Our onsite Quality control laboratory is committed to maintaining high standards in today’s competitive pharmaceutical industry. Quality is essential for our products to stand out in the pharmaceutical sector, and we ensure this through compliance with GMP guidelines, using a broad range of qualified analytical equipment, SOPs and validated test methods.

Our laboratory is staffed by experienced experts.  Due to the diversity of the expertise, we are not only able to analyse finished medicinal products to meet stringent quality standards, but we are also able to develop and validate methods in-house. 

We have capability to conduct ICH-compliant stability studies under various conditions, including accelerated, real-time, and cold storage. These studies help us to ensure optimal shelf life for our products and the detailed analyses to provide the necessary data to support our regulatory submissions.  

The analytical techniques available include HPLC-UV, GC-FID, GC-MS, UV-Vis, IC, FTIR, dissolution, auto-titration, viscosity, density, pH and other general techniques.

Our QC lab supports Northumbria Pharma’s mission to provide innovative products at the heart of patient care, with the knowledge that choosing our pharmaceutical products means unparalleled quality and reliability.