Certified Lead Auditors

CIMS is CQI/IRCA(1) certified as lead auditors within ISO 9001:2015(2) to support our domain specialty of the drug development process and data sciences.  We use the Quality Management Systems (QMS) as the foundation for the drug development process establishment, continuous improvement and anchoring.  The QMS will be the centre point of our data Læs mere…

Outsourcing has become a significant risk

Take back control over your data Risk Based selection of clinical data process elements requires insight in the full process Information collection and controlling information flow, data models, analysis, process, systems integration, regulatory requirements, statistical methods, knowledge management, Quality Assurances and Control, CRO integration, Patient Safety and GVP, Cost reduction, Læs mere…

CIMS Reporting Apps

Tracking of Operational progress and development depends upon quality data and it’s availability CIMS Reporting Apps establish the connections needed CIMS reporting Apps is integration between Company process Planning KPI integration Apps deployment Establish reporting functions for all layers in the company Monitoring Progress and Quality FSP integration CIMS Report Læs mere…

Data Protection System

Ensures you are in compliances with GDPR when working with vendors outside EU Also, when subsidiary parties to your vendor are processing your data GDPR data exchanges control outside EU can be very cumbersome and very worrying. Transfers of personal data to third countries are regulated under Articles 44-50of the Læs mere…

Clinical Informatic

If you control your data you control your studies and programmes CIMS Clinical Informatic is:Knowing where every piece of data is at a given timeKnowing who needs what information at what timeLearning from data continually and foresee obstacles before they happenEnabling and facilitate control CIMS Clinical Informatic in context Clinical Læs mere…