ClinStorage
ClinStorage AB is a leading provider of GMP and GDP certified storage, clinical trial services, and biobank solutions. Founded by Ola Camber and Sven Jacobsson, the company specializes in ultra-low temperature storage, sample handling, and distribution for pharmaceutical and biotech companies. With extensive experience and certifications, ClinStorage supports global research organizations with secure storage, sample management, and regulatory compliance, aiming to facilitate safe and efficient development of medicines.
Industries
Nr. of Employees
small (1-50)
ClinStorage
Products
Cloud-based biobank data manager (LIMS)
A cloud-hosted, platform-independent laboratory information management application for biobanks providing mobile sample logging, freezer-position mapping, barcode scanning and basic EHR/CRF data capture.
Cloud-based biobank data manager (LIMS)
A cloud-hosted, platform-independent laboratory information management application for biobanks providing mobile sample logging, freezer-position mapping, barcode scanning and basic EHR/CRF data capture.
Services
Storage of pharmaceutical and biological materials across temperatures from room temperature to vapor-phase liquid nitrogen with continuous monitoring and redundant backup systems.
Management of global distribution, transport coordination and cold chain logistics for investigational medicinal products to clinical trial centres.
GMP-certified secondary packaging and labelling performed in controlled temperatures (examples: -20°C, +5°C, room temperature) for investigational medicinal products.
Batch certification and Qualified Person release of IMPs (sterile, non-sterile and biological), plus importer-of-record services and handling under Manufacturing and Import Authorization.
Reception, inspection, aliquoting/dispensing, position-based storage, sample retrieval and tailored dispatch for clinical study samples.
Management and preparation of cryogenic and dry-ice shipments, including use of dry shippers and documented handling procedures for temperatures below -150°C.
Storage of pharmaceutical and biological materials across temperatures from room temperature to vapor-phase liquid nitrogen with continuous monitoring and redundant backup systems.
Management of global distribution, transport coordination and cold chain logistics for investigational medicinal products to clinical trial centres.
GMP-certified secondary packaging and labelling performed in controlled temperatures (examples: -20°C, +5°C, room temperature) for investigational medicinal products.
Batch certification and Qualified Person release of IMPs (sterile, non-sterile and biological), plus importer-of-record services and handling under Manufacturing and Import Authorization.
Reception, inspection, aliquoting/dispensing, position-based storage, sample retrieval and tailored dispatch for clinical study samples.
Management and preparation of cryogenic and dry-ice shipments, including use of dry shippers and documented handling procedures for temperatures below -150°C.
Expertise Areas
- GMP/GDP-compliant biorepository storage
- Cold chain logistics and cryogenic shipping
- Clinical supply services and IMP secondary packaging
- Qualified Person (QP) batch release and MIA/importer-of-record handling
Key Technologies
- Vapor-phase liquid nitrogen storage
- Ultra-low temperature freezers (-80°C to -196°C)
- Dry shipper cryogenic transport
- Dry ice shipment procedures
News & Updates
Achieved over 100 receptions/dispatches in one month (October 2022), including packaging, labelling, and QP release of investigational medicinal products across the EU.
Achieved over 100 receptions/dispatches in one month (October 2022), including packaging, labelling, and QP release of investigational medicinal products across the EU.