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MedTech Intelligence

Volume 10 Issue No. 38

Business Analysis Combination Products Market Access Operations Product Development Quality/Regulatory
 

MEDdesign

Jothy Rosenberg, Dover MicrosystemsA Security Epidemic:
The Internet of (insecure) Things and the Risk to Medical Devices

By Jothy Rosenberg, Dover Microsystems

As medical technological capabilities increase along with the proliferation of embedded systems and IoT, cybersecurity is becoming a very real risk for the medical industry. While securing the whole medical device industry may seem like an insurmountable task, the combination of education, regulation and technology is a good first step toward protecting our most critical infrastructure from attack.

MedTech Import/Export: Regulations, Procedures, Best Practices - October 24, 2018 - Washington, DC

Featured Articles

Kate Leith, Oriel STAT A MATRIXYou can do it!
Nailing Your MDSAP Audit and Sustaining Long-Term Compliance

By Kate Leith, Oriel STAT A MATRIX

A guide to what to expect during your certification audit and how to prepare.

FDAFDA Awards $6 Million in Grants for Pediatric Device Development

By MedTech Intelligence Staff

Innovators will also receive guidance in the areas of prototyping, engineering, IP, testing, grant-writing and clinical trial design.

MedTech M&A: Regulatory & Quality Due DiligenceMedTech M&A:
Regulatory & Quality Due Diligence
A conference brought to you by MedTech Intelligence.

The medical technology industry is witnessing a growing number of mergers and acquisitions, and this poses a unique set of challenges when it comes to due diligence.

 
 

Apple logoApple Watch 4 Gets
FDA Clearance

By MedTech Intelligence Staff

The product can conduct electrocardiograms and measure the heart’s rhythms.

Anura Fernando, UL Life & Health SciencesBeyond Cybersecurity

By Anura Fernando,
UL Life & Health Sciences

As standards around interoperability emerge, now may be the time to look at the benefits of connected technologies.

 

More Articles »

MedTech M&A: Regulatory & Quality Due Diligence

Sponsored Resources
 

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Upcoming Events & Webinars

Oct. 2018October 22-23, 2018 - Med Tech M&A: Regulatory & Quality Due Diligence
Washington, DC

Oct. 2018October 24, 2018 - MedTech Import/Export: Regulations, Procedures, Best Practices
Washington, DC

Nov. 2018November 27-28, 2018 - EU MDR Implementation Strategies Workshop
Washington, DC

Nov. 2018November 29-30, 2018 - Advanced CAPA and Root Cause Analysis Workshop for Medical Device Companies
Washington, DC

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