The Center for Device Regulation, Radiation Health and Research will be conducting a dialogue with the medical device industry regarding the compliance of the new regulatory guideline for medical device registration.
This is a two session-activity on December 15 and 16, 2015 from 8am to 5pm the venue will be announced later. The same topic will be discuss on both days.
Each company will choose which day they will attend.
They could confirm their preferred date either through your organization or directly to us. They need to submit their name, designation, company, telephone no. And email address. Deadline of confirmation is on December 3, 2015. Allotted seat per day is only for 60pax.
This is an advocacy activity in line with the implementation of AMDD.
Thank you so much and looking forward to your participation in this activity.
Very truly yours,
Ma. Cecilia C. Matienzo