We Facilitate to

• Design your product as per current regulatory requirements

• Act upon the gaps with appropriate control strategy.

• Captivate market by successful DMF/ANDA filings.​

Specialized pharma analytical consultancy to Pharmaceutical industry and/or its subsidiary alliance across various functions                                                                                                                                              

Provide independent expert opinion /testimony related to polymorph charecterisation and interpretation in patent litigations for pharmaceutical or chemical industry.

Training could include topics like ICH guidelines, Analytical techniques, Impurities, Control strategy, Analytical Method validation, Data Integrity,  regulatory guidelines etc                                         

Audit and confirm compliance of Active substance and starting materials are in line with ICH Q7.                                                                                                                                                                               

Preparation of Drug Master File. Control strategy & GAP assessment for DMF Filing

We have Expertise in calculating PDE/OEL for cleaning validation           

Partnership for formulation development  Set up of manufacturing unit Alternate


We provide scientific expertise to three different labs that are our trusted “Testing partners”