Frequently Asked Questions
General Questions
Kshetra Analyticals provides bioanalytical services, analytical services, analysis of pharmacokinetic and toxicological studies, forced degradation and stability studies, and method development and method validation.
The bioavailability and bioequivalence center at Kshetra Analyticals supports clinical research during the product development stage by conducting Method Development, Method validation, and Bioavailability and Bioequivalence studies (BA&BE Studies).
Method validation is essential in bioequivalence studies to ensure that the analytical methods used are reliable, accurate, and precise.
Forced degradation is the process of intentionally subjecting a drug substance or drug product to harsh conditions to accelerate the degradation process and identify potential degradation products.
The purpose of stability testing is to evaluate the stability of a drug substance or drug product under various conditions and to determine its shelf life.
Quality, Delivery FAQ
Kshetra Analyticals ensures the quality of its services by adhering to strict quality control procedures, regularly calibrating and maintaining its equipment, and having a team of experienced professionals who follow established protocols and guidelines.
The turnaround time for Kshetra Analyticals’ services varies depending on the specific service requested and the scope of the project. The company strives to provide timely and efficient services while maintaining high quality standards.
Yes, Kshetra Analyticals provides customized services tailored to meet the specific needs of its clients.
Kshetra Analyticals takes client confidentiality seriously and maintains strict confidentiality policies to protect the privacy and proprietary information of its clients.
Kshetra Analyticals values its clients and provides prompt and efficient customer support to address any questions or concerns that may arise.