Testing service support
Raw material,Impurity profile,Metals analysis,Pesticides and residual pesticides.
Finish goods (FMCG products, Pharmaceutical products, Food products, metals).
Clinical research (BA BE study, phase 1, phase 2, phase 3, phase 4, phase 5 trials).
Impurities in Raw materials and its method.
Identification of unknown compounds/ material.
Supports for all types of testing from NABL, GLP, Agmark, FSSAI, BIS, FDA, and USFDA accredited laboratories in reasonable negotiated rates with high quality results in minimum time.
Stability studies of pharmaceuticals and non-pharmaceuticals products and raw materials.
Safety evaluation of products and Intermediates etc at ppb level.
Identification/ quantification of unknown impurities like Aflatoxins, PCBs, Dioxan, volatile organic impurities, chrom III, Chrom VI and other impurities.
New method development and Validation. Process validation Cleaning validation
Formulation support
To provide cheaper formulation support with best performance.
Resolution of formulation issues.
Setting up specifications .
Setting up method of manufacturing.
Setting up of bill of material.
Audit preparation support
Training on audit process for laboratories/ manufacturing units.
Preparation of documentation by deputing trained man power.
Standard operating procedure.
Quality management system.
GLP documentation.
FDA documentation.
USFDA documentation.
NABL docuementation.
Health and Safety at work place.
Regulatory support
To provide end to end support to resolve regulatory issues.
Claim Support
To provide the scientific proofs for claim support on the product label.
Registration support
To guide for the generation of data/ records for registration.