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Home
Blog
Blog
17 February 2023
ViSU
What EU MDR changes mean to Manufacturers & what’s Next !
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11 August 2022
ViSU
China UDI Requirements
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11 July 2022
ViSU
Medical Devices: Structured Content Authoring Saves Time & Reduces Cost
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5 May 2022
ViSU
5 Challenges of Medical Device Content & Solutions
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19 September 2022
ViSU
Regulatory Managers Increase Flexibility without Losing Productivity
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2 April 2021
ViSU
Current Alternatives To EUDAMED
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25 September 2020
ViSU
UDI & EUDAMED Explained under EU MDR
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11 February 2020
ViSU
Most Common and Avoidable Mistakes While Adopting ISO 13485
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31 January 2020
ViSU
Regulatory Data and Info Management for Med Device Success
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28 November 2019
ViSU
Effective Regulatory Change Management with Reg Intel Equipped RIM Tech
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21 October 2019
ViSU
Reg Information/Data for Devices, very important going forward!
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13 March 2019
ViSU
Digitize Instructions for Use (IFU) to Comply with EU MDR
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