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Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Dec. 7, 2016

View Archived Issues

Australian firms hope for even faster approvals under proposed legislation

PERTH, Australia – Drug and device companies in Australia may soon be able to bring their products to market more quickly via a new priority review designation. Health Minister Susan Ley introduced legislation to Parliament on Dec. 1 that would speed the approval of drugs and devices by providing Australia's Therapeutic Goods Administration (TGA) with new priority review mechanisms. Read More

Supreme Court, PTO lined up to hear life science patent cases

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Clotchip aims for real-time identification of bleeding risk

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Getting out of the balkanized biomarker bargain basement

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Blood substitute passes first acid test

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Financings

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Product briefs

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Appointments and advancements

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Other news to note

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MDD's Oncology Extra

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