Regulatory News Archives - Page 2 of 2 - Arazy Group Consultants Inc.

Unique Device Identifier (UDI) Submission as part of Pre-Market Requirements

by arazygroup | Jul 9, 2021 | Blog, Regulatory News Slider

As part of IMDRF Key Objectives 2021-2025 (Committee, 2020), the utilization of Unique Device Identifier (UDI) System is deemed as important to standardize information collected by regulators via post-market surveillance activities. The United States Food and Drug...

LICENSALE Mobile Now Available!

by arazygroup | Apr 14, 2022 | Blog, Case Study, Regulatory News Slider

Medtech Registration Just Became Mobile LICENSALE® Mobile is now available on the App Store and Google Play. Login with your portal registration credentials to view your registration projects from anywhere. MARKETING STATUS View your products’ real-time...

UK MHRA: Regulating Medical Devices Starting January 1st, 2021

by arazygroup | Sep 10, 2021 | Blog, Regulatory News Slider

Regulatory Update: New Guidelines of UK MHRA The UK MHRA published a new set of guidelines related to the UK medical device regulations starting from January 1st, 2021. From January 1st 2021, the Medicines and Healthcare products Regulatory Agency (MHRA) will be the...

Unique Device Identifier (UDI) Submission as part of Pre-Market Requirements

LICENSALE Mobile Now Available!

UK MHRA: Regulating Medical Devices Starting January 1st, 2021

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