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BERIPLEX AU human prothrombin complex 500 IU powder for injection vial, CSL Behring Australia Pty Ltd, CON-1251

Product name
BERIPLEX AU human prothrombin complex 500 IU powder for injection vial
Sponsor name
CSL Behring Australia Pty Ltd
ARTG details
  • 328515)
Consent start
Consent no.
CON-1251
Duration
The consent is effective from 28 June 2024 until 1 October 2031.
Standard
Part 2 Section 10(9) and Schedule 1 Item 8(b), Item 8(c);
Part 2 Section 10(4) Schedule 1 Item 10(d);
Part 2 Section 10(4) Schedule 1 Item 10(c) of Therapeutic Goods (Standard for Human Cell and Tissue Products - Donor Selection Requirements) (TGO 108) Order 2021
Non-compliance with standard
The products will not comply with: - the requirement of indefinite geographical deferral for variant Creutzfeldt-Jakob disease (vCJD) risk, applicable to blood and plasma donors having spent a cumulative length of time of 6 months or more in the UK between 1980 and 1996 or receiving a transfusion or injection of blood or blood components while in the UK at any time on or after 1 January 1980. - Donor selection criteria for deferral following body piercing - where single-use equipment is used, and it is less than 4 months since the procedure and where the person tests negative for HCV using NAT - Donor selection criteria for deferral following tattoo - in that people who have a tattoo performed at a licensed/registered tattoo parlour or cosmetic clinic in Australia can be accepted as a donor for plasma for fractionation only with no deferral period from the time of the last tattoo procedure.
Conditions imposed
That the sponsor continues to monitor the literature and informs the TGA of any new evidence that substantively alters the estimated risks, such that they become unacceptable.
Import, Supply, &/or Export
supply
Therapeutic product type
Prescription medicines