How does SLP ensure quality and compliance?
Quality and compliance in medical kitting are not achieved through inspection alone — they are built into every process, from component sourcing through kit assembly to outbound shipment. Strategic Lab Partners operates a documented quality management system that integrates with SLP CONNECT to enforce lot control, expiration management, and assembly verification at every production step, creating a chain of custody that withstands regulatory scrutiny.
Typical quality and compliance measures include:
Practical applications:
- Verifying component lot numbers and expiration dates against program specifications before kit assembly begins.
- Applying documented assembly checklists and in-process QC checks at defined production milestones.
- Quarantining non-conforming components and kits and initiating CAPA processes through SLP CONNECT.
- Maintaining complete batch records linking every finished kit to its component lots and assembly personnel.
- Providing clients with on-demand QC documentation and audit support through SLP CONNECT reporting.
- Documented procedures: written processes for assembly, inspection, and handling.
- Controlled materials: approved components and packaging with defined specifications.
- Inspection and sign‑off: checks at key points in the process, with accountability.
- Traceability: lot, batch, or order‑level tracking where required.
- Exception handling: clear paths for managing non‑conforming product or changes.
What this prevents: delays, loss without defensible history, inventory gaps, and after-the-fact reconciliation.
For healthcare, clinical, and regulated programs, we work with your quality and regulatory teams to ensure that our kitting and 3PL operations align with your internal standards and external obligations.
If your program is decentralized or regulated and you're experiencing avoidable disruption, SLP can help you map failure points and implement a more governable approach.
Contact SLP →