Novel Drug Discovery
      (Molecular Modeling & Computer Aided Drug Design)

We are carrying out the projects on Cancer, HIV/AIDS, Diabetes, Hepatitis, Influenza, Schizophrenia, Malaria, Parkinson's disease, Alzheimer's disease, Cardiovascular, Measles, Tuberculosis by initiating from the Gene sequence of the patient and finally evolving with a suitable drug for curing that disease. Project comprises of Computational Genome Sequence Analysis, Phylogenetic Analysis, Protein Sequence Analysis, Homology Modeling, Protein structure prediction, Molecular Modeling, Computer Aided Drug designing, Virtual screening and Docking.                              >>readmore             

Eligibility:

• MBBS, MD,BDS, BHMS, BUMS, BAMS, BPT
• M.Sc.,(Microbiology/Biochemistry/Biotechnology/Bioinformatics/Chemistry/Genetics/ Botany/Zoology/Life Sciences)
• B.Pharmacy, M.Pharmacy, B.Sc., B.Tech.(Biotechnology)

Clinical Research

A new blockbuster drug takes around $850 million to be developed by an international giant. Nearly 70% of which goes towards clinical trials. In the area of clinical trials, India, with its vast and diverse, disease patient population, is now showing competence at nearly a third for the costs compare to the west.

The most commonly performed clinical trials evaluate new drugs, medical devices, biologics, or other interventions to patients in strictly scientifically controlled settings, and are required for regulatory authority (in the USA, the Food and Drug Administration) approval of new therapies. Trials may be designed to assess the safety and efficacy of an experimental therapy, to assess whether the new intervention is better than standard therapy, or to compare the efficacy of two standard or marketed interventions. The trial objectives and design are usually documented in a Clinical trial protocol.                                                  >>readmore      

CDM - Clinical Data Management

CDM (Clinical Data Management) is used in clinical research to manage the data of a clinical trial. The clinical trial data gathered at the investigator site in the case report forms are stored in CDMS. CDM (Clinical Data Management) comprises of designing and deploying clinical study as well as collecting data and managing data for that clinical study. Electronic Processes are used to plan, collect, access, exchange, manage and archive data for the purpose of reporting the entire clinical study data. Adoption of CDM to drive forward drug research is gaining pace, championed by the pharmaceutical industry, primary health providers, CRO industry & USFDA regulators.