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Oct 20 New EU Regulation OCRA

Orange County Regulatory Affairs Discussion Group (OCRA) is inviting QA/RA management as well as key decision makers (CEO, CFO, and Internal Counsel) to discuss the business and financial implications of meeting the new regulations and engage with both seasoned Industry and Notified Body professionals to obtain valuable insights and information on how to proactively prepare for the transition to the new EU regulations for medical devices and IVDs.5.

This year, Jawad Mahdavi, Lead Auditor at LNE/G-MED North America will discuss the new MD regulation and its Implications for Medical Device manufacturers.

To download the program and register, click here.


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MDSAP Prepare the transition, worldwide market access

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Due to our rapid growth in North America, we're seeking Lead Auditors.