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EU regulation for in vitro diagnostics
Although 2021 has only just begun, manufacturers of in-vitro diagnostics must already look to 2022, when the current IVD directive will be replaced by an EU-wide regulation. On May 26, 2022, the...
New biobanking standard ISO 21899 published
The biobanking standard ISO 21899, "Biotechnology - Biobanking - General requirements for the validation and verification of processing methods for biological material in biobanks", was published in...
Presentation of the BioARCHIVE software using the example of the research project Clinical-Virology-Net (CVN)
program and registration agenda Moderator: Dr. Norbert Schmeisser, Managing Director, MEDEORA GmbH 16:00 Welcome by the BioRiver working group IT Dr. Constanze Duhme, BioRiver eV Sibylle Ohm,...
Review: BioRiver working group IT – digitization of processes
The fourth meeting of the IT working group on November 3rd, which again took place as an online meeting, dealt with the digitization of processes. The two presentations made the broad spectrum of...
Invitation: Digitization of processes on November 3rd, 2020 at the 4th digital meeting of the BioRiver working group IT
The biobanking standard ISO 21899, "Biotechnology - Biobanking - General requirements for the validation and verification of processing methods for biological material in biobanks", was published in...
Specialist event “LIMS Forum” in November with a 10% discount
From 9th to 10th The LIMS Forum will take place again this year on November 1st. The event is aimed at decision-makers and IT users from companies and laboratories who are looking for...
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