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Newsletter

Latest News Updates

Stay ahead in the medical device industry with our April 2025 newsletter!

Medical Devices Industry Updates Newsletter May 2025

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Stay ahead in the medical device industry with our April 2025 newsletter! Key updates from MHRA and EU regulations, new advisory services, and more.

Medical Devices Industry Updates Newsletter April 2025

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Medical Device Compliance in 2025 and Regulatory Changes

Medical Devices Industry Updates Newsletter March 2025

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Device Compliance in 2025: Are You Ready for MHRA and EU Changes?

Medical Devices Industry Updates Newsletter February 2025

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From Compliance to Innovation:New Medical Device Rules in the UK, Australia & EU for Medical Devices

Medical Devices Industry Updates Newsletter January 2025

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Medical Devices Industry Updates Newsletter December 2024

Medical Devices Industry Updates Newsletter December 2024

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Medical Devices Industry Updates Newsletter November 2024

Medical Devices Industry Updates Newsletter November 2024

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Medical Devices Industry Updates Newsletter October 2024

Medical Devices Industry Updates Newsletter October 2024

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Medical Devices Industry Updates Newsletter August 2024

Medical Devices Industry Updates Newsletter September 2024

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Medical Devices Industry Updates Newsletter August 2024

Medical Devices Industry Updates Newsletter August 2024

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MHRA Announces A Proposed Framework For International Recognition of Medical Devices.

MHRA Announces A Proposed Framework For International Recognition of Medical Devices

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Discover Our Range of Services

Sushvin provides a wide range of services designed to cater to the diverse needs of our clients. Our extensive service offerings include:

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mdr 2017, MDR 2017/745, mdr compliance, medical device post market surveillance,
medical device quality consultancy, medical device quality consulting, medical device regulation, medical device regulatory consulting, medical device regulatory consulting services, medical device regulatory services, medical device regulatory services in uk, medical devices rules 2017

Medical Device Regulation 2017/745

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Medical Device Quality Assurance & Compliance, ISO13485: 2016 Quality Management Services, Medical Device Regulation 2017/745 QMS Transition

Quality Assurance And Compliance

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Auditing Solutions, Intenal Audit

Auditing Solutions

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brexit transition, brexit transition period, brexit transition period end date, eu and brexit, eu brexit

Brexit Transition

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PRRC - Person Responsible For Regulatory Compliance, Medical Device Registrations, UK Registration, Global Registration, MDSAP (Medical Device Single Audit Program)

PRRC - Person Responsible For Regulatory Compliance

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UK Responsible Person, UKRP, legal medical device/IVD, UK MDR 2002

UK Responsible Person

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medical device regulatory services, medical device regulatory services in uk, medical devices rules 2017

Medical Device Registrations

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PMS - Post Market Surveillance/PMCF,

PMS - Post Market Surveillance / PMCF

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Clinical Evaluation Reports (CER)

Clinical Evaluation Reports

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Software As A Medical Device, MDR 2017/745 and IVDR 2017/746

Software As A Medical Device

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registration applications for drug device combination products, Combination Drug Device Support

Combination Drug Device Support

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