Webinar on demand desktop-monitor.png

After-market Aftermath Webinar Series - Part 1: The Aim of Post-Market Surveillance

Post-Market Surveillance (PMS) is a crucial step for manufacturers in the pharmaceutical and medical fields. Collecting data and reporting its analysis is part of quality & regulatory compliance and helps monitor the performance of commercialized products available on the market.

Have 30 minutes to spare? Join expert Seyed Khorashahi as he covers the difference between PMS and vigilance, the methods and processes used to monitor product performance and the overall PMS requirements.

Watch now for free



Seyed Khorashahi has more than 25 years’ experience leading teams in all aspects of developing safety critical medical devices. He has held leadership positions at Covidien (Medtronic), Baxter, and Beckman Coulter, Inc. prior to joining RCA 5 years ago, and has an extensive background in medical device product development, quality systems, regulatory affairs, and mergers and acquisitions. Other core competencies include engineering and business strategy.

Seyed has significant domain expertise not only in FDA and EU standards, but also in software systems and hardware development for medical devices. He has a proven track record of efficiently deploying total product life cycle process improvements with extensive knowledge of 21 CFR 820 and ISO 13485 for management of medical devices throughout the medical device life cycle from product inception to product retirement