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Archives for April 2019

Post-Market Data: What You Need to Know

A lot of companies do risk management ONLY when making changes to a product. That’s going to change, says Principal Consultant at Gish Consulting, Christine Zomorodian. Regulators are looking at new requirements for risk-based clinical evidence of performance and safety for both new and existing products.

Anne Leijsen, Head of Medical Writing at Factory CRO, takes you through the new product development lifecycle — the interaction between risk management, clinical evaluation and post-market surveillance. She shows you how to collect post-market data and what to DO with it.

Post-Market Data: What You Need to Knows
Presented by Christine Zomorodian and Anne Leijsen
at 10x for Design and Manufacturing – San Diego 2018


Click for the slides and transcript. »