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Post Market Surveillance
(PMS) Services 

Artixio’s Post Market Surveillance (PMS) services are designed to ensure the ongoing safety and efficacy of medical products after they have entered the market. These services include continuous monitoring of product performance, collecting and analyzing adverse event data, and ensuring compliance with global regulatory requirements. Artixio’s team of experts conducts thorough risk assessments, prepares detailed PMS reports, and provides actionable insights to mitigate potential risks. By leveraging advanced data analytics and maintaining close communication with regulatory authorities, Artixio helps clients maintain high safety standards and regulatory compliance, ultimately safeguarding public health.

Intake Services

Receive AE/PQC/MI via calls/fax/email/website/affiliates
Complaint documentation
Mailbox management
Social media screening

Product Complaint Management

Handling of product complaints for Pharma/Medical devices
Defective sample handling
Coordination for Investigation Report

AE Case Processing

AE Intake & Triage
Case processing in safety database
Narrative writing
Medical Review
Submission
Follow up

Literature Management

Literature screening of global & local literature
Design search strategy
Validity assessment of literatures
Review of ICSR & Non-ICSR
Full text article procurement
Translation
post marketing surveillance medical devices pharmaceuticals adverse event reporting case processing

Get in touch

Our experts will be delighted to assist you with your global business needs.

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