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UNITED STATES OF AMERICA BEFORE FEDERAL TRADE COMMISSION COMMISSIONERS:Timothy J. Maris, Chairman Sheila F. Anthony Moselle W. Thompson Orson Swindle Thomas B. Lorain the Matter of Bristol Myers Squibb
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01
Contact Bristol-Myers Squibb to request a copy of the consent agreement form.
02
Read the consent agreement form carefully and make sure to understand all the terms and conditions.
03
Fill out the form accurately and completely, providing all the required information.
04
Sign and date the form where indicated.
05
Make a copy of the completed form for your records before submitting it to Bristol-Myers Squibb.

Who needs bristol-myers squibb consent agreement?

01
Patients who are participating in a clinical trial sponsored by Bristol-Myers Squibb.
02
Healthcare providers who are involved in the treatment and care of patients enrolled in Bristol-Myers Squibb clinical trials.
03
Research organizations or institutions collaborating with Bristol-Myers Squibb on research projects.
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Bristol-Myers Squibb consent agreement is a legal document that outlines the terms and conditions for consent by the company to allow certain actions or transactions.
Any individual or entity engaging in activities that require approval from Bristol-Myers Squibb may be required to file a consent agreement.
Bristol-Myers Squibb consent agreement can typically be filled out by providing relevant information about the proposed actions or transactions, along with any supporting documentation.
The purpose of Bristol-Myers Squibb consent agreement is to ensure that all parties involved are aware of and agree to the terms and conditions of the proposed actions or transactions.
Information reported on Bristol-Myers Squibb consent agreement may include details about the parties involved, the nature of the proposed actions or transactions, and any relevant dates or deadlines.
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