Equipment Certifications

Indock supplies supplement manufacturing equipment that is CE-marked and built to GMP-compliant standards, with documentation aligned to ISO, HACCP, and RoHS, plus IQ/OQ/PQ validation templates to support your qualification. The aim is equipment that fits straight into a regulated supplement or nutraceutical facility with the paperwork your auditors expect.

The standards that matter

• CE marking: confirms the equipment meets the applicable EU health, safety, and environmental requirements.
• GMP-compliant build: equipment designed for Good Manufacturing Practice production environments.
• ISO, HACCP, RoHS: documentation aligned to recognised quality, food-safety, and hazardous-substance expectations.

Validation: IQ, OQ, PQ

Validation templates help your team document that the equipment was installed correctly (IQ), operates across its intended range (OQ), and performs consistently with your product (PQ). Completed records support your qualification and your GMP audits.

What stays with you

CE and validation documentation supports your compliance, but site-level GMP certification and EU food-supplement regulatory compliance remain your facility’s responsibility. We provide the equipment-side documentation to make that work easier.

You receive CE documentation in the proposal stage, before purchase. For the on-site side of go-live, see installation and commissioning, or request a quote for your product and volume.

Frequently asked questions

What certifications does the equipment carry?

What are IQ, OQ, and PQ?

Will the documentation support my GMP audit?