🔥 Find me at MedicalDevicesGroup.net 🔥
2 min reading time
Ooh, I’ve got a good one for you today: An FDA regulator is giving a special 90-minute webinar for Greenlight Guru and the Medical Devices Group. Shout out to Jon Speer for arranging.
Your free registration at https://medgroup.biz/case-quality.
Francisco Vicenty is the FDA Case for Quality Program Manager. You may be familiar with his work.
FDA launched the “Case for Quality” (CfQ) in 2011 after reviewing device quality data and feedback from FDA and industry. They flagged widespread manufacturing risks that impact product quality.
The presentation will emphasize the areas of focus that, when properly executed, give you fantastic benefits: Higher productivity, fewer complaints, fewer CAPAs and investigations, and lower quality-related product costs than your competitors.
You’ll be able to ask FDA questions – anonymously, if you like – during the call. So, while you can get the replay later, this might be a good one to attend live, Wednesday, July 11, starting at 11:45 a.m. New York time.
P.S. We only have 500 seats so register now at https://medgroup.biz/case-quality and forward this announcement to your colleagues.
𝗖𝗛𝗔𝗡𝗚𝗘 𝗢𝗙 𝗣𝗟𝗔𝗡𝗦
When: October 10-12, 2018
𝗢𝗨𝗥 𝗞𝗘𝗬𝗡𝗢𝗧𝗘 𝗦𝗣𝗘𝗔𝗞𝗘𝗥: Lance Black MD, the Med Device Innovation Lead at Texas Medical Center, the world’s largest med center on:
Locals, come at least for the keynote and reception.
• Prices 🔼 after July 4; full refund thru 8/16
Make it a great week.
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