVDs, healthcare industry, compliance consulting firms, health authorities, and compliance, regulatory, marketing and sales professionals.

  • Senior Management
  • Compliance Officers
  • Attorneys
  • Regulatory Affairs
  • Clinical Affairs
  • Quality Assurance
  • R&D
  • University Officials and Researchers
  • Consultants
  • Contractors/Subcontractors
  • Anyone interested in the topic

Instructor Profile:

Dr. David Lim, Ph.D., RAC, ASQ-CQA, is president and principal of Regulatory Doctor. He frequently presents global regulatory and quality compliance topics in various forums and meetings. Recently, Dr. Lim developed 510(k) templates ready for use compliant with e-Copy and RTA policy. In addition, he developed FDA inspection checklists for drug and medical device manufacturers based on his analysis of FDA inspectional observations cited in 483s for the past eight years. Dr. Lim provides his feedback to regulatory agencies (e.g., US FDA) through public comments and also served as a panel member during the FDA’s transparency public meeting in 2009. He contributes to the Regulatory Affairs Professional Society (RAPS) as an author and speaker. Dr. Lim leads and directs all research projects including, but not limited to, pharmacovigilance, medical device reporting, recalls and patient safety signals being conducted at the Regulatory Doctor. He serves as a member of the Advisory Board for Inspection Insider published by FDA News.

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