Operators in cleanroom coveralls in a pharmaceutical production area

Pharmaceuticals & Biotech

Hygienic process equipment and documented spares for regulated production.

20 / 21Sector

In pharmaceutical production a spare part is also a compliance question: the surface finish, the elastomer grade and the certificate all matter. We supply hygienic process components and utilities spares with documentation that stands up to an audit.

Diaphragm valves, sanitary pumps, tri-clamp fittings and tubing, sterile filters and housings, single-use components, clean-utility instrumentation, and spares for autoclaves, lyophilisers, isolators and filling lines.

Product-contact parts are supplied with material certificates, surface-finish records and elastomer conformity statements: FDA, USP Class VI or EC 1935/2004, as the application requires.

Typical supply

What we are asked for most

  1. 01Aseptic diaphragm valves and actuators
  2. 02Sanitary centrifugal and lobe pumps
  3. 03Tri-clamp fittings, tubing and gaskets
  4. 04Sterile filter cartridges and housings
  5. 05Clean-steam traps, regulators and sample valves
  6. 06Conductivity, TOC and pressure instrumentation
  7. 07Autoclave, lyophiliser and filling-line spares
  8. 08Cleanroom HVAC filters and consumables

What matters here

Three things this sector does not forgive

  • 01 / 03

    Documentation

    Material, surface-finish and elastomer certificates are supplied per item and per batch.

  • 02 / 03

    Like for like

    Validated equipment gets the exact specified part. Substitutions are never made without written approval.

  • 03 / 03

    Cleanliness

    Hygienic components are capped, bagged and labelled to stay clean through to installation.

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