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V5 Sample Labeling & LIMS Scheduling

Identify. Test. Approve.

October 3, 2025

7 min read

Articles, Life Sciences, QMS

Ensure your validated 21 CFR Part 11 software doesn’t sidestep predicate GMP requirements. Learn why dual-control (4‑Eyes) checks remain mandatory for compliance.

Double‑Check: 4‑Eyes Oversight in Part 11 Software Governance

Software Needs Oversight

July 16, 2025

4 min read

Articles, Dietary Supplements, Pharmaceutical

Diagram comparing electronic batch records (eBR) with traditional batch manufacturing records for GMP compliance

Electronic Batch Record Software

Paperless Record Integrity

July 7, 2025

4 min read

Diagram comparing electronic batch records (eBR) with traditional batch manufacturing records for GMP compliance

Electronic Batch Record Systems

Paperless Record Integrity

July 7, 2025

3 min read

Diagram comparing electronic batch records (eBR) with traditional batch manufacturing records for GMP compliance

Electronic Batch Record Pharma (eBR)

Paperless Record Integrity

July 7, 2025

3 min read

Diagram comparing electronic batch records (eBR) with traditional batch manufacturing records for GMP compliance

Electronic Batch Record (eBR)

Paperless Record Integrity

July 7, 2025

5 min read