Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comment
. 2018 Nov 15;16(1):98.
doi: 10.1186/s12961-018-0371-4.

Regulatory scientists' work has important ramifications for public health and should be open to public scrutiny

Affiliations
Comment

Regulatory scientists' work has important ramifications for public health and should be open to public scrutiny

Shai Mulinari et al. Health Res Policy Syst. .

Abstract

The Swedish Medical Products Agency (MPA) objects to the fact that we occasionally refer to one of its senior ex-employees by name. However, names of individual MPA assessors, Food and Drug Administration (FDA) reviewers, and European Medicines Agency rapporteurs and co-rapporteurs are cited in regulatory documents and are a matter of public record. In our paper (Health Res Policy Syst 15:93, 2017), we in no way suggest that regulatory decisions were left to individual reviewers or assessors, although we do emphasise that individual MPA and FDA employees' scientific assessments and benefit-risk evaluations are critical to the decision-making process. In this response to the MPA, we raise a further issue - one in which the question of personal identification of individuals is relevant - and this pertains to the accountability of influential scientists and experts who contribute to public policy decisions with important ramifications for public health. In our view, it is important that interested observers are able to identify those influential individuals, and entirely appropriate that their work should be open to public scrutiny.

PubMed Disclaimer

Conflict of interest statement

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Comment on

Similar articles

Cited by

References

    1. Andersson Forsman C. The Swedish Medical Products Agency’s rules of procedure. Health Res Policy Syst. 2018. 10.1186/s12961-018-0372-3. - PMC - PubMed
    1. Mulinari S, Davis C. Why European and United States drug regulators are not speaking with one voice on anti-influenza drugs: regulatory review methodologies and the importance of ‘deep’ product reviews. Health Res Policy Syst. 2017;15:93. doi: 10.1186/s12961-017-0259-8. - DOI - PMC - PubMed
    1. European Medicines Agency . EuroPasss: Ingrid Uhnoo 26/3/18. 2018.
    1. Uhnoo I, Linde A, Pauksens K, Lindberg A, Eriksson M, Norrby R. Treatment and prevention of influenza: Swedish recommendations. Scand J Infect Dis. 2003;35(1):3–11. doi: 10.1080/0036554021000026999. - DOI - PubMed
    1. Uhnoo I, Linde A. Antiviral agents in influenza - current recommendations. Anti-influenza agents are not a substitution for but a complement to vaccination [Article in Swedish] Swedish Med J. 2005;102(49):3802–3803. - PubMed

Substances