MEMORANDUM
The CDRRHR shall be holding the aforementioned activity on 19 September 2019,Thursday, 9:OOAM – 12:OOPM at the FDA Lobby.
The Kapihan at Talakayan aims to provide a venue for the discussion, clarification and/or suggestion on the implementation of Administrative Order No. 2018-002, Guidelines Governing the Issuance of an Authorization for a Medical Device based on the ASEAN Harmonized Technical Requirements.
All interested parties may signify their attendance thru registration by e-mail at [email protected]. Registration shall be on a first-come, first-serve base and one (I) representative shall be allowed per company.
A total of 100 slots shall be made available and confirmation as an attendee shall be made via e-mail.
For your information and guidance.
Attachment-> : KAPIHAN AT TALAKAYAN SA FDA FOR MEDICAL DEVICE ESTABLISHMENTS