Your questions, answered by people deep in the world of MedTech. Real, authentic, and driven by industry.
Why we started this
MedTech Open Office started as a simple idea between Adam and Monir — two people who kept seeing the same questions go unanswered across the industry. Professionals stuck on regulatory pathways, founders unsure how to navigate compliance, career changers with nowhere to turn. Rather than watch that continue, they decided to open the door.
The format is deliberately straightforward: a fortnightly live stream where anyone can submit a question and get a real answer from people who work in the industry every day. No gatekeeping, no PR polish — just honest, practical knowledge shared openly.
Live Q&A format
Submit questions ahead of time or drop them in the stream chat on the day.
Industry insider knowledge
Two hosts with hands-on experience across regulatory, quality, strategy, and commercial MedTech.
Every two weeks
Consistent, accessible, and free — live every two weeks.
Community
Join the WhatsApp community to stay connected between episodes and keep the conversation going.
Episode schedule
Every two weeks, 6–7 PM Central European time. Times below are shown in Central Europe, the UK and US Eastern, and adjust automatically when the clocks change.
The first date is being set
Episodes will run every two weeks, 6–7 PM Central European time. The schedule fills in here as soon as the first date is fixed — and the community hears about it before the website does.
Join the WhatsApp communityThe people behind the mic
Monir is a MedTech entrepreneur and regulatory strategist with deep roots in the European medical device ecosystem. As founder and CEO of Easy Medical Device, he leads a consultancy helping manufacturers achieve compliance across EU MDR, IVDR, FDA, and global markets. He works at the intersection of regulatory affairs, quality systems, market access, and digital health — and has built one of the most accessible MedTech education platforms in the industry through podcasts, magazines, and live content.
→ easymedicaldevice.com
Adam is a Chartered Quality and Regulatory Professional and founder of The Other Consultants, a Glasgow-based MedTech consultancy. With nearly a decade of independent consulting experience, he holds dual roles as a Lead Certification Auditor across ISO 13485, UK MDR, EU MDR, MDSAP, and QMSR schemes. Having worked across organisations including Thermo Fisher Scientific, Siemens, and Stryker before moving into consultancy, Adam brings a uniquely dual perspective — he understands auditing, and he understands being audited. He covers device classes I through IIb across global markets.
→ theotherconsultants.comPrevious episodes
Every episode is recorded, so missing one live is never a problem.
The first episode is on its way
Once the show is running, every episode will appear here to watch back. Join the WhatsApp community and you’ll know the moment the first one is live.
Submit your question
How it works
Send your question before the show and we’ll do our best to cover it live. The more context you give, the better the answer.
Can’t make it live? Every episode is recorded and available to watch back shortly afterwards.