Gert Bos
@gertwbos
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Healthcare RA professional interested in change management, improving systems & regulations, maintaining an efficient innovative environment - my personal views
at the Heart of Europe
Joined December 2009
A few days left to sign up for EU-IVDR training. Great weather here in Nanjing Look forward to meeting you there!
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Did you already register for the ABHI conference in October? No time to waste! https://t.co/23tjzGxoh4
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Brexit day, 10 months to g; levels of uncertainty is rising. Key day in Brussels today as input in risk management. https://t.co/LIMIg8nujv
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Last minute request for Jaap Noordmans to speak on GDPR implementation, also in relation to upcoming MDR regulation. https://t.co/ORh3ABTCI3
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Possible opportunities for fast track innovative devices in special section of China. Read today's blog from Minghua Chen. https://t.co/KludhhB8ht
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if you have not signed up to our newsletter, this is what you are missing this publication ;-) https://t.co/fvU0ofSazj
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Great topic, great tutor. When working with stand alone software and with complex embedded software, this focused EU MDR training on developing hardware and software in the new EU regime is a must! Join Rene in this 3 day seminar! https://t.co/nnWYLCALzA
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UDI requirements in CHina inching closer! Read the Blog from Minghua on the progress that is being made. https://t.co/oduF2vjJeB
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A conference you cannot miss if you want keep your medical devices and IVDs on the EU market! #nograndfathering
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Will ANVISA's acceptance of ISO13485 certificates be the end of MDSAP? - a reflection from our Brazil team Qserve Group
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What better excuse would you find for a trip to Zurich than to visit the upcoming Asia Pacific Device Summit Sep 28!… https://t.co/MlBYZqyfkc
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Dutch Minister of Health Edith Schippers surprises Dutch MDR Trilogue success team in todays Stakeholder meeting, wh… https://t.co/aJxzkgXbXg
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Good to see the compromises found to enhance safety whilst keeping access to market also feasible for the SME's
Delighted after 4 years have reached final agreement with @EU2016NL on #medicaldevices to protect patient safety & support innovation
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The long expected EU legislation on medical devices and in vitro diagnostics is close to reality now. With pre-agree… https://t.co/HnoKwMQifm
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Continuous growth #Qserve: adding a design control expert
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Last few seats available for tomorrows Qserve GroupMedTech roadshow event in San Francisco. If you're interested sen… https://t.co/3bdTjdpCt6
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MDR implementation planning is the next thing: have you started yet? New whitepaper is out.
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