Method Development & Validation
EuTech Scientific Services, Inc. has over two decades of experience in method development and validation. Our expert technical staff enables us to develop and validate specialized methods of analysis for a number of products such as yours. We adhere to GLP guidelines provided by the FDA. Our state of the art laboratory is equipped to meet all your analytical needs. EuTech Scientific Services, Inc. offers reliable and accurate method validation services.
EuTech Scientific Services can be entrusted with all your method development and validation projects. Our protocols are flexible and can be designed to meet your specific needs. EuTech staff prides itself on providing accurate, dependable data in a timely, cost and effective manner.
Analytical Characteristics Used to Define Our Method Validation:
- Detection Limit
- Quantitation Limit
Contact us for the following services:
- Chromatographic Techniques including: HPLC, GC, GC-MS/MS, LC-MS/MS, ICP-MS and FTIr Spectroscopy
- Protocol Validation and transfer
- Residual Solvents
- Extractables/ Leachables Studies
- Trace Organics
- Forced degradation studies
- Stability Studies
- Details of active ingredients
- Impurity profiling and identification