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Pharmaceutical Testing

Analytical rigour for materials and finished products.

01 Overview

Analytical rigour from raw material to release.

Support across raw material qualification, in-process control, release testing and stability programmes, with method development and validation where an existing method will not carry the work.

02 Testing capabilities
01

Assay and Purity

Quantitative determination of actives against the applicable monograph or specification.

02

Impurity Profiling

Identification and quantification of related substances and degradants.

03

Stability Studies

Storage condition programmes supporting shelf-life and packaging decisions.

04

Microbiological Testing

Bioburden, sterility support and specified organism testing.

05

Method Development & Validation

New methods, transfers and validation to demonstrate performance.

Industries served

Testing is scoped to the sector, the destination market and the claim being supported.

  • Pharmaceuticals
  • Nutraceuticals
  • Healthcare
  • Excipient suppliers
  • Contract manufacturers
  • Exporters
03 Why SOS
01

Quality support

Incoming material control, in-process checks and release testing under one technical relationship.

02

Compliance assistance

Documentation, data interpretation and the technical review your quality team needs.

03

Excipient sourcing

Pharmaceutical excipients available through our raw material vertical.

04 Let's talk

Have a scientific challenge? Let's solve it.

  • Testing requirement?
  • Ingredient requirement?
  • New product?
  • Compliance question?
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