KamTek provides disposal services for a wide range of research and clinical materials. Every disposal includes a certificate of destruction, ensuring full traceability and compliance documentation.

Destroyed using validated autoclaving or degradation protocols.

Shredded securely using industrial-grade, high-performance shredders.

Removed and neutralized by certified third-party vendors following validated procedures.
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Decontaminated in-house or disposed through validated hazardous waste vendors or surplused in house if in good working condition.

Consulted and cleared with local authorities, EPA, or equivalent regulatory bodies.
Initiated via KamTek’s Sample Destruction Request Form outlining the items, volume, and disposal method.

A digital workflow is created in KamTek’s eQMS software for this request, timestamping every step and ensuring full accountability.

Samples are carefully withdrawn from their storage locations using validated 'specimen withdrawal containers' maintained at the optimal temperature required for the samples (RT/4oC/-20oC/-80oC/LN2).

Materials are destroyed using approved methods—autoclaving, shredding, decontamination, or vendor disposal—based on item type and regulatory requirements.

A detailed Certificate of Destruction is generated and sent to the client along with a summary report, meeting internal and external audit requirements.

We follow local, state, federal, and international guidelines, including consultation with EPA and equivalent authorities.
All destruction methods are tested, documented, and traceable—including SOPs, vendor validations, and equipment logs.
From sample receipt, storage, processing, analysis and disposal, we handle it all—reducing the operational burden on your team.
Every step, from sample retrieval to certificate generation, is tracked and audited.
Biotech, pharma, academic, and government clients rely on KamTek for safe, compliant disposal solutions.
KamTek can assemble clinical trial collection kits, diagnostic or test kits, research reagent kits, biological sample kits, tissue slide kits, and custom drug shipment kits. Each kit can be tailored to the study protocol, product workflow, or client-specific SOP.
Yes. KamTek can work with your team to design a kit based on your protocol, collection requirements, storage conditions, shipping needs, and documentation requirements. We can support both sterile and non-sterile kit configurations depending on the project scope.
Yes. KamTek can assist with component sourcing and procurement, including tubes, vials, swabs, labels, bags, boxes, return materials, reagents, instructions, forms, and other approved supplies. Received components are inspected, documented, and tracked before use in assembly.
Yes. KamTek can support blinded labeling, sponsor-specific naming conventions, study IDs, visit numbers, site IDs, patient-facing labels, and other protocol-defined identifiers. Labeling workflows are reviewed before production to reduce the risk of kit assembly or distribution errors.
Yes. KamTek has four inhouse labs where sample aliquoting, reagent preparation, and other lab based activities can be performed. We are flexible in your project requirements and a project specific SOP is prepared and implemented once signed and approved by the client. A version change will be initiated if there is a change in the protocol.
KamTek performs QC checks before and during the kitting process and before shipment. These checks will include verification of component type, quantity, label accuracy, lot number, expiration date, documentation, packaging condition, and final kit completeness. The QC actions will be documented.
Yes. KamTek can track component lot numbers, expiration dates, batch information, and kit build records. This helps support controlled release, recall readiness, replenishment planning, and client reporting.
Yes. KamTek can store completed kits or kit components at appropriate controlled temperatures, including room temperature, refrigerated, frozen, ultra-low, and liquid nitrogen conditions when required by the project.
Yes. KamTek can support domestic and international kit distribution, including multi-site shipping, expedited courier options, validated packaging, cold chain logistics, tracking, and shipment notifications.
Yes. KamTek can support refill and reorder programs for long-term studies, recurring R&D workflows, and ongoing clinical or diagnostic programs. Inventory levels can be monitored so kits and components are replenished before shortages occur.
KamTek makes compliant disposal simple. Whether it’s a one-time cleanout or ongoing need, we provide secure, certified destruction with full documentation—start to finish.