Regulatory Affairs

? Should be well versed with Regulatory Guidelines of South East Asia, Africa, Middle East, LATAM, CIS Countries (ROW Market) ? Knowledge of Preparation ,compilation & review of CTD , ACTD & ECTD Dossiers. ? Should be well versed in Handling customers & MOH query with respect to technical documentation (Stability Data, GMP, FSC, DMF etc.) ? Well versed in IP /BP /USP pharmacopeia. ? Should have a knowledge of applications of product permission , FSC, COPP ? Should have knowledge of Loan License…