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Reynolds delivers ecm solutions purpose-built for life sciences — backed by 55+ years of regulated-industry experience and 100% client retention.
These are day-to-day workflows Reynolds can configure for life sciences organizations.
SOPs, training records, deviations, CAPAs, change control — all managed with Part 11 electronic signatures and audit trail.
Electronic batch records with validation status, lot release workflow, and lot traceability — supports FDA / EMA inspection.
Trial master file (TMF) organization, study protocols, case report form management — GCP-aligned access controls.
Submission package assembly, version control, structured export, and regulatory correspondence tracking.
Laserfiche-powered ECM with workflow automation, retention scheduling, and integrations.
Founded in 1970, Reynolds supports life sciences organizations with FDA 21 CFR Part 11 and cGMP-aligned records and cleanroom storage, serving clients including Biocoat and Air Products.
Electronic records & signatures
Current Good Manufacturing Practice
Practical guides from the Reynolds Resource Hub on ecm.
A buyer's guide to Laserfiche for government, healthcare, finance, and education evaluators: ECM and records management, product areas, cloud versus on-premises deployment, workflow business cases, current DoD records requirements, pricing factors, alternatives, and a defensible evaluation process.
How to implement Laserfiche as a phased records project — scoping record types and retention, back-file digitization, folder and metadata design, security and records configuration, phased rollout, change management, and the pitfalls that derail go-live.
SharePoint ships with every Microsoft 365 subscription, but records management is a separate Purview compliance layer, not a native SharePoint feature. A cited comparison for Pennsylvania county and township records offices deciding between the two.
Get our life-sciences Laserfiche playbook — Part 11 validation checklist, eQMS workflow templates, and TMF structure recommendations.
Review the practical reference and contact Reynolds with questions.
The Reynolds team will review your life sciences requirements and follow up about the appropriate next step.