Components of Medical Phase I Studies
Clinical researches and trials include numerous medical tests, experiments and medical studies. An eminent branch of studies is Phase I Studies and researches that involve new diagnosis, treatment and analysis of the drug used on patients. The primary objective of these studies is to learn and study about the apt dosing schedule. Furthermore, the study comprises objectives that analyses the way in which a particular drug has been given, the amount of drug as well as the frequency at which it is allotted to the patient. Medical researchers and technicians focus on updating themselves about any drug and its toxic and other harmful impacts.
Notable Indian clinical research organizations carry on Phase I Studies that are assisted by their vast experience in Clinical trials. These research organizations arefurnished with the latest state-of-the-art medical infrastructure and also have medical volunteers who help in these studies. Some of the components comprise of the following:-
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First-in-human
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Single Ascending Dose studies
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Multiple Ascending Dose studies
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New Chemical Entities
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Dose Escalating studies
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Capabilities
Apart from the services mentioned above, renowned clinical research organization’s in India also comprise Phase I Studies in First –in-Man for the New Chemical Entities (NCE’s) and also the New Biological Entities (NBEs). Furthermore, there is a vast array of medical pharmacology studies that includes Drug inspection studies, Food Effect, Proof of Mechanism & Proof of Concept, TQTc studies, Pharmacokinetic/Pharmacodynamic studies and other allied explanatory studies for various biomarkers and Special Popular studies.
Apart from diverse medical services and researches, infrastructure too plays a crucial role in Phase I Studies. Most clinical research organizations are well equipped with bed units that are efficiently managed by a group of trained professionals. These professionals have the needed medical expertise and are furnished with state-of-the-art clinical devices. In addition to this, there are trained experienced physicians and nursing staffs. They have hands on experience in conducting First-in-human and other clinical Pharmacology studies.
Clinical Research Organization’s (CRO) have the experience in conducting medical trials and researches in special and patient populations. The service range spans across Phase I to III studies for numerous biotechnology and pharmaceutical studies and assists in end-to-end Clinical Trials. Apart from this, there are other services that they offer, such as Bio Studies, Medical Writing, Biometrics, Regulatory Compliance Services and Bioanalytical Research and have an excellent track record for their services, client feedback and testimonials.
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