The need for quality assurance in histopathology laboratories
01 October, 2024In histopathology laboratories, where tests are considered the gold standard for diagnosing various diseases, errors can significantly impact patient outcomes.
Avoid adverse regulatory action with comprehensive quality
01 October, 2024Attention to detail is par for the course within most modern industries and fields, including scientific research.
Report released into Qld's "flawed" DNA extraction method
21 November, 2023 by Lauren DavisThe report found that Project 13, which introduced automated DNA extraction methods to the Queensland Health forensics laboratory, was a "fatally flawed" project.
Second inquiry launched into Qld forensic testing
06 October, 2023The new inquiry will review recent public statements and documents in relation to automated DNA extraction methods that were introduced under what is known as Project 13.
Radioactive capsule found in Pilbara after week-long search
02 February, 2023 by Lauren DavisEmergency services have found a tiny radioactive capsule near Newman in Western Australia's Pilbara region, ending a large-scale interagency search for the missing object.
Radioactive capsule remains lost in Western Australia
31 January, 2023 by Lauren DavisEmergency services are searching for the capsule and are asking the public to report anything that looks like the missing material, which has been described as small, round and silver.
Best practices vital to navigating medical device post-market surveillance
02 December, 2022Manufacturers of medical devices must put in place a wide range of processes and documentation to meet post-market surveillance requirements.
Qld forensic scientists provided misleading information: report
26 September, 2022An inquiry into forensic DNA testing in Queensland has found there was potential for the miscarriage of justice.
Vaisala webinar on validation expertise in GxP environments
01 September, 2022Vaisala is running a webinar for anyone who has ever struggled with validating/qualifying GxP environments, providing attendees with the opportunity to get their questions on validation answered.
Are you ready for the TGA's GCP inspection program?
18 July, 2022 by Associate Professor Peter Keller, Senior Manager, Research IntegrityThe program shifts the chance of any one trial site being routinely inspected by the TGA from zero to about 4%, with the expectation that this will improve compliance.
Laboratory equipment's role in transitioning from research to GMP
01 September, 2021 by Life in the Lab StaffCompliance with GMP requirements plays a critical role in assuring patient safety by ensuring the production of consistently safe and effective products.
GMP warehouse mapping: step-by-step guidelines for validating life science storage facilities
01 June, 2021Good manufacturing practice (GMP) regulators have sharpened their focus on warehouse storage and distribution practices.
Have your say on reform of Australia's measurement laws
19 April, 2021Australians are invited to provide feedback on options proposed for modernising Australia's regulatory framework for measurement.
WHO advises against remdesivir use in COVID-19 patients
02 December, 2020The antiviral drug remdesivir is not recommended for patients admitted to hospital with COVID-19, regardless of how severely ill they are.
Maintaining standards in Australian labs
30 May, 2019Australian laboratories are subject to major audits every two to four years, with all necessary documentation checked to ensure that laboratories are meeting industry accredited standards.
