Annex 07 — Documentation & Evidence Standards
07.1 Purpose
This annex defines the standardized documentation and evidence requirements for all VILF-compliant labs, hubs, and the Network Coordination Unit (NCU).
It ensures documentation integrity, auditability, transparency, and interoperability across the innovation ecosystem.
07.2 Evidence Principles
All evidence must be:
- Complete — all IMM-P® stages must include required artifacts
- Traceable — decisions, changes, and iterations must be recorded
- Versioned — repository retains chronological history
- Auditable — evidence must support MEL and accreditation
- Accessible — clearly named, properly stored, searchable
07.3 Evidence Repository Structure
Standard folder hierarchy:
/evidence /00-pre-discovery /01-discovery /02-validation /03-efficiency /04-scaling /05-continuous-improvement /governance /risks /prototypes /experiments /maturity /mel
07.4 Metadata Requirements
Every file must include a metadata header:
- Title
- Author
- Date
- IMM-P® Stage
- Version
- Evidence Type
- Related Decision Record(s)
- Tags
07.5 Decision Record Format
All decisions must be logged using the following fields:
- Decision title
- Context
- Evidence used
- Options considered
- Final decision
- Responsible person
- Date
- Escalation status
- Link(s) to related evidence
07.6 Prototyping & Experimentation Logs
Prototyping Log (Minimum Fields)
- Prototype version
- Objective
- Features tested
- Feedback received
- Iteration notes
Experiment Log (Minimum Fields)
- Hypothesis
- Method
- User group
- Results
- Interpretation
- Next steps
07.7 Repository Hygiene Rules
- No duplicate files
- No orphan evidence (all files must map to a stage)
- No undocumented decisions
- No “final_v2_final_really_final” filenames
- Version numbering:
v1,v1.1,v2, etc. - Annual evidence consolidation required
07.8 Licensing
All repository structures and templates are released under CC BY-NC-ND 4.0.