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Comment

. 2017 Apr 12:357:j1851.

doi: 10.1136/bmj.j1851.

Three design aspects for high quality post-marketing cohort studies

Michael Fralick¹, Aaron S Kesselheim¹

Affiliations

Affiliation

¹ Program on Regulation, Therapeutics, and Law (PORTAL), Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02120, USA.

PMID: 28404570
DOI: 10.1136/bmj.j1851

Comment

Three design aspects for high quality post-marketing cohort studies

Michael Fralick et al. BMJ. 2017.

. 2017 Apr 12:357:j1851.

doi: 10.1136/bmj.j1851.

Authors

Michael Fralick¹, Aaron S Kesselheim¹

Affiliation

¹ Program on Regulation, Therapeutics, and Law (PORTAL), Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02120, USA.

PMID: 28404570
DOI: 10.1136/bmj.j1851

No abstract available

PubMed Disclaimer

Comment in

Authors' reply to Fralick and Kesselheim.
Spelsberg A, Keil U, Prugger C. Spelsberg A, et al. BMJ. 2017 Apr 12;357:j1850. doi: 10.1136/bmj.j1850. BMJ. 2017. PMID: 28404584 No abstract available.

Comment on

Contribution of industry funded post-marketing studies to drug safety: survey of notifications submitted to regulatory agencies.
Spelsberg A, Prugger C, Doshi P, Ostrowski K, Witte T, Hüsgen D, Keil U; Working Group on Health and Working Group on Freedom of Information, Transparency International Deutschland eV. Spelsberg A, et al. BMJ. 2017 Feb 7;356:j337. doi: 10.1136/bmj.j337. BMJ. 2017. PMID: 28174182 Free PMC article.

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