Monday, December 19, 2011

FDA Regsitration Renewal

written by : Beena, Regulatory specialist, LMG
Published on 12-19-2011

All medial device Establishments registered previously with FDA is required to complete the annual registration before Dec 31, failure to register your establishment by December 31, 2011 may result in your establishment being removed from FDA's database of active registrants.

Liberty Management Group LTD, the leading FDA consulting group providing assistance to medical device manufacturers with establishment registration, renewal, device listing, medical device label compliance etc... can help you with annual registration renewal

more information please visit http://www.fdahelp.us/medical_device_registration_renewal.html

Sunday, December 4, 2011

FDA LASIK

LASIK is a surgical procedure  to reduce a person's dependency on eye glasses or contact lenses. LASIK (Laser-Assisted In Situ Keratomileusis) commonly known as laser eye surgery is a procedure that permanently changes the shape of the cornea, the clear covering of the front of the eye, using an excimer laser.
To visit FDA-Approved Lasers for LASIK please click on the below url