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Please use the form below. Your message is important to us and will be reviewed by the appropriate team within Pfizer.

Please note that this form is for submitting partnering opportunities to Pfizer’s business development group. This form should not be used for reporting adverse events, submitting resumes, seeking vendor or supplier contacts, etc. There are other areas of the www.pfizer.com website that should be used for each of these specific topics. Thank you for your understanding.

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By submitting this proposal to Pfizer, I represent and warrant that I have the authority to disclose this information to Pfizer.  I acknowledge that I make this submission voluntarily.  I agree that no relationship is established or implied by Pfizer’s acceptance or evaluation of the submitted material, and that Pfizer shall have the right to retain this proposal and submitted material if it chooses to do so.  Pfizer shall not be obligated to specify the reasons for any decision it makes regarding the idea or to reveal any past or present activities that relate to the idea. 

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This form is for submitting partnering opportunities to our business development group only.

We read all messages. However, you may not receive a personal reply due to the large volume of messages we receive.

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Customer Service and Product Inquiries:
1-800-TRY-FIRST (1-800-879-3477)
Monday through Friday 9:00 a.m. to 7:00 p.m. EST

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(212) 733-2323
235 East 42nd Street New York, NY 10017

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Find Answers in our FAQ

You may report an adverse event related to Pfizer products by calling 1-800-438-1985 (U.S. only). If you prefer, you may contact the U.S. Food & Drug Administration (FDA) directly.

The FDA has established a reporting service known as MedWatch through which healthcare professionals and consumers can report serious problems they suspect may be associated with the drugs and medical devices they prescribe, dispense, or use. Visit MedWatch at www.fda.gov/Safety/MedWatch or call 1-800-FDA-1088.

Outside the United States

Countries worldwide may have specific processes in place to handle reports of adverse events. To report an adverse event, ask your health care provider for more information or contact your local health authority.

To learn more about medicine safety, visit our Medicine Safety page.

Go to Medicine Safety