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DocumentMS

Industries

Dokumentenmanagement nach Branche

Retention periods, naming conventions and approval chains differ by sector, and a generic configuration satisfies none of them. Each page below names the regulations that apply in that industry, gives a starting folder taxonomy, a worked approval workflow and the retention periods commonly required.

What changes between one sector and the next

Four things, and only four. Everything else is the same platform.
  • The taxonomy

    Whether documents are organised by matter, asset, consignment, batch or record class. This is the decision that is hardest to change later.

  • Mandatory metadata

    Which fields cannot be left blank — consignment reference, matter number, batch number, asset reference — because they are what makes retrieval possible.

  • Approval thresholds

    Who must approve what, and at what value or risk level a second approver is added.

  • The retention trigger

    What event starts the clock. Creation, closure, expiry, end of production, end of relationship, or the subject reaching the age of majority.

At a glance

The driving regulation and retention trigger by sector

The two settings that most determine a configuration, side by side. Each row links to the full page for that sector.
Primary regulatory driver and retention trigger by industry
IndustryPrimary regulatory driverWhat starts the retention clock
HealthcareHIPAA Security Rule — technical safeguards (45 CFR §164.312)Later of creation date or the date it was last in effect
Financial servicesSEC Rule 17a-4 (Exchange Act records preservation)Creation, or the end of the fiscal year in some cases
LegalDuty of confidentiality and legal professional privilegeMatter closure
Pharma & life sciencesFDA 21 CFR Part 11 (electronic records; electronic signatures)Batch expiry or QP certification
GovernmentFreedom of information and public records accessNot applicable — permanent preservation
Construction & engineeringISO 19650 information managementPractical completion or final certificate
ManufacturingISO 9001:2015 control of documented information (clause 7.5)End of production and service for the part
Energy & utilitiesSafety case and permit-to-work regimesDecommissioning
LogisticsCustoms recordkeeping obligationsEnd of the year in which the declaration was accepted
EducationStudent record access rights — FERPA (US) and UK GDPR / GDPRSubject reaching the age of majority

The regulations and retention periods referenced across these pages are starting points drawn from the common position in each sector. Confirm them against the territories and registrations you actually operate under before you rely on them — nothing on this site is legal advice.

Configurations

Ten industry configurations

Each page names the regulations that apply, maps five capabilities to them, and gives a starting taxonomy, a worked workflow and a retention table.
  • Healthcare document management

    Healthcare organisations hold two very different kinds of document, and conflating them is the root of most compliance problems. Clinical records about identifiable patients carry the heaviest obligations: recorded access, minimum-necessary disclosure and retention periods set by state law rather than by federal rule.

    Read the healthcare configuration
  • Financial services document management

    Financial services is the sector where document requirements are written as rules rather than principles. Most industries decide their own retention periods from a risk assessment; broker-dealers, investment advisers and banks are told what to keep, for how long, in what format, and how quickly they must produce it.

    Read the financial services configuration
  • Legal document management

    Legal document management is organised around the matter, not the author or the department. That single structural difference drives everything else: permissions follow matter teams, retention follows matter closure, conflicts checks operate on matter membership, and a document’s meaning is inseparable from the matter it belongs to.

    Read the legal configuration
  • Pharma & life sciences document management

    Life sciences is the sector with the strictest electronic records requirements of any we work with, and the one where a document system itself becomes an object of inspection. Under FDA 21 CFR Part 11 and EU GMP Annex 11, the system holding your batch records is not neutral infrastructure — it must be validated, its audit trail must be computer-generated and unalterable, and its electronic signatures must be provably linked to the records they apply to..

    Read the pharma & life sciences configuration
  • Government document management

    Public sector document management is dominated by two obligations that pull in opposite directions. Disclosure law requires you to find and release records to anyone who asks, within a statutory deadline.

    Read the government configuration
  • Construction & engineering document management

    Construction document management is a revision-control problem before it is anything else. Work built to a superseded drawing is the single most expensive documentation failure available on a site, and it happens through an entirely mundane sequence: a revision is issued, someone is working from a printout, and nothing in the process makes the difference visible.

    Read the construction & engineering configuration
  • Manufacturing document management

    Manufacturing document management turns on a single question that an auditor will ask in some form on every visit: was the document the operator used the current approved one? Everything else — change control, training records, supplier documentation — exists to make the answer to that question reliably yes. A repository that stores documents well but cannot evidence which revision was in use on a given shift has not solved the problem..

    Read the manufacturing configuration
  • Energy & utilities document management

    Energy and utilities document management follows the asset, and the asset outlives everything around it — the project that built it, the contractor that commissioned it, the software that documented it, and usually the people who understood it. A substation or a pipeline commissioned in the 1980s is still operating, and the commissioning records still matter when it is modified.

    Read the energy & utilities configuration
  • Logistics document management

    Logistics document management is a capture problem before it is a storage problem. The documents that decide whether a claim succeeds — a signed delivery note, a damage photograph, a temperature log, a customs declaration — are produced away from any office, by drivers and warehouse staff, on a phone, often in poor conditions.

    Read the logistics configuration
  • Education document management

    Education document management has to accommodate record types whose sensitivities differ by an order of magnitude, held by one institution and often in one system. An enrolment form, a safeguarding referral, a staff disciplinary file and an accreditation evidence pack all need different permissions, different retention periods and different disclosure treatment.

    Read the education configuration

FAQ

Questions about industry configurations

Sector-specific questions are answered on each industry page.
How much does an industry configuration actually differ?

The modules are the same; the configuration is not. What differs is the folder taxonomy, which metadata fields are mandatory, where the approval thresholds sit, and — most consequentially — what event starts each retention clock. A healthcare configuration and a logistics one share every feature and almost no settings.

What if our sector is not listed?

The ten here are where we have the most implementation experience, not the limit of what the product suits. The useful question is which of these your document population most resembles: heavily regulated with recorded-access duties, asset-centred with decades-long retention, or high-volume with short-lived evidential records.

Are the retention periods on these pages usable as a schedule?

No, and each page says so explicitly. They are starting points for a conversation with your counsel or records manager. Retention varies by jurisdiction, entity type and circumstance, is extended for minors in several sectors, and is displaced entirely by a legal hold.

Which industries have the strictest document requirements?

Pharmaceuticals and life sciences, by a clear margin — 21 CFR Part 11 and EU GMP Annex 11 require a validated system with a computer-generated, unalterable audit trail retained at least as long as the records. Financial services is next, because SEC Rule 17a-4 constrains the storage medium itself.

Can one tenant serve several sectors?

Yes. Retention rules attach per record class rather than per tenant, and branch separation keeps entities apart under central administration. A group operating a manufacturing arm and a logistics arm applies different taxonomies and periods in the same system.

Eine 30-minütige Sitzung mit einem Solutions Engineer, mit einer Ordnerstruktur und Freigabekette, die Ihren ähneln — kein allgemeiner Demo-Mandant.