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From CDASH to ADaM – Professional Data Management in Clinical Trials!

News of July 20th, 2023
20.07.2023

We are pleased to announce that AGAH (Arbeitsgemeinschaft für Angewandte Humanpharmakologie e.V.) is once again offering the very successful hands-on workshop on Clinical Data Management (CDM) and our experts will again contribute to this event. Especially in early clinical trials of phases I/II, study planning should include CDM principles from the very beginning to ensure robust and reliable results in the end. Therefore, a sound understanding of data structures and knowledge of CDISC is essential. 

New to the workshop: the interface between CDM and Pharmacovigilance!

Let our experts guide you through the world of CDASH, UAT, Define-XML etc. as well as through interactive sessions focusing on eCRF. 

Take advantage of this exciting one-day workshop and register today: Registration - Applied Course in Clinical Data Management
For more information, see AGAH - Applied Course in Clinical Data Management

Socrametrics News

New GCP Training Courses now available at SocraTec R&D

20.07.2023

Our sister company SocraTec R&D has now added GCP training courses to their service portfolio.


From now on you can book the following training courses through their website:


Grundlagenkurs für Mitglieder eines Prüfungsteams bei klinischen Prüfungen nach der Europäischen Verordnung (EU) Nr. 536/2014 (Humanarzneimittel)


Aufbaukurs für Prüfer und Hauptprüfer bei klinischen Prüfungen nach der Europäischen Verordnung (EU) Nr. 536/2014 (Humanarzneimittel)


So if you are interested in taking these classes, go to the SocraTec R&D website to learn more. The first GCP training alreday starts in May 2023.


https://socratec-pharma.de/services/gcp-courses

Socrametrics News

We will answer your questions regarding this topic.
Juliana Brudel is at your disposal.

SocraMetrics now offers full-scope Pharmacovigilance Services!

News of August 1st, 2023

New service - SocraMetrics has extended the service portfolio and now provides professional level pharmacovigilance and vigilance services for pharmaceutical companies worldwide from clinical trials to marketing! 

For national and international trials we now offer the full package of pharmacovigilance services. Our highly qualified team also acts as the person responsible for pharmacovigilance for the pharmaceutical company (EU-QPPV, UK-QPPV, Graduated Plan Officer in Germany).

For more details see here.