Proposed Best Practice Guidelines for Scientific Response Documents: A Consensus Statement from phactMI

Author:

Hermes-DeSantis Evelyn R.,Johnson Renee M.,Redlich Alysa,Patel Bindi,Flanigan-Minnick Anne,Wnorowski Susan,Cortes Mabel M.,Han Chang Woo,Vine Elissa,Sarwar Hamza,Haydar Rita,Jamil Ahsan,Huang Tiffany,Sandhu Sonia Kaur,Reilly Patrick

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Public Health, Environmental and Occupational Health,Pharmacology, Toxicology and Pharmaceutics (miscellaneous)

Reference17 articles.

1. Guidance for Industry - Responding to Unsolicited Requests for Off-Label Information About Prescription Drugs and Medical Devices - DRAFT GUIDANCE. US Food and Drug Administration. (2011 December). https://www.fda.gov/regulatory-information/search-fda-guidance-documents/responding-unsolicited-requests-label-information-about-prescription-drugs-and-medical-devices. Accessed 30 Aug 2019.

2. Albano D, Ferri S. A proposal to replace “SRL” as the common term for medical information response documents. Ther Innov Reg Sci. 2018;52:403–4. https://doi.org/10.1177/2168479018759663.

3. phactMI [Internet] West Point, PA: c2019. Code of Practice [about 1 screen]. https://www.phactmi.org/PortalCodeOfPractice. Accessed 30 Aug 2019.

4. Lau V. Study: One-third of docs trust pharma content on HCP sites. MM&M May 18, 2017. https://www.mmm-online.com/home/channel/media-news/study-one-third-of-docs-trust-pharma-content-on-hcp-sites/. Accessed 24 Feb 2020.

5. Manhattan Research. ePharma Physician® 2015 Survey. New York, NY.

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