At Minerva Scientific our experienced team of dedicated scientists are able to offer the broad range of test requirements demanded by todays Pharmaceutical and Healthcare industries. Our focus on rapid delivery of high-quality results ensures clients meet critical deadlines.
Our modern laboratory facilities are fully MHRA approved for GMP operation – refer to our MHRA letter of authorisation for further information.
The main areas in which we operate can be found in the following list; however, this list is not exhaustive so please contact us if you have specific requirements that are not covered below.
- Product Release Testing
- Metered-Dose Inhaler (MDI) Testing
- Cytotoxic Product Testing
- Residual Solvent Testing
- Pharmacopoeial Testing (BP, EP, USP)
- Method Development and Validation
- Stability Testing and Storage to ICH Guidelines
- Problem Solving and Investigative Analysis
Please refer to our statement on provision of services to customers for a general outline of our service level and customer responsibilities.
Details on sample submission can be found in our important shipping information.