Basket - Journal of Medical Device Regulation

Buy Subscription

“A framework for pre-submission risk screening in medical device regulatory submissions: categorising common FDA deficiency themes” has been added to your basket. Continue shopping

Remove item	Thumbnail image	Product	Price	Quantity	Subtotal
×		Best practices for obtaining breakthrough designation using the US FDA’s Breakthrough Devices Program	£50.00	Best practices for obtaining breakthrough designation using the US FDA’s Breakthrough Devices Program quantity	£50.00
×		Cybersecurity in the USA – developing a NIST SSDF-based Profile for low and moderate risk medical device applications	£50.00	Cybersecurity in the USA – developing a NIST SSDF-based Profile for low and moderate risk medical device applications quantity	£50.00
×		Analysis of the European Commission’s proposal for the revision of the MDR and IVDR	£69.00	Analysis of the European Commission’s proposal for the revision of the MDR and IVDR quantity	£69.00
×		August 2026 - Volume 23, Issue 3	£199.00	August 2026 - Volume 23, Issue 3 quantity	£199.00
×		An overview of the medical device regulations in Jordan	£50.00	An overview of the medical device regulations in Jordan quantity	£50.00
×		Clarifying the role of equivalence and similarity in medical device conformity assessment under the MDR	£50.00	Clarifying the role of equivalence and similarity in medical device conformity assessment under the MDR quantity	£50.00
×		A framework for pre-submission risk screening in medical device regulatory submissions: categorising common FDA deficiency themes	£69.00	A framework for pre-submission risk screening in medical device regulatory submissions: categorising common FDA deficiency themes quantity	£69.00
Coupon:

Basket totals

Subtotal	£537.00
VAT	£0.00
Total	£537.00

Proceed to checkout

Click here to continue shopping