DMTC Limited has engaged Australian indigenous-owned small business Willyama to undertake a comprehensive cyber security audit of systems to be deployed through DMTC’s Industry Capability Development Program.
Willyama’s team of security analysts will review DMTC’s Smart Enough Factory solution which seeks to realise benefits of Industry 4.0 adoption for Australian small businesses, and to equip those companies to contribute to defence sector supply chains. (more…)
DMTC is working with Australia’s dedicated submarine sustainment organisation, ASC, and the CSIRO to pioneer the use of additive manufacturing for the repair of Collins Class submarines. (more…)
As part of its contribution to the national COVID-19 response, DMTC has teamed with the Advanced Manufacturing Growth Centre to produce a video highlighting four simple steps that manufacturers and Aussie defence companies can take in returning to the workplace.
Resilient supply chain partners can work together to get the job done, in line with the Government’s safe work principles.
A clinical trial has commenced to test the effectiveness of a low-dose regimen of the anti-malarial drug Chloroquine to prevent coronavirus illness.
The clinical trial is being funded by Defence and managed by the national Medical Countermeasures Initiative led by DMTC Limited. Experts with experience in clinical trials from DMTC are working alongside personnel at the trial site, the ADF Malaria and Infectious Diseases Institute.
The trial will focus on military healthcare and civilian healthcare workers at the frontline of the national response to COVID-19.
Chloroquine is a well-known drug that is already used around the world for the prevention and treatment of malaria as well as the treatment of some inflammatory and connective tissue diseases.
DMTC CEO Dr Mark Hodge urged caution in the race to provide answers to combating COVID-19.
“Clinical trials are essential to establish global benchmarks and ultimately to prove whether this drug, at these prescribed dose amounts, can prevent infection,” Dr Hodge said.
“Novel medications can take a long time to get through all the tests and approvals that are needed to confirm safety, quality and effectiveness. Re-purposing of an existing drug with a known safety profile has potential benefits in regard to expediting conclusive results.”
Because its safety profile is well understood, the trial can be undertaken rapidly to the high standards required by Australian and international pharmaceutical regulators. (more…)
