SFDA item 74 · IV. PMF/VAMF
Deletion or change of status (operational/non-operational) of establishment(s)/centre(s) used for blood/plasma collection or in the for testing donations and plasma pools.
Variation category under SFDA, EU and US FDA rules for this change, with the variant wording as published.
SFDA Saudi Food and Drug Authority
Guidelines for Variation Requirements v6.3 (DS-G-006), item 74 — official PDF, p. 74 ↗
| Variant | Change | Type |
|---|---|---|
| - | Deletion or change of status (operational/non-operational) of establishment(s)/centre(s) used for blood/plasma collection or in the for testing donations and plasma pools. | Type IA |
Conditions to be fulfilled and documentation to be supplied: see the official guideline, item 74.
EU European Union
Commission Guidelines C/2025/5045 — EUR-Lex ↗
M.5 · Deletion or change of status (operational/non-operational) of establishment(s)/centre(s) used for blood/plasma collection or in the testing of donations and plasma pools
| Variant | Change | Type |
|---|---|---|
| 1 | Deletion | Type IA |
| 2.a | Change of status — from operational to non-operational | Type IA |
| 2.b | Change of status — from non-operational to operational | Type IA |
| 2.c | Change of status — from non-operational to operational when epidemiological data has not been annually submitted or there have been other than administrative changes in blood establishment or centres since there were moved to non-operational (e.g. blood bags, testing kits) | Type IB |
US FDA US Food and Drug Administration
21 CFR 314.70 and FDA guidance — Outside 21 CFR 314.70 — CBER establishment licensing, 21 CFR 601.12, 607
| Change | Category | Reference |
|---|---|---|
| Handled under the establishment's own registration/CBER license | No US equivalent |
Note: Collection and testing facilities are managed under the establishments' CBER licenses and FDA registration (21 CFR 601.12, 607); no PMF variation exists.
Other items in IV. PMF/VAMF
- 1 · Change in the marketing authorization holder
- 2 · Remove agent name from the artwork (Mock-up)
- 3 · Change in the (invented) name of the medicinal product
- 4 · Change in name of the active substance
- 5 · Change in the name and/or address of a manufacturer or supplier of the active substance, starting material, reagent or intermediate used in the manufacture of the active substance (where specified in the product dossier) where no Certificate of Suitability is available
- 6 · Change in the name and/or address of a manufacturer of the finished product, including quality control sites
- 7 · Change in ATC Code /ATC Vet Code
- 8 · Deletion of a manufacturing sites (including for an active substance, intermediate or finished product, packaging site, manufacturer responsible for batch release, site where batch control takes place, or supplier of a starting material, reagent or excipient, when mentioned in the dossier).
- 55 · Change in the summary of product characteristics, labeling and patient information leaflet of a generic/hybrid/biosimilar medicinal product following assessment of the same change for the reference product *.
- 56 · Change(s) in the summary of product characteristics, labeling and patient information leaflet related to post authorization safety study (PASS), periodic safety update report, risk management plan or SFDA drug safety monitoring activities.
- 57 · Variations related to significant modifications of the Summary of Product Characteristics due in particular to new quality, pre-clinical, clinical or pharmacovigilance data*
- 58 · Change(s) to therapeutic indication(s)
Not regulatory advice. The binding text is each regulator's current official document; confirm the category with the authority before filing. FDA publishes no classification table: the US category follows FDA guidance or, where the guidance does not name the change, the closest example under 21 CFR 314.70.