…a new quality guarantee for training providers in France.
The quality certification has been issued for the following category of action TRAINING ACTIVITIES.
This certification complies with the law of 5 September 2018 “for the freedom to choose one’s professional future”, which imposes mandatory certification according to a single national reference system. Training is a major stake for the quality assurance policies, particularly in the highly regulated sector of clinical research. It is also a key factor in maximising productivity. We provide an expert team to guide and train you.
Download our Qualiopi Certificate
to be independent in designing and configure an eCRF and/or in configuring the related administrative environment. These training courses firstly target data managers and project managers.
enables investigators, CRAs (Clinical Research Assistants), CSTs (Clinical Studies Technicians), etc., to use the software features in an autonomous way.
This training activity is registered under number 11 92 19676 92. It is part of continuous training actions according to the articles L 6313-1 to L 6313-11 of the French Employment Code. It provides financial assistance in the name of continuous professional training.
Number of training certificates issued :
132
Number of training
days completed :
32days
Overall trainee satisfaction rate :
97,2%
If you have any questions about our training program, please do not hesitate to contact our dedicated department by email at
formation-cleanweb@tentelemed.com
Download our rules of procedure
A LEADING POSITION AND
AN INTERNATIONAL DEPLOYMENT
64 +
countries
involved
20 000 +
investigational
Centres
3 million +
patients
in database
50 000 +
users
worlwide
January 30, 2025
MedtechDive Artificial intelligence was a topic of focus for the medical device industry in 2024. Companies including GE Healthcare, Medtronic and Dexcom touted new AI features, and others like Stryker and Quest Diagnostics added AI assets through M&A. Meanwhile, conversations about regulations and generative AI, models that are trained to create new data including images and text, dominated medtech conferences. The Food and Drug Administration recently […]
January 30, 2025
BioPharm International FDA published a final guidance on Jan. 2, 2025 for those interested in participating in the agency’s Advanced Manufacturing Technologies Designation Program, which was developed to facilitate drugs manufactured using advanced manufacturing technologies (AMTs). The guidance, Advanced Manufacturing Technologies Designation Program, is the final version of the draft document issued on Dec. 13, 2023. […]
January 30, 2025
Applied Clinical Trials Online Medable has shared new data from the Tufts Center for the Study of Drug Development (CSDD)’s PACT Consortium linking decentralized clinical trial (DCT) approaches to a higher rate in participation across multiple demographic groups. The new research shows that a more strategic implementation of DCT elements, combined with increased regulatory oversight, […]