PHARMACEUTICAL APPLICATION

Biopharmaceutical Aseptic Sampling System Solution

Build multi-point or multi-bottle aseptic sampling paths with single-use sampling manifolds, closed-container closures, TPE tubing, and vent filters to reduce cross-contamination.

PROCESS CHALLENGES

Key process considerations

  • Repeated sampling must keep the main process and unused sample containers closed
  • Sample volume, purge volume, and residual hold-up can affect sample representativeness
  • Sample bottles, vent filters, heat-seal locations, and operating sequence must match the site process

SELECTION WORKFLOW

From process to configuration

Confirm the operating envelope and compatibility of the complete fluid path.

01

Sampling plan

Confirm sampling points, frequency, volume per sample, bottle count, purge volume, and downstream sample testing.

02

Fluid-path configuration

Select main-line and branch sizes, sample containers, closures, vent filters, and pinch-clamp locations.

03

Aseptic operation

Confirm connection, sampling, heat-seal disconnection, labeling, packaging, and pre-sterilization requirements.

MATCHED PRODUCTS

Products for aseptic process sampling

A starting point for selection. Confirm each specification against the actual process and validation requirements.

Send process details →

FAQ

Frequently asked questions

How many sample bottles can a single-use sampling manifold support?

The bottle count can follow a standard product configuration or project requirement. Confirm it against the sampling frequency, volume, main-line size, and available operating space.

How can cross-contamination risk during sampling be reduced?

Use a pre-assembled, pre-sterilized fluid path, closed sample containers, independent branches, and heat-seal disconnection, supported by a clear operating sequence.