Lab business > Regulations

Report released into Qld's "flawed" DNA extraction method

21 November, 2023 by Lauren Davis

The 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, 2023

The 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 Davis

Emergency 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 Davis

Emergency 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, 2022

Manufacturers 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, 2022

An 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, 2022

Vaisala 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 Integrity

The 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 Staff

Compliance 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, 2021

Good 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, 2021

Australians 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, 2020

The 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, 2019

Australian 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.


New DNA data protection laws needed, say researchers

20 December, 2018

New laws are required to control access to medical genetic data by law enforcement agencies, according to researchers at the University of Queensland.


An education in ethics

16 August, 2018 by Lauren Davis

Bioethicist Dr Ainsley Newson talks mitochondrial donation, targeted testing and other ethical dilemmas ahead of the AACB AIMS 2018 Combined Scientific Meeting.


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