Our highly qualified quality control staff are well experienced to handle GXP, develop methods in accordance with the principles of Analytical Quality by design includes analytical transfer, Analytical method development, dissolution profiling, Impurity profiling and define strategy as per CCS to meet the regulatory standards.
The Quality Control Laboratory is capable of sampling, testing of all starting materials, packaging materials, In-process and Finished products Samples in accordance with current pharmacopeial specifications or established standards. Quality control ensures documentation and release procedure as per marketing authorizations. Outside reliable approved contract testing laboratory support are taken for specific tests and results are reviewed by authorized staff prior to release of the Material/ products as per Marketing authorizations.
The Quality Control laboratory is fully equipped with the most sophisticated and modern analytical instruments for chemical and instrumental analysis and equipped with Microbiological Testing.
Our Quality Function is independent from manufacturing and authorized to take appropriate decisions on all quality matters. Quality Control is an integral part of cGMP and ensures that necessary and relevant tests are carried out. No material and products are released for use until the quality has been judged satisfactory for their intended purpose.