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The Compliant Path

@sushvin-consultancy-services

Experts in Medical Devices Quality & Regulatory Compliance

45 posts

sushvin-consultancy-services

Aug 11

Global medical device regulatory roundup for July 2026 — covering MHRA, EU MDR/MDCG, Team-NB surveillance, FDA, TGA, Swissmedic, CDSCO, and

#MedicalDevices #MedicalDeviceCompliance #RegulatoryUpdates #MedTech #MedicalDeviceRegulatory #MDR #IVDR #MHRA #FDA #CDSCO #MedicalDeviceSoftware #UDI #RiskManagement #ISO14971 #ISO24971 #HealthcareRegulatory #MedicalDeviceIndustry

sushvin-consultancy-services

Jul 23

Everything cosmetics brands need to know about drafting a CPSR and assembling a Product Information File under EU & UK regulations in 2026.

#Cosmetic Compliance #CPSR #Cosmetic Safety #Product Information File #CosmeticCompliance #sushvin.com #sushvin consultancy

sushvin-consultancy-services

Jul 8

Stay updated with the latest global medical device regulations including MHRA, FDA, EU MDR, EUDAMED, eIFU, AI medical devices, UDI Australia

#sushvinconsultancy #medical devices #medical devices industry #fda #medicaldeviceregulations #compliance #eifu

sushvin-consultancy-services

Jun 12

Understand the strategic implications of the new EU regulation on electronic instructions for use (eIFU) for medical devices. Explore the co

#MedicalDevices #eIFU #EU Compliance #MDR #IVDR #RegulatoryAffairs #HealthcareTechnology #Digital Documentation

sushvin-consultancy-services

Jun 10

Explore the importance of global medical device vigilance management, including safety monitoring, incident reporting, and post-market regul

#MedicalDeviceVigilance #RegulatoryCompliance #PostMarketSurveillance #PatientSafety #MedicalDevices #sushvinconsultancy #medicaldeviceregulations #medical devices industry

sushvin-consultancy-services

Jun 9

Explore May 2026 medical device regulatory updates from the UK, EU, USA, Australia, Malaysia, Team-NB and ISO, including MDR, IVDR, UDI, lab

#sushvinconsultancy #medical devices #medicaldeviceregulations #iso updates #mhra #compliance #fda #ISO

sushvin-consultancy-services

May 11

Get the latest medical device regulatory updates for April 2026 — MHRA UK fee changes, EU MDR MDCG guidance, MIR Form 7.3.1, ISO 14155:2026,

#sushvinconsultancy #medical devices industry #mhra #medicaldeviceregulations #fda #SAHPRA #IMDRF #iso updates #CDSCO #CDSCO Updates #Health Canada Updates

sushvin-consultancy-services

Apr 9

Explore March 2026 medical device compliance updates from Sushvin, including TGA software-based medical device exclusions, ISO 20417:2026, a

#sushvinconsultancy #medical devices #medicaldeviceregulations #fda #medical devices industry #compliance #TGA #uk updates

sushvin-consultancy-services

Mar 9

Stay updated with Sushvin Consultancy's the latest medical device regulatory and compliance updates for February 2026, including FDA guidanc

#medical device compliance updates #medical device regulatory updates 2026 #FDA medical device guidance 2026 #clinical decision support software regulation #medical device global regulatory updates #healthcare compliance news #digital health regulatory updates #TGA medical device regulations #Sushvin Consultancy Newsletter

sushvin-consultancy-services

Feb 16

Learn how FDA’s QMSR 2026 replaces QSR and aligns with ISO 13485. Understand key changes, inspection updates, compliance impact, and prepara

#FDA #QMSR #Medical Device #Quality Management #Regulations #Compliance #ISO 13485 #sushvinconsultancy #medical devices #What is QMSR 2026?

sushvin-consultancy-services

Feb 9

January 2026 medical device compliance updates covering FDA wellness & CDS guidance, EU EUDAMED and ISO standards, Australia TGA consent to

#sushvinconsultancy #HongKongMDACS #AustralianMedicalDeviceRegulation #EUMDRIVDRUpdates #medical devices #medical devices industry #mhra #medicaldeviceregulations

sushvin-consultancy-services

Jan 22

Compliant sterilisation validation services for medical devices supporting ISO standards, EU MDR, FDA, and Notified Body audits.

#sushvinconsultancy #medical devices #medical devices industry #medicaldeviceregulations #Medical Devices Sterilisation Validation Services #us fda #EU MDR #notified body #ISO #FDA

sushvin-consultancy-services

Jan 16

Key FDA, EU MDR, EUDAMED User Guide, SFDA, IMDRF, ISO & MDSAP medical device compliance updates for December 2025. Stay audit‑ready with Sus

#sushvinconsultancy #medicaldevices #compliance #regulatory #MedicalDeviceComplainceUpdates #MonthlyNewsletter #EUDAMEDUserGuide #EMA December 2025 #Saudi Food and Drug Authority Updates #SFDA Updates #IMDRF #Council for International Organizations of Medical Sciences

sushvin-consultancy-services

Jan 13

Explore MDCG 2025-10 post-market surveillance recommendations for medical devices & IVDs. Includes PMS plans, risk analysis, QMS links, and

#sushvin consultancy #MDCG #pms #uk medical device regulations #medical devices #in vitro diagnostic devices (IVDs)#Post-Market Surveillance

sushvin-consultancy-services

Dec 29, 2025

Learn about the European Commission’s transformative 2025 medical device regulation reform (COM (2025)1023), including streamlined MDR/IVDR

#European Commission Proposal Com (2025) 1023 #EU MDR reform 2025 #IVDR proposal COM (2025)1023 #medtech compliance 2025 #MDR IVDR transition support #Sushvin Consultancy #Medical Device Complianc

sushvin-consultancy-services

Dec 9, 2025

Sushvin Consultancy's Nov 2025 Medical Devices Compliance & Regulatory News explains EUDAMED roll-out, PMCF debates, and digital label trend

#sushvinconsultancy #medical devices industry #compliance #medicaldevices #ivdr #medicaldeviceregulations #EUDAMED #PMCF

sushvin-consultancy-services

Nov 7, 2025

#sushvinconsultancy #medicaldevices #medical devices industry #regulatory #compliance #MedicalDevicesRegulatoryUpdates #FDA #QMSR #MHRA

The Compliant Path @sushvin-consultancy-services - Tumblr Blog | Tumgag