Chrondel's teams act as a bridge between the Sponsor, CRO and the site to take each and every trial faster to next level.
Chrondel provides experienced research staff according to your study specific needs in different levels/roles
At research sites: site coordinator, study nurse, technician, trainer and auditor
For the industry: CRA, Project manager, trainer and auditor
Our training experience, research expertise and robust IT infrastructure enables us to partner with research sites, investigators and hospital management to leverage site activities, performance, efficiency and quality.
Chrondel enables you to collaborate within flexible working models (fulltime, part-time, project based)
Thanks to its ancillary supply management and local procurement abilities, Chrondel provides sourcing, maintenance, return and destruction including warehousing when needed for;
Equipment (i.e freezers, temperature monitoring devices and passive shippers).
Chrondel also supports calibration services in selected countries to enhance the standardization of your trial.
With its strong network of trainers both in-house and external; Chrondel provides trainings on following areas:
Country Specific Regulations
Quality System Management
By its vast experience and infrastructure on quality management and IT services, Chrondel may be your partner in transformation of hospital units into research centers. As a journey walked together, Chrondel will not only be a consultant, but a partner and may help on;
Audits and gap identification
Quality System Establishment & Implementation
Study Coordinator - Study Nurse Staffing
Transformation of clinics into research sites
Sourcing Clinical Trial Materials
Chrondel adds value to the clinical research conducted by the Sponsors by maximizing patient enrollment, data quality, accuracy as well as optimizing timelines.
Inspired by Swiss research culture, we believe our code of conduct, systemic approach and patient centricity secure the success of clinical trials outcome
Proper site management plays a key role for successful patient recruitment and compliance to GCP guidelines; thus for the success of clinical trial deliverables without interruption. In Chrondel, we believe that this can only be achieved by real team work combined with technical knowledge and expertise.
All services managed by qualified professionals in accordance with the ICH-GCP, cGMP-annex13, GDP as well as national and international laws/regulations.
Takes advantage of extensive experience as the pioneer of the industry and advanced know-how
reflecting Swiss research culture.
Provides temporary/permenant solutions for your research infrastructure needs
Supports research centers on quality systems to keep them always up-to date and thus to leverage up in competition