COMMONWEALTH OF AUSTRALIA
Department of Health
Therapeutic Goods Administration
THERAPEUTIC GOODS ACT 1989
PUBLICATION OF LIST OF MANUFACTURERS REVOKED FROM LICENSING FOR
THE MANUFACTURE OF THERAPEUTIC GOODS
I, David Rowbury, Delegate of the Secretary of the Department of Health, Therapeutic Goods Administration for the purpose of section 41 of the Therapeutic Goods Act 1989, hereby publish the following details concerning the revocation of a Licence to Manufacture Therapeutic Goods:
Under section 41(1)(d) of the Therapeutic Goods Act 1989 the Secretary by notice in writing has revoked the Licence held by:
PlusLife – LICENCE NO. MI-25052005-LI-000576-2 OF Perth Orthopaedic Institute, Gate 3, Verdun Street, Hollywood Hospital, NEDLANDS, WA, 6909 – AT THE REQUEST OF THE MANUFACTURER.
Eurofins ams Laboratories Pty Ltd – LICENCE NO. MI-2013-LI-07582-1 OF 2/120 Bluestone Circuit, SEVENTEEN MILE ROCKS, QLD, 4073 – AT THE REQUEST OF THE MANUFACTURER.
The Pharmaceutical Plant Company Pty Ltd – LICENCE NO. MI-10012005-LI-000349-2 OF 24 London Drive, BAYSWATER NORTH, VIC, 3153 – AT THE REQUEST OF THE MANUFACTURER.
Pfizer Australia Pty Ltd – LICENCE NO. MI-10022005-LI-000433-1 OF 38-42 Wharf Rd, WEST RYDE, NSW, 2114 – AT THE REQUEST OF THE MANUFACTURER.
Eris Pharmaceuticals (Australia) Pty Ltd – LICENCE NO. MI-2013-LI-03598-1 OF 6 Eastern Road, SOUTH MELBOURNE, VIC, 3205 – AT THE REQUEST OF THE MANUFACTURER.
Signed by
David Rowbury
Manufacturing Quality Branch
Delegate of the Secretary
2 July 2018