Our training courses have been awarded
the national Qualiopi certification…
…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.
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.
17-18 Oct 2023 Building on the success of its long-running US-based counterpart, the 6th Annual SCOPE Europe: Summit for Clinical Ops Executives is a two-day executive conference serving clinical innovation leaders, clin ops execs, digital leaders, functional heads, category managers, and those responsible for the planning and management of clinical trials in Europe and the […]
Biopharm International On Sept. 21, 2023, FDA released a new guidance on how the agency plans to utilize alternative tools to remotely evaluate drug manufacturing facilities identified in a marketing application. The application may be a new drug application, an abbreviated new drug application, a biologics license application, or a supplement to any of these […]
Applied Clinical Trials While many US-based biopharma start-ups are interested in conducting clinical trials in Europe, they are often unfamiliar with European legislation and regulations. Some of the biggest misconceptions are around start-up timelines. Typically, the time it takes to go from initial clinical trial application to delivering the first dose to a patient takes […]