Regulatory Resources
This phrase—delivered by one of Health Canada | Santé Canada’s senior regulators during Medtech Canada’s annual regulatory and quality conference in Ottawa last week—captured the tone...
Medical Devices Regulatory Raconteur
The Regulatory Rapporteur 2025 first edition starts with changes at home, an exhaustive update on the Canadian Medical Devices Regulations SOR/98-282.
Medical Devices Regulatory Raconteur
I am once more struck by the relaxed atmosphere, the partnership between industry and regulators and shared interest to address the needs of a small market while considering global implications.
Medical Devices Regulatory Raconteur
Check out Hasnaa's conversation with the Editor of The MedTech Strategist on how to add value as a Regulatory team player.
Medical Devices
Read our latest article on Canadian Regulations, recently published in the TOPRA peer-reviewed journal Regulatory Rapporteur.
Medical Devices
I recently read an article on increasing Diversity in the Regulatory Affairs Profession. I was quite excited at first, and even more so when I saw a section dedicated to utilizing “new immigrant” talent for diversity purposes, only to find in cliché statements such as multilingualism and knowledge
Medical Devices
In a recent LinkedIn post, I spoke about Health Canada’s plan to make the REP (Regulatory Enrolment Process) mandatory 18 months after its projected implementation date (January 2024). In another post, I summarized the list of proposed amendments to the Canadian Medical Device Regulation, for which
Medical Devices
Even though Taiwan’s health tech has prevented the pandemic, MedTech regulations specialist Hasnaa points out that establishing a closer connection with the global south is the key to make Taiwan a leader in innovation of health tech.
Medical Devices