Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial

Instructor: Madhavi Diwanji
Product ID: 701980
  • Duration: 90 Min
This Clinical trial auditing training will provide an understanding of how to conduct compliant and successful clinical trials by defining FDA clinical trial audit procedures, audit program, audit planning and audit preparation.

recorded version

1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Jul-2012

Training CD / USB Drive

One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-362-2367


Read Frequently Asked Questions

Course "Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial" has been pre-approved by RAPS as eligible for up to 1.5 RAC credits towards a participant's RAC recertification upon full completion.

Why Should You Attend:

The field of GCP has rapidly evolved over the last few years and the requirements are getting tougher. Many companies find themselves unprepared for a clinical trial audit, either at a clinical site or their headquarters.

This course will help you to prepare early and help to prevent surprises when being audited. Learn to identify risks and handle them to build a more compliant and successful trial.

This training will also share the ”audit experience”, by sharing what auditors look for and how to prepare for the visit. Define expectations, train your staff and hold them accountable and the inspection will be easy to manage. We will describe proactive measures you can take to assure that all systems are in place, operating well and operating in compliance.

Areas Covered in the Seminar:

  • What is clinical Audit?
  • Audit Vs. Research.
  • The Audit Cycle.
  • Five stages of Clinical Audit.
  • QA Program factors- implementing a program in place.
  • What are the risks?
  • What a sponsor and investigator need to know about FDA audit?
  • Interactive case study to learn about audits.
  • Tips for a successful study.
  • Preparing for a site visit.
  • Most common FDA violations/actions.

Who Will Benefit:

This webinar will provide valuable assistance to all companies/employees (research sites, Clinical research organization, pharmaceutical and biotech industries) that conduct clinical trials.

  • Regulatory Affairs
  • Clinical Trial staff and management
  • Clinical Development
  • Project Managers
  • Drug Safety staff

Instructor Profile:

Madhavi Diwanji, MBA, CCRC is the President of MD Clinical Monitor. She has tremendous experience in the healthcare industry in various roles for the past 20 years. She is well rounded in all aspects of clinical trial as she has been instrumental in healthcare research with a primary focus on cardiology and oncology. She has experience with monitoring clinical trials, conducting clinical trials, investigator initiated trials, maintaining multiple Trial Master Files, starting a research program in a hospital, health services research, regulatory /compliance submission and management, grant submission, business development and fundraising. She has successfully worked with different IRBs, CROs and sponsors. She has served on a study coordinator advisory committee of a global Congestive Heart failure clinical trial. She currently consults with helping clinical research departments in need services like starting up, regulatory, closing down and increasing productivity.

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Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email call +1-888-717-2436 (Toll Free).

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