Sissetulev dokumentAvalik
Selgitustaotlus
Terviseamet · 6. mai 2026
- Viit
- 10.1-5/26/276-1
- Registreeritud
- 6. mai 2026
- Dokumendi liik
- Sissetulev dokument
- Adressaat
- Yordas Grupp
- Saabumis/saatmisviis
- e-post
- Funktsioon
- 10.1 Kemikaaliohutusega seotud toimingud
- Sari
- 10.1-5 Biotsiidide käitlemist Eestis ja EL õigusruumis puudutav kirjavahetus, info- ja muud dokumendid
- Toimik
- 10.1-5/2026
- Vastutaja
- Riina Lahne (TA, Peadirektori asetäitja (1) vastutusvaldkond, Kemikaaliohutuse osakond)
- Lahendamise tähtaeg
- 21. mai 2026
Failid
Sisu (failidest)
Saatja: "Adam Thickett" <[email protected]>
Saaja: [email protected]
Teema: Applications under BPR Transitional Rules
Kuupäev: 2026-05-05 15:47
Tähelepanu! Tegemist on väljastpoolt asutust saabunud kirjaga. Tundmatu
saatja korral palume linke ja faile mitte avada.
To whom it may concern,
We are working with a client who is interested in registering a biocidal
product under Estonian transitional regulations. The active substances are
currently under evaluation for approval within the EU BPR Review Programme
but we have one question we would like to understand before we proceed with
preparing the application form.
If aa product contains active substances which have been granted an approval
decision by the BPC but for which the active substance approval start date
has not yet been reached, can the applicant still seek an approval to market
under Estonian transitional rules? If so, is there a deadline before the
approval start date to submit these applications or can this be done up to
the approval start date (providing a BPR authorisation application is also
submitted prior to this date for the same product)?
We would appreciate any information you can provide in this regard to help
with our clients decision making.
Many thanks and best regards.
Adam Savins Thickett (He/Him)
Regulatory Consultant
Yordas Group
My working days are Mon-Fri
t: +441612506199
e: <mailto:[email protected]> [email protected]
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