Chemistry Testing

3 weeks ago

Dublin, Dublin City, Ireland Tentamus Group Full time

We detect and identify visible and sub-visible particles in pharmaceutical products to ensure patient safety and product integrity.

Advanced analytical techniques such as FTIR and LC-MS are used to identify unknown substances and verify formulation components.

We perform precise quantitative analysis of active pharmaceutical ingredients (API) to confirm label claims and batch consistency.

Comprehensive impurity analysis to monitor degradation products and related compounds in line with ICH guidelines.

Gas chromatography-based methods for identifying and quantifying residual solvents as per ICH Q3C requirements.

From pH and osmolality to particle size and melting point — we analyse critical physical properties to support formulation stability and performance.

Method development and testing for dissolution and drug release profiles across immediate, delayed, and extended-release formulations.

Full compendial and non-compendial testing to qualify pharmaceutical excipients and APIs prior to use in manufacturing.

Long-term and accelerated stability testing under ICH conditions to support shelf-life, packaging, and formulation decisions.

Customised analytical method development and ICH-compliant validation services for drug substance and drug product testing.

Qualified release testing in accordance with EU GMP requirements, supporting timely product release to the market.

  • MHRA and GMP-compliant laboratory
  • Fast turnaround times & flexible scheduling
  • Schedule 1-4 Controlled Drugs License
  • Experienced team of pharmaceutical chemists
  • State-of-the-art analytical instrumentation
  • Fully traceable, audit-ready data

Looking for a trusted partner for pharmaceutical chemistry services? Leave us a message through our contact form and we will help you meet your quality and regulatory goals.

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