Let's set up your first project.

Lucora RM works on projects — usually one project per product or program. Pick the starting point that matches what you have.

Whichever you pick, nothing is permanent. You can change the artifact types, prefix scheme, and review workflow any time from project settings.

Pick a template

Each template configures your artifact types, ID prefix scheme, default review scope, and (optionally) seeds a starter set of common items so you have something to react to.

None of these match? Pick "Generic V-model" — you can rename, add, or remove artifact types in Step 3.

Project details

Name and identify your project. The slug becomes part of every shareable URL.

Project name

Shown in the project switcher and exports.

URL slug

rm.lucora.app/acme-biotech/

Letters, numbers, hyphens. Cannot be changed after items are committed.

Description (optional)

Review workflow

How items move from draft to approved

Artifact-level

Each item moves through draft → review → approved independently.

Document-level

Approve a baseline as a unit; items inherit the baseline's state.

Hybrid recommended

Artifact-level for daily work; document-level snapshots for formal releases. What most regulated teams actually do.

Artifact types & ID prefixes

Pre-filled from your template. Edit any cell to customize.

Type	Label	Prefix	Padding
UN	User Need	UN-	4
SR	System Requirement	SR-	4
SS	Software Requirement	SS-	4
DS	Design Spec	DS-	4
UT	Unit Test	UT-	4
IT	Integration Test	IT-	4
VT	Verification	VT-	4
VAL	Validation	VAL-	4

Compliance & defaults

Sensible defaults from your template; toggle to taste

Capture status events for audit

Required for Part 11–ready exports. On by default.

Require admin approval to change status

Most regulated workflows want this on.

Default landing view

First-time users land here when they open the project.

Ready to create your project

Quick recap. You can change everything later from project settings.

Artifact types

8

Starter items

14

Review scope

Hybrid

Audit log

On

Settings summary

Project	CGM-v2 · acme-biotech / cgm-v2
Template	FDA-class medical device (21 CFR 820 / IEC 62304)
Review workflow	Hybrid — artifact-level day-to-day, document-level for releases
ID prefix scheme	UN- / SR- / SS- / DS- / UT- / IT- / VT- / VAL- (4-digit padding)
Status events captured	Yes (Part 11–ready)
Default landing view	Table
Starter items	14 example items pre-loaded so you have something to look at

After creation, the next thing you'll see is a guided tour highlighting the table view, graph view, and import button. You can dismiss it any time.