At KamTek, quality isn't just a process—it's our culture.
Every sample entrusted to us is handled by trained professionals who understand their value and is monitored under a rigorously validated Quality Management System (QMS) grounded in ISO 9001:2015 principles and global best practices.
From sample storage to processing, distribution and clinical research support, we treat every sample with care that it deserves —because we believe that behind every vial is a patient, perhaps a breakthrough, a cure in waiting.
KamTek’s Quality Management System (QMS) guides our operations across biorepository management, laboratory services, logistics, and IT infrastructure. Our quality systems are structured around:
KamTek is powered by trained experts:
KamTek ensures zero downtime for biospecimen safety.
Power Continuity:
Environmental Redundancy:
Storage unit Backups:
KamTek has a proven disaster preparedness plan tested in real emergencies (e.g. Hurricane Sandy). We activate full checklists during weather alerts:
Backup systems support all cryo-storage, communications, and monitoring functions even during power or internet outages. Every scenario is covered, every second counts.
Access Control:
Surveillance:
Emergency Alerts:
Every door is logged, every visitor signed in, and every motion tracked. Security simulations are conducted monthly, and only authorized personnel are permitted near samples and sensitive systems.
KamTek’s digital security strategy safeguards both data and operations:
Network &Data:
KamTek’s commitment to regulatory compliance, operational excellence, and quality assurance is regularly validated through audits conducted by government agencies, commercial partners, and industry leaders.
These external third-party assessments reinforce our position as a trusted service provider in the biotech and research community.
Verification of storage integrity and freezer performance for pharmaceutical samples.
Audit of cryogenic storage protocols for long-term specimen preservation.
Assessment of KamTek’s compliance and laboratory infrastructure
Verified secure handling and documentation procedures for sensitive legal specimens
Audit on KamTek’s technical operations, SOPs, and facility protocols.
Evaluation of laboratory and biorepository operations for GMP alignment
Audit on KamTek’s technical operations, GMP Storage, SOPs, and facility protocols.
Assessment of compliance and capabilities for federally funded bio preservation programs.
Comprehensive quality system review for ISO certification readiness
KamTek isn’t just compliant. We are committed, qualified, and disaster tested. When your research depends on the safety of a sample, the stability of a system, or the reliability of a partner, KamTek delivers.