The Department of Product Evaluation & Registration at BoMRA will conduct virtual
stakeholder sessions to discuss the medical devices including in vitro diagnostics (IVDs)
processes and guidelines: registration, risk classification, labelling, clinical evaluation,
registration timelines and fees. The stakeholder engagement targets all relevant
stakeholders inclusive of; manufacturers, importers, distributors, local representatives,
associations and facilities.

The sessions will be scheduled as follows:

SESSION 1: Tuesday 18th October 2022 from 0830 – 1300 hours
SESSION 2: Wednesday 19th October 2022 from 0830 – 1300 hours

Please use the link provided below to register for the stakeholder engagement, kindly
complete the details on the relevant sessions for planning purposes. Additionally, detailed
information regarding each stakeholder engagement session will be communicated
directly to the confirmed attendees. The following stakeholders should register for the
sessions below respectively. Please register before October 10, 2022.

SESSION 1: Local stakeholders
Link: https://forms.gle/EZ3Re2QPqjM5FFbK6

SESSION 2: International stakeholders
Link: https://docs.google.com/forms/d/e/1FAIpQLScxkcgenILcwmhCRyi7lAfrjIKH0ETcCSomTkwV-at6jI7NQ/viewform?usp=sf_link