REDI Initiative Engages SeerPharma for Workforce Skills Gap Training

The Researcher Exchange and Development within Industry (REDI) program is funded by the Australian Government’s Medical Research Future Fund and operated by MTPConnect. REDI has undertaken a comprehensive analysis of skills gaps in the Medical Technology, Biotechnology and Pharmaceutical (MTP) sector and identified several critical skills gaps that inhibit the industry maximising the impact on healthcare in Australia.

The REDI training below contributes to closing the skills gaps by addressing Quality Management Systems (QMS) for the MTP sector. 

REDI QMS Training Program Structure (1200x459)

Specifically, the REDI training includes a FREE wholly online (eLearning) QMS Primer that provides foundational knowledge and then 3 deep-dive, instructor-led workshops on specific QMS Standards. The QMS Primer is optional, participants with a basic QMS understanding and that know which QMS Standard their operations are best-aligned to can directly register for a workshop.


Introductory online training on quality management system definition, history and evolution and then specific applications through ISO 9001, ISO 13485, ISO 17025 and Good Laboratory Practice (GLP) Standards as well as Corrective Action and Preventive Action (CAPA) being the 'heart' of QMS.

QMS Primer Information

ISO 9001 Quality Management System - Requirements

Deep-dive workshop training on ISO 9001: a QMS standard for any size organisation in any industry and helps the business focus on quality, consistency, continuous improvement and customer satisfaction.

ISO 9001 Workshop Info. (fees & schedule)

ISO 13485 QMS for Medical Devices

Deep-dive workshop training on ISO 13485:  which is based on ISO 9001, but adapted specifically for the medical device supply chain.

ISO 13485 Workshop Info. (fees & schedule)

Good Laboratory Practice (GLP)

Deep-dive workshop training on Good Laboratory Practice (GLP): a managerial quality control system covering the organisational process and the conditions under which non-clinical health, safety and environmental studies are planned, performed, monitored, recorded, reported and retained (or archived).

GLP Workshop Info. (fees & schedule)

If you have any questions, please contact us to discuss your interest and how we can help.

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