At Auriga Research Analytical Division, Quality is defined in terms of various operational and functional parameters catered with standardized specification and customer's need. The objective of our dedicated Quality Assurance Team is to ascertain the application and implementation of these quality control standards. Our comprehensive SOPs provide the relevant framework to ensure standards are constantly maintained and continually improved.

At Auriga Research Analytical Division, anything less than perfect is unacceptable and the sole purpose of our Quality Assurance Team is to assure the level of excellence. Our operations are meticulously monitored by internal Quality Control Department to assure GLP compliance & stringent quality management. Our comprehensive SOPs provide the framework to assure standards are always maintained.

Auriga Research Limited (ARL) team understands the importance of managing the accuracy and quality of data in clinical trials. We ensure clinical data accuracy and integrity by thorough review of the data, to assess the validity of outlying data points, and to carefully document query identification and resolution throughout a study's duration. Quality assurance Unit (QAU) performs periodic operational checks to ensure trial related activities were appropriately conducted and that the data were generated, recorded, analyzed, and accurately reported according to protocol, standard operating procedures (SOPs), and good clinical practices (GCPs).

Auriga provides optimum emphasis over Quality Issues, some of them are as follows:

• Orientation and periodical training of personnel for skill development and professional improvement.
• SOP-based systems with periodic reviews to adopt to changing regulatory and industry requirements.