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Guide to FDA and EU Medical Device Regulations 2017 Edition
NEW for 2017 — You’ll get the full text (more than 1,000 pages) of the European Union’s newly revised regulations for medical devices and in vitro diagnostic devices.
No matter on which side of the Atlantic you do business, this fully updated and expanded guide keeps you in touch with the medical device regulations you have to follow.
In addition to the full text of the FDA’s regulations in 21 CFR Parts 800 to 898, the 2017 Guide includes more than 150 FDA guidances for devicemakers, covering everything from acceptance and filing review of premarket approval applications to the unique device identification system.
The FDA has released more than 50 new guidances since publication of the 2015 Guide, including:
List of Highest Priority Devices for Human Factors Review
Reporting of Computational Modeling Studies in Medical Device Submissions
Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling
Software as a Medical Device (SaMD): Clinical Evaluation
Use of Real-World Evidence to Support Regulatory Decision-Making for Medical Devices
FY 2017 Medical Device User Fee Small Business Qualification and Certification
Adaptive Designs for Medical Device Clinical Studies
You’ll find them all here.
Plus, published in PDF format, you’ll be able to perform keyword searches on the entire (5,000+ pages) Guide as well as pick and choose the documents you need to reference and even print and disseminate them to your staff.
For newcomers and veterans alike, this is a must-have quick-reference encyclopedia.
Stay up-to-date on key medical device regulations with Guide to FDA and EU Medical Device Regulations, 2017 edition — the most authoritative and comprehensive guide ever assembled.
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PDF Edition
Available Format
PDF Edition — $397
Who Will Benefit
Regulatory affairs/compliance
Quality control
Legal affairs
Supplier management
Clinical research
Software developers/managers
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