Study protocols designed for ethical drugs and medical devices to be successfully granted a marketing authorisation.
Drive the drug through the administrative red tape and health products related legislation. Reap the benefit from the regulatory watch performed by ICTA’s Quality Assurance department.
A management which combines achievement of objectives with the appropriate organisation.
30 years of experience, a set of reactive procedures which stem from systemic analysis and a customizable IT platform for an efficient adaptive monitoring.
A department that combines expertise in descriptive biostatistics, inferential biomathematics and modelisation.
A high value department that combines medical and scientific knowledge, bibliographical expertise and ability to analyse and synthesize results.
An expertise in pharmacovigilance and medical device vigilance oriented security of development
A wide network of hospital CRAs and CSAs with highly developed medical and scientific training well versed in clinical R&D requirements.
