CDMC utilizes state of the art technologies combined with decades of practical experience to offer a complete range of clinical data management, analysis and reporting solutions for some of the most prominent pharmaceutical and
biomedical companies.
More... |
SubmIT handles the complete
submission process throughout the
product lifecycle. We provide a wide
range of regulatory services
including document management,
dossier compilation, publishing,
amendment management and
communication with the authorities -
streamlining the process of
compiling new submissions as well
as upgrading legacy submissions
to conform to CTD/eCTD.
More... |
inPACK specializes in secondary and
primary packaging of investigational
medicinal products and offers clinical
supply solutions. The packaging and
storage are carried out in a
controlled, monitored and GMP
certified facility, with a professionally trained team and an air-tight QA process – thus ensuring our customers the most professional and reliable service. inPACK addresses all study types
More... |
ClinCore plans, establishes and runs clinical trials at trial sites. We assist sponsors and investigators in
achieving the goals of the study.
ClinCore is committed to meeting the highest standards of quality while maintaining the safety and welfare of the trial participants. By adhering meticulously to GCP guidelines, regulatory requirements and ethical standards we enhance the trial’s reliability.
More... |