@DeRam_David

CEO & Co-founder @greenlightguru, Helping #MedicalDevice Co's Bring Safer Products to Market Faster. | Founder of The http://t.co/kzog11s4mR

 Indianapolis, IN
greenlight.guru
Joined January 2015
  • Tweets2.6K
  • Following8.8K
  • Followers10.2K
890Media
The Ultimate Guide to Corrective and Preventive Action (CAPA) for Medical Devices Companies bit.ly/2A5ZfwN by @greenlightguru
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The Apple Watch is now a medical device. Greenlight Guru founder Jon Speer spoke with @chengela at The Verge about the difference between a device approval vs. clearance. bit.ly/2NISjiy

What the Apple Watch’s FDA clearance actually means

The FDA-cleared features aren’t supposed to be used by those under 22

theverge.com
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Free Webinar: Everything Device Makers Need to Know About Design Controls bit.ly/2FUThk0 hosted by @medicalmarcom & the 350k+ LinkedIn Medical Devices Group
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Greenlight Guru Launches New Software, Growing Team: ow.ly/BqyG30jSrsB #IIBTV @greenlightguru @TechPointInd @GerryDick
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Greenlight Guru Announces Multi-Level Design Control Software bit.ly/2HVDN51
Greenlight Guru is so proud to be a Best Places to Work in Indiana Winner!
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Free Webinar TODAY: What you need to know about the updates coming in the new EU MDR 2017/745 presented by @pathwiseinc & @greenlightguru bit.ly/2r12WzW
Why the FDA Presubmission Is an Underutilized Tool bit.ly/2HC1UFD by @greenlightguru via @qualitydigest
Only a few days left to register for our free webinar on "What you need to know about the updates coming in the new EU MDR 2017/745" in partnership by @pathwiseinc & @greenlightguru bit.ly/2HvuVmF
Only a few days left to register for our free webinar on "What you need to know about the updates coming in the new EU MDR 2017/745" in partnership with @pathwiseinc & @greenlightguru bit.ly/2HtAlOH
“However, if the leader can’t embody the company mission, it will fail. You cannot ask your team to do something you cannot do yourself.” Excellent point, @DeRam_David. A leader needs to buy in completely themselves before asking others to do so. entrepreneur.com/article/310…
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Free Webinar: What you need to know about the updates coming in the new EU MDR 2017/745 brought to you by @pathwiseinc & @greenlightguru bit.ly/2r1vTvD
A timeline to adopt medical device QMS (and why you need to act now) bit.ly/2HL8gBQ @greenlightguru via @medcitynew
Timeline to ISO 13485:2016 (And Why You Need to Act Today) bit.ly/2J1agmx
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Why I Only Hire People With 'Alligator Blood' | by @DeRam_David entm.ag/2yj

Why I Only Hire People With 'Alligator Blood'

I need employees who can go the distance and stay competitive when times get tough.

entrepreneur.com
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Greenlight Guru's Jon Speer shares what you need to know about FDA's new guidance on software as a medical device via @medcitynews bit.ly/2uwkRUj
Understanding the New Requirements for QMS Software Validation in ISO 13485:2016 bit.ly/2pwpGb4 by our partners @RookQuality

Understanding the New Requirements for QMS Software Validation in ISO 13485:2016

This blog post discusses the inclusion of new requirements for quality system software validation in ISO 13485:2016.

greenlight.guru
"If quality is just an afterthought, then you could be setting up a culture of ignoring or attempting to shortcut the rules." -Jon Speer. Check out his full interview with our partners @ResCol2141 here -> bit.ly/2IIXIRj
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Quality is the new black -- don't just focus on making the newest products, focus on making the best products. This and more of my insights @b2community bit.ly/2u7WtrD
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Will we see you at the Medical Device Technology Exchange (MDTX) April 3 - 5, 2018? Grab your ticket today and use the promo code "FOCUS" to get The Works for only $399. bit.ly/2okDq8i
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We're excited to be nominated for 2018 #BestPlacesIN and #MiraAwards -- join the team, check out job openings bit.ly/2oi7Zvq
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