Russ King

President of MethodSense, a Life Science service company focused on the convergence of Quality, Regulatory Affairs and Technology. #meddevice #biotech #pharma

[Russ King @RussKing3]

Thanks to @SGottliebFDA for keeping us posted regarding the @FDA shutdown plans. https://t.co/qes0FSxI6h

[Russ King @RussKing3]

Learn #FDA 2018 priorities, which will be helpful if you're planning to submit a device for US clearance in 2018. https://t.co/tri7Ue9hMV

[Russ King @RussKing3]

Starting this month, #MedicalDevice companies are required to pay a 2.3% medical device excise task.

https://t.co/IVjZXgvHAZ

[Russ King @RussKing3]

Get MethodSense's latest Tips & Tools for Medical Device Companies https://t.co/UvIAz90fi8

[Russ King @RussKing3]

Planning to bring a product to market in the US this year? #FDA 2018 MDUFA fees will be enforced soon. https://t.co/bxtJICXzmT

[Russ King @RussKing3]

Check out this month's Tips & Tools from #MethodSense #IEC62304 #humanfactors https://t.co/hXLMBYdBO7

[Russ King @RussKing3]

What does it mean that #FDA has streamlined their process for recognizing consensus standards? Learn more => https://t.co/IcKZB10F7Z

[Russ King @RussKing3]

@CIOApplications recognizes MethodSense as Top 25 Life Science Technology Vendors #RegulatoryConsulting #Compliance https://t.co/PkdPFZHToG

[Russ King @RussKing3]

Catch up on recent Quality & Regulatory news from #MethodSense https://t.co/AT7pobu7dW

[Russ King @RussKing3]

MethodSense's senior #FDA #regulatory strategist named female CEO of the year. Check out her success story: https://t.co/f9eqYrhCjO

[Russ King @RussKing3]

FDA envisions digital health unit will monitor & implement use of real world evidence to support regulatory process https://t.co/4HMFsFPzKm

[Pannam Imaging @pannamimg]

What are the best sites for the latest on Medical Technology? https://t.co/ONXHvOpdgd w @MPOmagazine @jamasoftware @ThePatentProf @RussKing3

[Russ King @RussKing3]

Find out 10 things you need to know about #HumanFactors for your #MedicalDevice to satisfy #regulatory requirements https://t.co/tWQ00840L4

[Russ King @RussKing3]

Learn how @US_FDA is approaching cybersecurity to minimize the potential threat of medical device hacking. https://t.co/GbzvzG49Ok

[Russ King @RussKing3]

Good read about #digitalhealth and #bigdata https://t.co/PTTDNkNPzC

[GE HealthCare @GEHealthCare]

How we can transform data into insights to improve lives globally? Opinion from two #digitalhealth experts https://t.co/DvvoJazbsx

[Russ King @RussKing3]

One of the big questions from the #CuresAct is how will it affect #medicaldevice software? Find some answers here: https://t.co/TmaUECtdy1

[Russ King @RussKing3]

@POTUS signs #CuresAct into law. Here's how it impacts #FDA and #medicaldevice companies. https://t.co/FCsjxXonrY

[Russ King @RussKing3]

@FDAinspections We provide #quality and #regulatory support for #lifescience and #medicaldevice companies https://t.co/WIE6fKseWJ

[Russ King @RussKing3]

Get insight on Human Factors Engineering and FDA requirements for medical devices https://t.co/nq8NWKSWvP

[Russ King @RussKing3]

Guidance on how to transition your #medicaldevice company from #ISO13485 :2003 to #ISO13486:2016 https://t.co/0l6fCn77gD