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Our Perioperative Care Framework

Our Perioperative Care Framework maps the patient’s journey from the time surgery is contemplated through to an optimal outcome.

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Environmental Sustainability Network

The purpose of the ESN is “to advocate, collaborate and promote initiatives and projects related to environmental sustainability within anaesthesia, perioperative and pain medicine”.

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Product defect correction: Carestation 750/750c Anesthesia Delivery Systems – O2 mixer failure condi

Defect in these machines causes defaulting to 100% O2 ventilation, risking hyperoxia and oxygen toxicity if ventilation is prolonged for some patients.

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Jannsen-Cilag CADD Infusions Systems Disposables product defect

Jannsen-Cilag CADD Infusion Systems Disposables as part of Veletri Consumables Kit may underdeliver infusion doses or fail to detect attachment of the cassettes.

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Primary exam preparation courses (formerly Part 1)

We offer a range of activities around Australia and New Zealand specially designed to help trainees prepare for the written and oral components of the ANZCA primary exams. Find out what's available in your area.

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ANZCA National Anaesthesia Day

Each year we celebrate ANZCA National Anaesthesia Day across Australia and New Zealand on 16 October, the anniversary of the day in 1846 that ether anaesthetic was first demonstrated in Boston, Massachusetts.

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BJA personal subscriptions

As a member, you can subscribe to the high-impact British Journal of Anaesthesia (BJA) at a heavily discounted personal subscription rate.

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Skantha Vallipuram ANZCA research scholarship

The future of research depends on helping emerging investigators transition to established researchers

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Misaligned volume markings on BD 5mL syringe

Graduated volume markings are reported to be misaligned on the BD (Becton Dickinson) 5mL luer-slip syringe, item number 302130, leading to measurement error.

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Product defect correction: damaged barrels on BD Plastipak 50mL Syringe with Luer-Lok Tip

Damaged barrels may admit air. Check all devices before, during and after use, and report any defective devices discovered.

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