Butterworth specialise in Quality Control Analysis, Method Development, Validation & Stability Testing of Raw Materials, API, Finished Product and Medical Devices to cGMP. MHRA and FDA Inspected. Take a look at our brochure to find out more...
- Elemental Impurity Analysis in Pharmaceuticals – The Road To Implementation of ICH Q3D
- Enhanced Sampling and Calibration Procedures for the Analysis of Residual Oxygen in Nitrogen Purged Pharmaceutical Packaging by GC-TCD
- Enhanced Residual Solvents Analysis: A Practical Approach to Sampling, Delivery, Storage and Analysis.
- A Method to Meet the New Ph Eur Ninhydrin-Positive Substances Requirement