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Malfunction reports. The obligations of medical device manufacturers and distributors
Professional and efficient reports of malfunctioned medical devices is crucial to any organization. read more... -
THE IMPORTANCE OF REPORTING ADVERSE EVENTS RELATED TO DRUGS AND MEDICAL DEVICES
Reporting adverse events related to drugs and medical devices to the appopriate authorities can benefit public safety. Not all people react similarly to medicine, hence these reports will help documntation and better prevention of future adverse events. read more... -
An update to the procedure of reporting side effects and new safety information
In October of 2013 the Israeli Ministry of Health updated procedure 6 with the 3rd update read more... -
New service from Medicalix: Safety Alerts from 24 listed regulatory authorities
A new service Medicalix is offering to Pharmaceutical companies in Israel. This service will provide current updates of drug safety information published in 24 websites of regulatory authorities of recognized countries (EMA included). read more... -
Amendments & clarifications to procedure 6 updated 2
A clarification to procedure 6 that was published by the Ministry of Health on April 29th' 2013 read more... -
Dr Graeme Ladds, CEO and Operations Director at PharSafer UK- Pharmacovigilance
The 1st Israeli Pharmacovigilance Conference, 10 February 2013- Guest speaker read more... -
Just published: the draft for comments of MOH Israeli procedure for Adverse Event Reporting and New Safety Information
The Israeli Ministry of Health have published a draft for comments of the second update for the Procedure of Adverse Event reporting and New Safety Information. For a English translation of the draft guideline please see the below link.. read more... -
The 1st Israeli Pharmacovigilance Conference, 10 February 2013