We, The  PharmReg Neoteric formerly known as NR PHARMREG submission and consulting team, compile, publish and manages
IND (Investigational New Drug), 
NDA (New Drug Application), 
ANDA (Abbreviated New Drug Application), 
DMFs (Drug Master Files), 
ASMF (Active substance master file procedure), 
CEP and also BLAs (Biologic License Applications) dossiers for global regulatory authority such as FDA, EMA, MHRA, GCC, Health Canada, SAHPRA, JFDA, AUTGA, SWISSMEDIC.
Pharmacovigilance - PV department Setup, QPPV, Case processing, PADER writing support

PharmReg Neoteric

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