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Consulting Services
ImQuest professional staff are always available to provide expert guidance and consulting services to assist with your drug development program. With our preclinical, clinical and regulatory consulting services, we can assist your company with the rapid and efficient development of your therapeutic agent from initial discovery and development through the IND and human clinical trials. |
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Grant and Contract Proposal Services
ImQuest BioSciences staff has a great deal of experience with the design and submission of NIH grants and contract proposals. In our service based operations we provide proposal writing services as a fee for service. |
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| IND and Regulatory Services |
| Strategic Scientific and Regulatory Planning for Therapeutic Development |
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Preclinical and Clinical Milestones and Timelines: We can develop a detailed plan to show what needs to be done and when it needs to be done. We can assist you with defining how the required work should be done and who should perform the studies. |
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Characterization of the Competitive Therapeutic Product Environment: We can evaluate competitive existing products that will have an impact on your development planning based on our years of experience in the therapeutic development arena and our intimate understanding of FDA requirements for approval. |
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Costing of Development Through Phase III Human Clinical Trials: Our strategic planning will provide you with detailed costing that can be used for your internal strategic planning and prioritization, as well as providing much needed information regarding investment needs. Your investors want answers and our strategic planning documents will provide you with what you need to know. |
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Preclinical Pharmacology, Toxicology, Chemical Manufacturing, Clinical Trials and Regulatory Liason: Our strategic planning documents will provide you with nuts to bolts details on the therapeutic development process and we will assist you every step along the path. We can provide vision or an unbiased third party review of your planning. |
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Customized Assay Development, Optimization and GLP-Validation: Make ImQuest your one stop to solve your therapeutic drug, vaccine, microbicide, protein, peptide, antibody, or biologic development needs, from discovery through clinical trials. |
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| ImQuest BioSciences has a proven track record of providing support to effectively move compounds from the discovery phase to preclinical IND-enabling studies for human clinical trials. Our expertise in infectious disease, cancer, immunology, and inflammatory disease is deeply founded in our core scientific capabilities in microbiology, cell biology, molecular biology, protein production, biochemistry, and enzymology. |
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| Copyright © 2006, ImQuest BioSciences. | | | |
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