DEFI has the faculties to carry out activities as assistant in he Health Inspection for:
Drugs:
Creation of the Sanitary Registration approval for Allopathic Drugs.
Administrative modifications to the conditions of the Sanitary Registration of Allopathic Drugs, Vitamins and Dietary and Herbal supplements.
Technical modifications to the conditions of the Sanitary Registration of Allopathic Drugs, Vitamins and Dietary and Herbal supplements under the terms of articles 185 and 186 of the Health Supply Ruling.
Sanitary registration renewals for Allopathic Drugs, Vitamins and Dietary and Herbal supplements.
In the area of medical devices.
Certified for reviewing:
Sanitary Registration of Class I, II and III Medical Devices, under the terms of articles 179, 180 and 181 of the Health Supply Ruling.
Modifications to the conditions of the Sanitary Registration (Administrative and Technical) of Class I, II and III Medical Devices under the terms of article 184 of the of the Health Supply Ruling.
New Certification
We are proud to start 2016 with DELFILATINA newly certified as a licensed third party to review registration, modifications and renewals of biotechnological drugs as well as allopathic drugs, Vitamins, dietary and herbal supplements and medical devices.
Registration, renewal and modification for synthetic allopathic drugs IV,V,and VI.
Registration, renewal and modification for biotechnological drugs
Registration, renewal and modification for medical devices I, II, III except those that count with equivalent agreements.
Registration, renewal and modification for herbal and vitamin medications.
WE ISSUE
We issue veredicts regarding the compliance of requirements established by the Ministry of Health in the corresponding legal Norms so we can guarantee sanitary authorization.
WE ISSUE
We issue Technical reports recognized by Cofepris for authority acts.
WE EVALUATE
We evaluate compliance based on standardized procedures and a quality system.