David DeRam

The Ultimate Guide to Corrective and Preventive Action (CAPA) for Medical Devices Companies bit.ly/2A5ZfwN by @greenlightguru

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

Free Webinar: Everything Device Makers Need to Know About Design Controls bit.ly/2FUThk0 hosted by @medicalmarcom & the 350k+ LinkedIn Medical Devices Group

Greenlight Guru Launches New Software, Growing Team: ow.ly/BqyG30jSrsB #IIBTV @greenlightguru @TechPointInd @GerryDick

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!

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/310143

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

Why I Only Hire People With 'Alligator Blood' | by @DeRam_David entm.ag/2yj

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

"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

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

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

We're excited to be nominated for 2018 #BestPlacesIN and #MiraAwards -- join the team, check out job openings bit.ly/2oi7Zvq