What will the webinar cover?
The COVID-19 pandemic has forced the medical device and IVD sector to consider new and innovative ways of meeting regulatory demands while keeping patient safety at the forefront of our role. As a sector, we have risen to the challenge of COVID-19 with professionalism and resilience, and we have found new ways of ensuring we meet our responsibilities.
Join us for our Medical Devices webinar on hybrid audits – the new way of working post pandemic. We will share our audit lessons learnt during the pandemic as well as how best to plan for future audits. We will also focus on unannounced audits and maintaining regulatory compliance, whilst also focussing on our sustainability commitment.
Who should attend the webinar?
The webinar is open to everyone in the medical device industry, including manufacturers, quality managers and consultants.
What will participants gain?
Join this valuable webinar to hear from Linda Moon, Global Quality & Accreditation Manager, Regulatory Services, as she talks about why we are using hybrid audits and how they can help improve better client service levels. Linda will also be joined by subject matter expert Dr. Yoann Buisson, GQA Technical Manager, Regulatory Services.
The webinar will include:
- An understanding of BSI Regulatory Services plans for hybrid auditing
- An introduction of what to expect at a hybrid unannounced audit
- Lessons learnt from our experiences of hybrid audits
- Why we are moving to a hybrid audit programme
- What the difference in the experience will be for you
- Effectiveness of hybrid audits
- Sustainability benefits
- Geographical constraints
- Investment in technology
