CE Marking
Compliance with Regulation (EU) 2017/745 (MDR) and, where applicable, Regulation (EU) 2017/746 (IVDR).
Laboratory Equipment
Laboratory equipment solutions designed to support compliant and efficient clinical trial operations, from study setup to study closeout, ensuring reliable laboratory workflows and operational consistency.
Core laboratory equipment designed to support everyday scientific workflows, enabling efficient sample preparation, routine testing, and reliable analytical processes across laboratory environments.
Solutions designed to ensure reliable temperature control during storage and transport, supporting the safe handling and preservation of temperature-sensitive materials.
Reliable environmental monitoring solutions that provide real-time visibility of parameters such as temperature or humidity, helping safeguard sensitive products and ensure optimal storage and laboratory environments.
Our services
Each laboratory equipment goes through a rigorous preparation process before reaching your investigator sites — so your study can start without delay.
Calibration according to certified standards, with full traceability and calibration certificates.
Protocol-specific setup — parameters, units, alert thresholds — aligned with your study design. Devices arrive ready to use.
Devices configured in the appropriate language for each site, helping ensure smooth adoption and consistent use across your study.
Full functional inspection of every device before shipment to ensure it meets your protocol requirements.
User manuals in the correct language for each site. Documentation archived for 25 years with complete traceability through Quipsite.
Global delivery to investigator sites with real-time tracking. We handle customs, import requirements, and last-mile delivery.
Real-time visibility of equipment operations, complete traceability, and audit-ready documentation throughout your study.
Dedicated support throughout your trial — troubleshooting, replacement devices, on-site assistance. Response within 24h.
Certifications
All devices we supply are approved by the relevant regulatory bodies in the countries of use.
Compliance with Regulation (EU) 2017/745 (MDR) and, where applicable, Regulation (EU) 2017/746 (IVDR).
Compliance with applicable U.S. FDA medical device requirements, including 510(k) clearance, De Novo classification, or PMA approval, as applicable.
Compliance with the UK Medical Devices Regulations 2002 (SI 2002 No. 618, as amended).
Compliance with Canada's Medical Devices Regulations (SOR/98-282), including applicable MDL or MDEL requirements.
Compliance with Japan's Pharmaceuticals and Medical Devices Act (PMD Act).
Contact
Our team sources any laboratory equipment globally — even if it's not in our catalog. Tell us what your protocol requires and we'll find it. Response within 24 hours.
Easy there — at Quipment, every shipment is handled with care.