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BioWorld - Saturday, April 17, 2021
Home » Topics » Asia-Pacific » Australia

Australia
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Aussie device makers urge TGA to follow IMDRF lead on software regulations

Nov. 13, 2019
By Mark McCarty
No Comments
Australia's Therapeutic Goods Administration (TGA) recently posted a draft guidance for regulation of software as a medical device, but the Medical Technology Association of Australia expressed a preference for an international standard for risk classification.
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Australian-EU-flags

TGA asked to hold off on device reclassification pending implementation of EU's MDR

Nov. 13, 2019
By Tamra Sami
No Comments
Device makers were generally supportive of the Australian Therapeutic Goods Administration (TGA) proposal to up-classify active medical devices with an integrated diagnostic function that significantly determines patient management by the device (such as closed loop systems or automated external defibrillators) to class III, the highest risk designation used by TGA.
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Australian flag marking country on globe
AusBiotech 201

National stem cell roadmap provides cohesive vision, funding for Australia's regenerative medicine sector

Nov. 12, 2019
By Tamra Sami
No Comments
MELBOURNE, Australia – Although Australia was one of the first movers in the regenerative medicine space, until now a cohesive plan for investing in regenerative medicine was holding the sector back.
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Globe showing Australia

Australia moves to reclassify implantable spinal devices to mirror EU device regulations

Nov. 8, 2019
By Tamra Sami
No Comments
PERTH, Australia – Although medical device industry stakeholders agreed in principle with the Australian Therapeutic Goods Administration's (TGA) proposal to align its classification with the EU's for implantable spinal devices, they viewed the interpretation of the EU Medical Device Regulation (MDR) classification rule for these devices differently.
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Globe showing Australia
AusBiotech 2019

Australia's biotechs grapple with reimbursement system for cell therapies

Nov. 6, 2019
By Tamra Sami
No Comments
Although Australia's Therapeutic Goods Administration (TGA) approved its first CAR T therapy in 2018, the country is lacking a system to reimburse those advanced therapies, and industry is calling on government to revalue gene therapies.
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Genetic-Signature-product-line

Genetic Signatures ready to go global with AU$35M raise

Nov. 6, 2019
By Tamra Sami
No Comments
PERTH, Australia – Sydney-based molecular diagnostics company Genetic Signatures Ltd. is poised to extend its global footprint to the U.S. and Europe following its AU$35 million (US$24 million) capital raise.
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Virocure's Australian branch launches operations with an oncolytic virus phase I trial

Oct. 30, 2019
By Jihyun Kim
No Comments
HONG KONG – South Korean biopharma Virocure Inc., based in Seoul, recently founded a local corporation in Brisbane, Australia. The new company, Virocure Australia Pty Ltd., will facilitate a phase I trial of the experimental cancer drug RC-402 in Australia.
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From mold to therapeutic gold?

Promising new analgesics developed from Australian mold

Oct. 30, 2019
By John Fox
No Comments
Australian scientists have discovered promising new candidate analgesic molecules derived from a Penicillium fungus, which represents a promising resource for the development of safer new analgesics, they reported in the Oct. 14, 2019, edition of Proceedings of the National Academy of Sciences.
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From mold to therapeutic gold?

Promising new analgesics developed from Australian mold

Oct. 24, 2019
By John Fox
No Comments
Australian scientists have discovered promising new candidate analgesic molecules derived from a Penicillium fungus, which represents a promising resource for the development of safer new analgesics, they reported in the Oct. 14, 2019, edition of Proceedings of the National Academy of Sciences (PNAS).
Read More

Australia’s Orthocell ready to file on interim Celgro data

Oct. 16, 2019
By Tamra Sami
No Comments
PERTH, Australia – Following stunning interim clinical results for its Celgro nerve regeneration treatment in quadriplegic patients, regenerative medicine company Orthocell Ltd. will focus all its efforts on gaining early FDA approval based on the early results.
Read More
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