Cosmetic batch and release documentation must align with GMP ISO 22716 procedures, production controls and quality checks. Biolevate assists review by flagging missing information, inconsistencies and source-linked issues.
Faster GMP documentation QC
Accelerate first-pass review of cosmetic batch and release documentation against GMP ISO 22716 procedures, production records and quality controls.
Earlier documentation issue detection
Flag missing entries, signature gaps, formula inconsistencies, out-of-spec checks and incomplete release evidence before final QA review.
Audit-ready GMP traceability
Link each issue and reviewer decision to the relevant batch record, SOP, specification, GMP requirement or release criterion.
How it works
1
Ingest GMP records — collect batch records, production logs, specifications, SOPs, release forms and ISO 22716 procedures.
2
Map review criteria — define required checks, signatures, specifications, formula constraints and release criteria.
3
Run documentation QC — detect missing fields, inconsistencies, deviations and incomplete quality evidence.
4
Produce the QC run record — generate an issue log with source links, reviewer decisions and remediation notes.
ISO 22716 review logic: check cosmetic batch and quality records against GMP controls, production steps and release documentation requirements.
Source-linked issue log: every detected gap, deviation and decision is captured for audit readiness and QA follow-up.