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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 the day-to-day workflows where Reynolds delivers measurable improvement for life sciences organizations.
Long-term retention of executed batch records, validation files, and quality archives — typical 15+ year retention with 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.
Reynolds has delivered FDA 21 CFR Part 11 and cGMP-aligned records and cleanroom storage for life sciences organizations since 1970, serving clients including Biocoat and Air Products.
Electronic records & signatures
Good Manufacturing Practice
Good clinical/laboratory 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.
No sales pitch — just the practical reference.
Same-day response. No bots, no call centers — you'll talk to one of our life sciences-experienced specialists.
