Everything in the world today goes paperless; to your surprise the paper work carried to conduct the clinical trials in world of technology produced 100,000 pages of documents. It is very important to take the effective measures to reduce the paper work and increase the efficiency of the clinical trials. Integrating clinical trials with the technology will reduce the time to the market.
Moving to paperless clinical trials involve some challenges too. For the paperless clinical trials to be successful they have to be secure, stable, scalable and should be supported both internally and externally. To bring the paperless clinical trials into reality, content management system should have industry-wide agreement on the technologies, standards and protocols and business processes. Contributing to the paperless clinical trials, solutions should integrate with other application and seamlessly integrate the data from different sources into common, accessible formats in order to improve the data exchange and foster the collaboration. Paper less clinical trials stand as norm when they abide the regulations of FDA apart from increasing the efficiency of the clinical trials.
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