Our R &D team consisting of Pharmacologists, microbiologists, botanists, and natural-products chemists work constantly to identify phyto-bioactive leads that could be developed for treatment of various animal diseases.
There is a standard formulations development process. R & D division selects botanicals/medicinal plants based on scientific literary review & ethno-botanical studies, then a study of Morphological & physio-chemical properties of the medicinal plants is carried out, it is followed by the preparation of different solvent guided extracts. The extracts are later characterized phytochemically & a detailed Bioassay /in vitro efficacy is carried out to study the specific functions response. Best extracts are later identified. The next step which follows is fractionation & sub-fractionation of most effective extract & identification of effective fractions/sub-fractions which is followed by standardization of extract & identification of marker compounds. After this, safety & stability studies are carried out; which are followed by in vivo studies/efficacy of the extract on natural host against experimental challenge infection/affection & data analysis. Finally, formula is prepared & validation of results is done through 3rd party testing of efficacy under field conditions .
To ensure highest safety & efficacy, Proper double-blind clinical trials are conducted to determine the safety and efficacy of each formula before they are recommended for medical use. Toxicity studies are conducted as per Guidelines of OECD.
In order to smoothly carry out the innovation & development, & quality assurance activities our labs are equipped with modern cutting edge technologies.