Clinical Trial Development in India
The modern changing lifestyle and its chronic ailments are the principal reasons why we need better medications and treatment processes. This is the reason why medical institutions and clinics must give importance to clinical trials and medical researchers to come with advanced drug development processes and innovative treatments. The Indian subcontinent over the past few years has recorded a quick and steady expansion in the domain of Clinical Trials. This itself proves that India is fast becoming one of the most desired destinations for medical research and advanced clinical studies. As the number of applications for research and study is rising, clinical trials and researches too are expected to increase in the forthcoming years. According to a report on “Booming Clinical Trials Market in India”, the expansion of clinical studies by domestic and international medical institutions has gone up in the recent times. Due to this progress, clinical trials in India are expected to touch the mark of 1950 by 2013. One of the important reasons for this expansion is the upsurge of the industry-sponsored trials that are an important aspect of clinical trials. Apart from this, few other factors such as stable medical architecture and skilled professionals will also improve the percentage of forthcoming medical trials in India. Recently, there have been various Clinical Research Organizations (CRO) in India that conducts clinical trials, especially focusing on the Phase I studies. Therefore, they have strategic liaisons with reputed hospitals, clinics and medical institutions. This ensures that the CRO also have the access to vast databases that spans across multiple therapeutic areas to other proprietary therapies and diagnostics. The majority of Indian CRO’s has their own research programs that execute the advanced and innovative new age study designs in Pharmacokinetic analysis, clinical pharmacology, and bio-analytical processes that are carried out by a team of expert and experienced clinical coordinators and research associates. Furthermore, they generally adopt a 360 degree approach towards clinical trials that make sure that the sponsors actually benefit from a host of services such as: * Pharmacy Services that assures a strict adherence to GCP and other allied international regulatory requirements * Feasibility Studies * Clinical Trial Supplies & Management * Bio Statistics * Project Management * Clinical Monitoring * Volunteer Recruitment & Planning Indian CRO’s in addition to Clinical Trials also focuses on Bio studies. This comprises multiple studies on bioavailability and bioequivalence are carried out in multiple centers staying in compliance with international regulatory needs managed efficiently by an independent quality assurance section.
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