Pharmacovigilance

Since 2015 LLP ConsultAsia has been providing a full range of Pharmacovigilance services in the Republic of Kazakhstan, namely:
— Continuous control of drug safety in the market of the Republic of Kazakhstan according to the order No. 421 of the Minister of Health and Social Development of the Republic of Kazakhstan “On approval of the Pharmacovigilance Rules for Medicines and Monitoring of Adverse Effects of Medicines, Medical Devices and Medical Equipment» dated May 29, 2015;
— Performing the functions of a qualified authorized person for Pharmacovigilance in the territory of the Republic of Kazakhstan;
— Advising on Pharmacovigilance System Master File;
— Preparation of Standard Operating Procedures;
— Preparation of periodic reports on the safety of medicines in accordance with the requirements of the Minister of Health of the Republic of Kazakhstan;
— Preparation of Risk Management Plans (RMP) as required by the Minister of Health of the Republic of Kazakhstan;
— Submission CIOMS to an authorized organization;
— Interaction with regulatory organizations, representatives of partner companies.