Medtech Insight is part of Pharma Intelligence UK Limited

This site is operated by Pharma Intelligence UK Limited, a company registered in England and Wales with company number 13787459 whose registered office is 5 Howick Place, London SW1P 1WG. The Pharma Intelligence group is owned by Caerus Topco S.à r.l. and all copyright resides with the group.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction

CLINICAL INVESTIGATOR INDEPENDENCE CERTIFICATION BEING CONSIDERED BY FDA

This article was originally published in The Gray Sheet

Executive Summary

Sponsor certification of clinical investigator independence is one approach under consideration by FDA to address conflict-of- interest concerns. FDA will float the certification idea in a draft policy to be issued later this year. FDA proposed the idea of certification in a draft response to a May 27 letter on financial disclosure sent to FDA Commissioner David Kessler by House Small Business regulation subcommittee Chairman Ronald Wyden (D-Ore.). The subcommittee held a hearing on conflict-of-interest issues on June 17 (see related item, In Brief). Under the proposed policy, sponsors would have the option of certifying the financial independence of clinical investigators or fully disclosing any financial relationship the clinician has with the company. In his letter to the commissioner, Wyden suggested that "some disclosure of those financial ties, and the conflicts-of-interest, be made to [FDA] at the time trial information is evaluated." He added that "a little sunlight may be the best possible disinfectant in such conflict-of-interest matters." FDA held a series of meetings beginning in late March with consumer representatives, physician associations and regulated industry, including the Health Industry Manufacturers Association, on financial disclosure by clinical investigators. In a background paper prepared for the meetings, FDA states that it "believes that there are potential sources of bias that may directly or indirectly influence the outcomes of research." The agency cites certain checks and balances currently included in the evaluation process, including its bioresearch monitoring program, but notes that "no information is available to the agency with respect to financial holdings of clinical investigators." FDA asked the meeting attendees for advice on a number of points, including whether it should require the submission of information on financial interests, at what point during the review process the financial information should be disclosed and information on the ways in which sponsors compensate investigators.

Latest Headlines
See All
UsernamePublicRestriction

Register

MT000762

Ask The Analyst

Ask the Analyst is free for subscribers.  Submit your question and one of our analysts will be in touch.

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel