Blog Posts | VITROBIO Medical Devices

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All You Need to Know About Allergic Rhinitis: Symptoms, Causes and More

in Scientific news

If you've ever been halted mid-spring by bouts of incessant sneezing, felt your eyes water up at the sight of that blossoming tree in your yard, or found yourself surrounded by tissues during those wa...

Confirmation letter of certification application framework of regulation (EU) 2017/745

We understand the value of transparent and clear communication with our clients, especially when it comes to compliance with regulatory standards. For all our partners who distribute our medical devic...

GMED

Mar 26, 2024 Regulatory

Vitrobio ISO 13485 certificate

In our ongoing commitment to delivering safe, efficient, and reliable medical devices, we place great emphasis on adhering to globally recognized standards. A key example of this is our certification ...

GMED

Mar 26, 2024 Regulatory

Understanding the Medical Device Regulation (MDR 2017/745): A Transformative Shift in the Medical Device Industry

Exploring the Origins, Implications, and Future Impact of the MDR for Stakeholders in the Healthcare Sector The healthcare landscape is ever-evolving, with regulatory frameworks often adapting to ensu...

MDR

Mar 26, 2024 Regulatory

JAN-23 : Vitrobio Certification Update

2017/745 Regulation (MDR) – Vitrobio Certification Update Vitrobio is already committed to the transition to MDR . An application for certification under Annex XI part A of Regulation 2017/745 has bee...

NEWSLETTER

Mar 26, 2024 Regulatory

OCT-23 : Vitrobio Certification Update, UDI and Changes

2017/745 Regulation (MDR) – Vitrobio Certification Update As we informed you in our July newsletter: Vitrobio is already committed to the transition to MDR. An application for certification under Anne...

NEWSLETTER

Mar 26, 2024 Regulatory

JAN-24 : Vitrobio Certification Update, Management and Ressources

Dear VITROBIO Partners and Clients, The entire Vitrobio team wishes you all the best for 2024 and would like to take this opportunity to thank you for your trust and unwavering support. Our partnershi...

NEWSLETTER

Mar 26, 2024 Regulatory

EC Certificate Directive 93/42/EEC

In our commitment to providing safe and efficient medical devices, we align with internationally recognized standards. One such standard is Directive 93/42/EEC (also known as MDD), a European Union di...

GMED

Mar 26, 2024 Regulatory

Delving into the World of Medical Devices: An Overview with a Focus on Class IIa Nasal and Throat Sprays

Understanding Medical Devices, their Classes, Market Dynamics, and a Deep Dive into the Production of Class IIa Nasal and Throat Sprays Medical devices form an integral part of the healthcare industry...

Mar 26, 2024 Scientific news

Navigating the Transition from MDD to MDR: Legacy Devices and Marketing Authorization

Implications of the Extended Transition Period and How it Impacts Legacy Devices and Their Marketing Authorization The evolution of the regulatory landscape in the medical devices sector has witnessed...

Mar 26, 2024 Scientific news

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