7 – Clinical Use, Vigilance, Surveillance & PMCF2018-03-14T15:41:08+00:00

Vigilance & PMS

GPB provide assistance to develop, implement and complete compliant, efficient Post Market Surveillance plans including the definition, recording and implementation of your controls.

PMS

This assistance can involve:

  • Consumer / Customer Feedback

  • Complaint Handling and Responses

  • Trend Analysis

  • Post Market Clinical Follow Up (PMCF)

  • Adverse Event / Incidents Management

  • Medical Device Reporting to relevant authorities

  • Field Safety Notice (FSN)

  • Field Safety Corrective Action (FSCA)

  • Corrective & Preventative Action (CAPA)

  • Standard Operating Procedures
  • Regulations & Standards
  • PMS Planning
  • Post Market Clinical Follow Up (PMCF)
  • Corrective & Preventative Action (CAPA)
  • Consumer and Customer Feedback
  • Complaints
  • Adverse Events
  • Device Returns
  • Reporting to Relevant Authorities:
  • Adverse Trends
  • Field Safety Notice (FSN)
  • Field Safety Corrective Action (FSCA)

Would you like to know more?

We are here to help  you with any enquiries you may have, if you would like to speak to a member of staff, please fill out the following contact form or feel free to contact us on one of the following: