The STEMM Central Bootcamp is a program jointly administered by the Cancer Therapeutics CRC and Biomedical Research Victoria.
The STEMM Central Bootcamp is a series of modules providing Medical Researchers with a foundation in the research translation and commercialisation process. This includes skills such as market and competitor analysis, intellectual property management and regulatory intelligence as well as design thinking, negotiation and relationship building. Ideally designed to be completed as a whole, the program consists of individual modules. Each module consists of a masterclass presented by area experts, supported by webinars and print resources to further deepen understanding of the topic.
SeerPharma was invited to run the final masterclass, on regulatory issues. In this module, the participants were introduced to the regulatory framework and regulatory bodies, the approval processes for medicines and medical devices and the timelines of application guidelines involved.
The class was well received, and, in addition to the Postgraduate course on Good Manufacturing Practice (GMP) that we run at the University of Technology Sydney, is further testament to our commitment to assisting the next generation of professionals entering the pharmaceutical and medical device industries.
Contact us if you’d like more information on mentoring new staff on the intricacies of working within a regulated environment.
This post comes from our July 2017 Journal. You may also be interested in:
- GMP Data Integrity Masterclass
- Assistance with New Medical Device Regulation (MDR) in Europe
- Navigating the Pathway of TGA Enforcement of the PIC/S Guide to GMP
