WHAT | WHY | HOW | WHO
Find out all you need to know in our combined SEMINAR & WORKSHOP
Are you ready for change?
The In Vitro Diagnostic Regulation (IVDR) entered into force in 2017 and will apply from May 26th 2022. Since this is a regulation and not a directive it will be part of the local regulation in all member states. Transitioning to IVDR will be challenging. If you have not initiated work yet, or are still in the early stages, we can help you to take a major step forward.
At PlantVision we have extensive experience working with all areas of regulatory compliance. We offer a range of flexible IVDR support services including workshops, seminars, gap analysis, transition planning, continuous support and training.
Combined SEMINAR & WORKSHOP
Get things moving in the right direction with a free TWO HOUR seminar & workshop together with our IVDR specialists.
We will come to your company and introduce you and your colleagues to the challenges and changes ahead. During the workshop part of the activity we will help you to identify the specific challenges your organization faces as it transitions to IVDR.
What you will learn
- An introduction to In Vitro Diagnostic Regulation
- Similarities and differences between IVDD and IVDR
- The main changes ahead, including what you need to cover in your technical documentation
- How to prepare for the implementation date in 2022
- Identifying the main challenges that your company is facing
Book your Seminar & Workshop today!
Product Manager Compliance Excellence
Please send me an email with your contact information (name, job title, company, tel nr.) and someone from our IVDR team will get in touch to arrange a time and a place for your seminar & workshop.
It is helpful if you can also provide some brief background information about your company and current situation.
I look forward to hearing from you!