SanaClis is a full-service Global CRO with a fully integrated clinical supply chain, thereby offering a comprehensive range of end-to-end services for clinical trials. SanaClis was founded in 2000 by seasoned industry experts, all of whom have had executive level positions in leading pharma companies and large global CROs.
SanaClis has vast experience of successfully running studies for various sized sponsors, ranging from virtual biotech’s through to top ten pharma companies, both in terms of its CRO services and Clinical supply services. Every project is a fundamental priority for the SanaClis, irrespective of the size or scope. SanaClis believes that every company and professional should receive an extremely high level of quality and clinical excellence applied to its projects. SanaClis prides itself upon its esteemed track record of successfully delivering various projects on time and on budget, ensuring quality, expertise and responsiveness resonates throughout the entire project duration.
Whilst SanaClis offers the provisions of our services across all therapeutic areas and geographic locations (entire Europe, USA, UK and Asia), SanaClis has a substantial and unique expertise in Central and Eastern European countries, regions of which provide an abundance of advantages, from high recruitment rates through to high quality of data. In addition to being a full service CRO, SanaClis is one of the very few service providers with an extensive range of in-house logistics and clinical supply capabilities. SanaClis has a portfolio of privately owned GMP and GDP certified storage and distribution depots, strategically located across the EU and CEE regions.
Full end to end in-house CRO services include:
- Project management
- Regulatory
- Monitoring
- Data management and biostatistics
- Medical writing
- Pharmacovigilance
Further end to end in-house supply chain services include:
- QP services (EU QP release)
- customs brokerage
- GMP warehousing and distribution services (at all required temp conditions, ambient, cold, frozen, cryo etc), packaging and labelling, controlled substance license
- sourcing of clinical trial materials including ancillaries, PPE, comparators, generics and rescue medication sourcing.
- IOR imports and exports
This unique and fully comprehensive service offering allows SanaClis to streamline the entire project from end-to-end, thereby creating cost efficiencies, whilst maintaining a high level of quality at all times and adhering to agreed timelines
