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amylase / bromelain / chymotrypsin / lipase / pancreatin / papain / rutoside / trypsin, trypsin/ bromelain/ rutoside trihydrate

As the list published 23 Sept 2026 has it, binding since 12 Mar 2026. 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
9 years
Data lock point
3 Mar 2029
Submission date
1 Jun 2029
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 amended and DLP updated on 28/08/2024

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The next three reports

  • Data lock point 3 Mar 2029Submission by 1 Jun 2029
  • Data lock point 3 Mar 2038Submission by 1 Jun 2038
  • Data lock point 3 Mar 2047Submission by 1 Jun 2047

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

    amylase / bromelain / chymotrypsin / lipase / pancreatin / papain / rutoside / trypsin, trypsin/ bromelain/ rutoside trihydrate — every 9 years, data lock point 3 Mar 2029

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

    amylase / bromelain / chymotrypsin / lipase / pancreatin / papain / rutoside / trypsin, trypsin/ bromelain/ rutoside trihydrate — every 9 years, data lock point 3 Mar 2029

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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