The Department of Product Evaluation & Registration (Medical Devices Unit) at BoMRA
cordially invites all stakeholders to a consultative engagement meeting. Discussions will
include among others:

• Legislative and regulatory requirements updates
• Medical devices registration roadmap
• Regulation enforcement and compliance updates
• Any other relevant regulatory matters

Target Audience: the engagement targets the following stakeholders dealing with
medical devices including IVDs:

• Healthcare facilities (hospitals, clinics, medical laboratories, etc.), healthcare
professional associations, retailers, importers (logistics companies) and import control,
manufacturers, distributors, wholesalers, and local authorized representatives