Monitoring the safety of medicines, which is also known as, pharmacovigilance, includes all activities related to the detection, assessment, understanding and prevention of adverse effects and other possible drug-related problems. This monitoring is carried out in a number of ways, including review and evaluation of suspected adverse reaction reports, published literature, epidemiological studies and additional clinical trial results. For helping your company on this, Klinar provides the services below:
Safety Management
● Assessment of drug/medical device adverse events
● Adverse event follow-up
● Adverse event classification
● Updating literature
● Literature follow-up
● Reporting to the authorities
● Building electronical tracking systems integrated with TUFAM (Turkish MoH) and periodically reporting
● Reporting to the company Adverse event notification
● Pharmacovigilance training (clinical drug studies) Pharmacovigilance training (accredited drugs) Serious Adverse Event Reporting
●Safety Notifications ( SUSAR Notification / IN Preparation and follow-up)
The Best Outsourcing Solution!
Full service CRO with Customer-Oriented project management and proposals
Excellent expertise with more than 350 completed projects.
High level of customer satisfaction with dedicated team work and synergy.
Clear strategies for your projects starting from the beginning.
Project and staff stability.
Quick start-up timelines with good communication to the ECs and RA.
Flexible, proactive, professional teamwork.
Competitive costs, Efficient processes
Open communication to our clients and employees
Good risk mitigation processes and planned business continuinity
Quality Certificates such as MoH GCP Certificate, ISO:27001 Information Security Management.
Micromanagement on project and site performence.
High patient recruitment level and efficient patient retention policies.
Recruitment strategies for targeted populations.