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RA Watch 8 – Experiences with 2021 changes to MD regulatory framework

June 2023
June 2023 Experiences with 2021 changes to MD regulatory framework
Navigating the 2021 changes to the medical device regulatory framework

Editorial | Navigating the 2021 changes to the MD regulatory framework
June 2023 Experiences with 2021 changes to MD regulatory framework
Regulatory developments in the medical devices sector: A long and difficult journey

Deep Dive | MD regulatory changes: A long and difficult journey
June 2023 Experiences with 2021 changes to MD regulatory framework
Changes to the medical device regulatory framework: Looking back – and forward

Feedback From | swissethics: Past and planned responses to MD regulatory changes
June 2023 Experiences with 2021 changes to MD regulatory framework
Swissmedic’s experience with the regulatory changes for clinical investigations with medical devices implemented in 2021

Feedback From | Swissmedic: A stakeholder-oriented response to MD regulatory changes
June 2023 Experiences with 2021 changes to MD regulatory framework
Challenges facing Switzerland’s medical technology industry following the 2021 changes to medical device legislation

Views and Opinions | Swiss Medtech: Challenges facing Swiss medtech industry
June 2023 Experiences with 2021 changes to MD regulatory framework
Patient input into medical device development: A missed opportunity

Patient advocacy | Patient input into MD development: A missed opportunity
June 2023 Experiences with 2021 changes to MD regulatory framework
The PES-SLEEP project: A practical approach to the categorisation challenge for studies with medical devices

Case Study | PES-SLEEP project: One approach to the study categorisation challenge

Download

You can download a PDF of this entire issue of Regulatory Affairs Watch.
RA Watch 8 – Experiences with 2021 changes to MD regulatory framework (pdf, 2.61 MB)