Industry challenges
- Control upgrades on equipment operating under validated processes
- Documentation and traceability of changes
- Obsolete controls on qualified equipment
- High accuracy and repeatability in dosing and packaging
Automation where change must be controlled
In pharmaceutical manufacturing, a control modification is also a quality event. NSPL plans upgrades so that functional specifications, test protocols and as-built documentation support the customer’s change-control process.
Related: Retrofit & Modernization, Commissioning.
Applications
- Blister packaging and cartoning
- Liquid and powder filling
- Labelling and serialisation stations
- Inspection and reject handling
Partner products
Products from NSPL’s principal partners that are commonly used here.
Frequently asked questions
Can NSPL support machine-control upgrades in regulated manufacturing environments?
NSPL can plan and execute control upgrades with the documentation, test records and change descriptions that regulated manufacturers need for their own change-control and validation processes. Responsibility for qualification and validation remains with the manufacturer's quality organisation.