LYZE LABS™Controlled document
LZ-SOP-QC-01Revision 4

Batch Acceptance and Release

How a batch is judged and who decides. A batch is released only when every determination on its certificate sits inside the specification set for that compound before the sample was run.

Document control

Document referenceLZ-SOP-QC-01
Revision4
Effective fromOctober 31, 2025
Next review dueOctober 28, 2026
Document ownerQuality Control
CoversEvery lot tested; release decision

Provisions

  1. Each compound has a written specification, agreed before any batch is analysed against it
  2. Every batch is sampled and analysed on arrival; verification is per batch, never inherited from a previous lot
  3. Release requires every determination inside specification, with no exceptions granted at the bench
  4. Independent third-party confirmation is obtained before release, and published alongside our own result
  5. The release decision and the analyst who made it are recorded against the lot
Scope. This document forms part of the Lyze Labs quality system and applies to research reference material supplied for in vitro laboratory use. It is not a marketing authorisation, a regulatory approval, or a claim that material may be used in humans.

Document control. LZ-SOP-QC-01 is an internal controlled document reference in the Lyze Labs namespace. It is not an accreditation or certification number issued by an external body. A superseded revision is archived rather than destroyed, so what was in force on any given date can be established.

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