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Reynolds delivers retention 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.
Long-term retention of executed batch records, validation files, and quality archives, using product- and study-specific schedules with an audit trail.
TMF retention, study binder archives, and CRF retention — FDA / EMA inspection-ready disposition workflow.
SOPs, training records, deviations, CAPAs — retention enforced with Part 11 e-signatures and audit trail.
Submission packages, regulatory correspondence, and audit evidence — version-controlled long-term retention.
Retention schedules, lifecycle policies, legal hold, and disposition workflows for regulated records programs.
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 retention.
A buyer's guide to OpenText ApplicationXtender (now AppEnhancer) for IT and records evaluators: what it is, its path from Documentum to OpenText, how it works, its versions and end-of-support timeline, ECM market context, document-management ROI, how it compares to the alternatives, and how to plan a migration.
A neutral, fully cited comparison of Iron Mountain and the alternatives for Pennsylvania records management — the recurring-rent model, the contract clauses that create lock-in, the economics of digitize-then-destroy, and how to decide whether to switch.
How Pennsylvania organizations evaluate alternatives to Access Information Management: the real economics of off-site box storage, the retrieval and exit fees that rarely appear in a quote, when to digitize instead, and the PHMC and County Records Act rules that govern retention and lawful destruction.
Get our life-sciences retention playbook — Part 11 e-records configuration, GMP retention schedules, and TMF retention guidance.
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.