RRC has an independent Quality Assurance (QA) department which mainly works on standard operating procedures writing and Registration Documents.

Standard Operating Procedures (SOP’s) writing

Standard operating procedures for laboratories and manufacturing units can be developed in order to meet the regulatory requirement and to establish the GMP/GLP at different levels

Registration Documents (DMF’s, Dossiers)

Dossiers are developed based on customer requirement and registering countries. The analytical, stability and validation work associated with dossiers are performed In-house

Drug Master File’s based on European Common Technical Document (e-CTD) format are developed at RRC

Structural Elucidation is the essential part of DMF. Our team has well experienced scientists having good knowledge of structural elucidation