NPI & TECHNOLOGY TRANSFER

NPI & Technology Transfer

We transfer design outputs into production-ready processes and records, then assess readiness for pilot execution.

RECOMMENDED FORLab-on-a-chip teams moving from engineering prototypes to a repeatable production state

Scope of work

Before contracting, we confirm the current state and responsibility boundary, then fix only the necessary work in scope.

01

Receive product requirements, drawings, BOMs, and prototypes

02

Review manufacturability, CTQs, process windows, and inspectability

03

Assess materials, outsourced processes, and supplier readiness

04

Define gap actions and approval criteria before the pilot lot

Evidence that remains

We prioritize the connection between requirements, execution, results, and approval over document names.

01Technology transfer checklist
02Process flow and draft work instructions
03CTQ and inspection criteria
04Pilot readiness report

Workflow

We review each stage before moving forward and retain unresolved items in a controlled action register.

  1. 01

    Receive outputs

    Confirm design authority, transfer scope, and current revisions.

  2. 02

    Review gaps and risks

    Assess manufacturability and inspection feasibility from process and quality perspectives.

  3. 03

    Standardize

    Convert material, process, inspection, and record requirements into controlled execution documents.

  4. 04

    Decide readiness

    Close or condition unresolved items before pilot execution.

Conditions and responsibility boundary

Product architecture and core design authority remain with the NRE and design specialist. Trova Health owns manufacturing execution, records, and quality operations after transfer.

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