Webb24 aug. 2024 · TGA is investigating the presence of an azide impurity in sartan medicines. As has happened in other countries, the discovery of low levels of the contaminant in batches of losartan and irbesartan drug products has triggered recalls in Australia. Webb21 mars 2012 · * COMPLAINTS AND RECALL OF PHARMACEUTICAL AS PER THERAPEUTIC GOODS ADMINISTRATION (TGA) 1.1.1 Objective: Objective of the guidelines under this element is that a defective product is immediately recalled ,matter is investigated & remedial measures are taken. All verbal or written complaints or reports …
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Webb15 juni 2024 · authorisation holder for the issues identified • Maintains product distribution details (and provides to the TGA) to assist in. facilitating a recall action • Has … WebbA recall/non-recall submission is used to notify the TGA of issues in relation to therapeutic goods supplied to the Australian market. This form may also be used to notify TGA of … prenanthes sagittata
Revision of the Uniform Recall Procedure for Therapeutic ... · …
WebbTGA Recall Reference: RC-2024-RN-02255-1: Product Name/Description: Proshield N95 Small Surgical Respirator Batch number: 04NOV20 Expiry date: 04/11/2025 ARTG … Webb17 nov. 2024 · The Therapeutic Goods Administration (TGA), an Australian regulating authority in the sphere of healthcare products, has published a guidance document … WebbURGENT MEDICINE RECALL TGA Ref Number: RC-2024-RN-01478-1 TENOFOVIR DISOPROXIL EMTRICITABINE MYLAN 300/200 Aust R 265834 tenofovir disoproxil … scott bolden wife