Investigator-Initiated Trials
Investigator-Initiated Trials (IITs), often referred to as non-commercial clinical trials, predominantly address questions that have arisen from medical treatment practice. IITs, like pharma-sponsored (commercial) clinical trials, fall under the definitions and regulations of the German Medicines Act (AMG), the German Regulation on Good Clinical Practice (GCP-V) and EU legislation. In order to deepen her knowledge […]
How to increase your conflict competence
One of our Project Leaders will participate in the intensive course “Conflict Management – Systematically increase your conflict competence” from 03 to 05 July 2013 in Stuttgart, Germany. Everyday work is never entirely free of anger, disagreements, tensions or differences of opinion. In this respect, particularly project managers must succeed in mediating between the different […]
Sharing experiences with the biotech industry
The “German Biotechnology Days” is the national forum where Germany’s biotech industry meets to share experiences. This year, it is held on 14 and 15 May in Stuttgart. One of our Business Unit Directors will participate. The “German Biotechnology Days” were initiated by the German Federal Ministry of Education and Research (BMBF) in 2010 and […]
Training event on the FSA Code of Conduct
At an internal training event imparted by one of ClinTriCare’s Business Unit Directors, our employees familiarized themselves with the content and “spirit” of the Code of Conduct for Healthcare Professionals issued by the German Voluntary Self-Regulation Body for the Pharmaceutical Industry (FSA) All participants completed the training with a certificate. The FSA website states about […]
Pneumology in flux
From 20 to 23 March 2013, one of our Project Leaders will attend the 54th Congress of the German Society for Pneumology and Respiratory Medicine, the most important national forum for the exchange of the latest scientific findings on respiratory diseases. This year, the DGP Conference will be held in Hanover under the motto “Pneumology […]
Continuing education as a sign of quality
One of our Senior Project Coordinator will participate in the seminar “Quality Management in Clinical Research” in Mannheim on 12 March 2013. The objectives of the seminar are to convey the basics of quality management in all phases of a clinical trial and to share helpful information on how to conduct audits. Details on the […]
Regulatory requirements always on the radar
“As a project manager in clinical development, I always have the interaction with the regulatory department on my radar. This allows me to identify any risks to regulatory approval early on in a project. To do that, of course, you have to know the drug approval procedures.” This is the answer given by a ClinTriCare […]
Regulatory update
Up-to-date information on important new regulations is provided by the annual symposia of the German Federal Association of Contract Research Organizations (BVMA). “Drug research on humans: With patients, for patients” – this is the motto of this year’s symposium on 23 November 2012 in Munich. The program is available at www.bvma.de. A ClinTriCare Project Leader […]
Project management in clinical trials
One of ClinTriCare’s Project Leaders will be a speaker at the seminar organized by Akademie Heidelberg entitled “Project Management in Clinical Trials – Basic Course” on 11 and 12 September 2012 in Munich, Germany, where he will teach the basics of project management and highlight the challenges faced by project leaders in pharmaceutical and biotech […]
Update on diabetes mellitus research
From 01 to 05 October 2012, one of our company’s Project Leaders will attend the “48th Annual Meeting of the European Association for the Study of Diabetes”, the largest and most important European meeting for the exchange of the latest scientific findings concerning diabetes mellitus. A central element of this year’s event in Berlin will […]