SeerPharma are strategic partners with market leading software solution provider – MasterControl. Our partnership, over the last 7 years, has seen us deploy this solution to digitise Quality and Manufacturing workflows to over 75 companies.
MasterControl is running a webinar on current industry trends facing Quality and Manufacturing professionals in the Medical Device industry. Hear from MasterControl’s Senior Vice President of Go to Market Strategy – Martin Smyth, and Senior Product Marketing Manager – Jessica Madsen, as they provide insights from MasterControl’s global reach across the Medical Device landscape.
The webinar will address regulatory, technology, economic, and therapeutic trends in the sector. These include a continued focus on cybersecurity as part of medical device quality management, challenges with artificial intelligence (AI) in medical devices and software as a medical device (SaMD), and how to improve medical device manufacturing in a tighter investment environment. Familiarising yourself with these 2024 trends and how to take advantage of them can make all the difference in the competitive medical device market.
Key takeaways will include:
- Medical device industry trends you need to know to stay competitive
- How technology is affecting medical device quality and manufacturing
- How medical device compliance will change in light of new regulations
The free webinar will be held on Wednesday the 21st of February at:
- 10:00am Perth & Singapore
- 12:00pm Brisbane
- 12:30pm Adelaide
- 1:00pm Melbourne & Sydney
- 3:00pm Auckland
Click the link below to visit MasterControl's event webpage when you can learn more about the presenters and register your attendance via the "Register Now" button at the top.
2024 Medical Device Trends for Quality and Manufacturing - Webinar (mastercontrol.com)
If you'd like to learn more about how SeerPharma supports the medical device sector with Consulting, Training, MasterControl software, and Contracting solutions that support compliance with ISO 13485:2016 Standard or FDA 21 CFR Patt 820 (medical device quality management system requirements) amongst other regulations and standards, please click here.
