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Let’s continue our series on the life path of medical devices! 🔃 We’ve reached the 8th step, which focuses on PMS (Post-Market Surveillance) and PMCF (Post-Market Clinical Follow-up) activities.

Let's continue our series on the life path of medical devices! 🔃 We've reached the 8th step, which focuses on PMS (Post-Market Surveillance) and PMCF (Post-Market Clinical Follow-up) activities.

Here are the key objectives of PMS and PMCF 👇

📊 Real-world data collection ➡️ Essential for PMS and PMCF activities. PMS data includes sales, non-clinical complaints, and marketing information, while PMCF data involves clinical safety, side effects, and benefit/risk profiles.

📋 Data processing and feedback ➡️ All PMS and PMCF data must be proactively collected, regularly processed, and the results channeled back into risk management documentation, clinical evaluation processes and planning or development phases (if required).BiTrial supports your company throughout this process, helping ensure compliance and the successful implementation of PMS and PMCF activities. For more details, visit our website to explore our services. 🚀

About BiTrial

BiTrial Clinical Research combines the advantages of a regional CRO – cost-effectiveness, local knowledge, personalized service, and flexibility – with the expertise and understanding that comes from a history of managing global clinical trials at the highest standards of quality.