In initial stages of drug Development very less is know about the new formulation. Hence such initial studies are carried out in animal for testing its safety and efficacy. Once the results of animal studies are satisfactory further research can be carried out in humans.

If you have different combinations to be tested, animal studies gives you a chance to study them simultaneously and to select the most suitable one for further development in clinical trails.

We have full-fledged animal house accredited by the Committee for Prevention of Crurelty  in scientific Experiments on Animals (CPCSEA), India. We follow all procedures of CPCSEA guidelines for animal handling and maintenance.

We have a team of experts to carry out various toxicity and efficacy studies.

We also have CPCSEA registered Ethics Committee.

We have a full- fledged central research lab, which plays an active part in research and development as well as quality control.Central research lab has three different sections

1. Chemistry
2. Microbiology
3. Pharmacognosy

All the procedures are carried out by experts in respective fields.
Central research lab is having facilities for following

1. Identification and isolation of phyto chemicals
2. Extraction of phyto chemicals
3. Microbial testing
4. Identification of crude drugs using pharmacognostic techniques.
5.  Authentication and certification of raw drugs.
6. Quality assurance.
7. Testing of impurities: Foreign matter, adulterants, heavy Metals, Pesticides, Physico-Chemical analysis, Residual Solvents, Alfa toxins, Microbial limits, ect
8. Formulation Standardizationz

Clinical trial agreement needs careful review and consideration for making the partnership in research more reliable we maintain a policy to undergo a memorandum of understanding (MOU) with the sponsor after careful  revive and consideration, which will ensure transparency in the job and will assure that the work gets completed in a pre planned manner and in stipulated duration.

Per—clinical studies give lot information regarding safety and efficacy of the drug. There are chances that the drug may behave differently in humans than as compared to animals due to various reasons lie different metabolic pathway. Hence Clinical trails are very important part of total drug development program. It actually tells you where your drug stands when it comes to treat the patients. Hence it is absolutely necessary that the study is conducted strictly in a scientific manner and according to GCP guidelines. Hence your study needs periodic monitoring.

We know that your job of clinically testing the drug is a challenging, and you cancompletely rely on us to deliver timely and error free results, within the desired budget.

Our clinical and project management teams provide integrated planning and implementation from start to end of the study.

Our GCP trained monitors will involve periodic monitoring of the ongoing study along with corrective action if required, and will ensure that the study is conducted as per protocol and GCP guidelines, which will assure you the most reliable data.