| Beyond the Upgrade: What to Consider Before Migrating to STARLIMS v12.x  Modernizing a legacy LIMS with STARLIMS v12.x helps laboratories reduce technical debt, improve system maintainability, and streamline workflows. Strategic migration planning, risk-based validation, and cross-functional governance support lower long-term costs and sustainable laboratory operations.[Read More]
Does Your LIMS Need to Be Validated? What Each Regulator Asks For  LIMS validation remains the laboratory’s responsibility, not the software vendor’s. Regulated laboratories must validate their systems for intended use, including configurations and workflows. Risk-based approaches support compliance with Part 11, Annex 11, and ISO 17025, while ongoing change control maintains validation throughout the system’s lifecycle.[Read More]
From Data Capture to Decision: Why EDC Should Drive Your Clinical Oversight Operating Model  ICH E6(R3) raises expectations for risk-based clinical trial oversight. Integrating EDC data quality signals with CTMS oversight decisions helps sponsors and CROs close accountability gaps, document corrective actions, and demonstrate how emerging trial risks are identified and resolved.[Read More]
CSols Inc.: We’re recruiting for a LabVantage BA - Remote USA  CSols, Inc., is seeking a talented LabVantage LIMS Consultant to join our team and deliver high quality laboratory informatics solutions to our clients. If you enjoy working at the intersection of science and technology, and thrive in client-facing roles, we want to hear from you. Experience in the gene therapy space is a plus![Read More]
From Legacy Workflows to Paperless Labs: Track Every Sample, Process, and Decision  See how connected laboratory workflows can bring greater control and visibility to sample tracking, data capture, and traceability. This on-demand webinar uses a real-world example to show how paperless processes can streamline lab operations while supporting compliance requirements.[Read More]
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