The International Medical Device Regulators Forum (IMDRF) recently updated its procedures for membership and for developing and managing technical guidelines.
The 40-page Standard Operating Procedures (SOP) document was prepared by the group’s Management Committee. The guide is intended as a complement to the IMDRF Terms of Reference (ToR) and describes the procedures for revising the membership of the IMDRF Management Committee, establishing subcommittees and working groups, and developing IMDRF documents or managing documents developed under the Global Harmonization Task Force on Medical Devices (GHTF)…
