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Home / News



Date: 14-02-2020

MDR implementation date gets close

The Medical Device Regulation was published on 5 May 2017 and came into force on 25 May 2017. Currently approved medical devices will have a transition time of three years (un...

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Date: 28-01-2020

First course Interdos Academy

Recently, we announced to launch our brand new division Interdos Academy shortly. We are proud that we can now officially present you the first course in our curriculum: Funda...

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Date: 23-01-2020

Interdos launches Interdos Academy

2019 has been a year in which Interdos has almost doubled its capacity and expertise in the field of Regulatory Affairs and Pharmacovigilance. We have expanded our team with f...

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Date: 09-10-2019

New regulation Environmental Risk Assessments

As of June 30th 2019, the consultation period has been closed for the draft guideline on the environmental risk assessment of medicinal products for human use. With the update...

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Date: 25-12-2017

New Website

Our company website and leaflet have been modified to reflect the changes. The new company leaflet is enclosed. The new website link www.interdos.nl gives an overvie...

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The Netherlands

Phone: +31 (0)88 255 40 60
You can report suspected adverse drug reactions / side effects of our medicines by sending an email to: pv@interdos.nl

In case of urgent safety issue please contact us: +31 (0)6 511 68 061
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