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pyrvinium

As the list published 23 Sept 2026 has it, binding since 23 Apr 2025. Each entry binds six months after its own publication date (Article 107c(7) of Directive 2001/83/EC).

What the list says

EU reference date
Not stated
PSUR frequency
10 years
Data lock point
3 Nov 2036
Submission date
1 Feb 2037
Next data lock point
Not stated
Next submission date
Not stated
Products covered
Nationally authorised (NAP)

Are PSURs required for products referred to in Articles 10(1), 10a and 16a of Directive 2001/83/EC?

No — the list does not require PSURs for these products.

The list asks this as one question for Articles 10(1), 10a and 16a together, and does not answer it for Article 14 at all. A PSUR may in any case be required at the request of a competent authority or as a condition of the marketing authorisation.

Notes in the list

PSUR frequency and DLP amended on 23/10/2024

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The next three reports

  • Data lock point 3 Nov 2036Submission by 1 Feb 2037
  • Data lock point 3 Nov 2046Submission by 1 Feb 2047
  • Data lock point 3 Nov 2056Submission by 1 Feb 2057

Counted from the data lock point the list gives, on the cycle it states: the submission date is 90 days after the data lock point — 70 days for a cycle of twelve months or less, 90 days for a longer one, as GVP Module VII sets out.

In earlier versions of the list

  • EMA/630645/2012 Rev.164 · published 23 Sept 2026

    pyrvinium — every 10 years, data lock point 3 Nov 2036

  • EMA/630645/2012 Rev.156 · published 4 Feb 2026

    pyrvinium — every 10 years, data lock point 3 Nov 2036

Source: European Medicines Agency, list of EU reference dates and frequency of submission of periodic safety update reports, EMA/630645/2012 Rev.164, published 23 Sept 2026. Open the published file

Kreastel is a planning and oversight aid for pharmacovigilance obligations. It tracks dates like these for a marketing authorisation holder's own products.

Report a discrepancy — if this page and the published file disagree, the file is right and we want to know.

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