

CDMO ERP Selection - 12 Must-Have Capabilities for 2026
Based on our life sciences experience supporting outsourced operators, including contract development and manufacturing organizations (CDMO) and contract research organizations (CRO), this guide summarizes the ERP software selection requirements vendors must prove, demo, and document.
Dec 1, 20257 min read


Life Sciences ERP Software Selection - 2026 Buyer’s Guide for Validated (GxP-Ready) Environments
Choosing ERP in a validated environment is different. This 2026 buyer’s guide shows how to evaluate life sciences ERP through a GxP lens—Part 11 e‑signatures, audit trails, QA release, lot/expiry traceability, and LIMS/QMS/EDMS integrations. Get selection criteria, a weighted scorecard, and five scripted demos to run with your data so your shortlist is CSV‑ready before contracts.
Nov 20, 20257 min read


How to Accomplish FDA Validation for ERP Software
Validation is proving that a system meets the intended purpose it was designed for by confirming that the system works properly. Validating an ERP system involves testing and validating its various components, including security controls, configuration settings, processes, functions, and reports.
Jan 25, 20236 min read







