Clinical Trials and Regulatory Affairs
Clinical trials generate data on safety and efficacy.
Such consequent biomedical or behavioural research studies on human
participants are designed to answer specific questions about biomedical or behavioural interferences, including new
treatments such as novel vaccines, drugs, dietary supplements, and medical devices. These
trials produce data on safety and efficacy. The regulatory affairs outsourcing market has been segmented
into five major service sections .Those sections include regulatory affairs, clinical
trial applications and product registrations, regulatory writing and
publishing, regulatory consulting and legal representation and others. The
market sections have been broadly scheduled on the source of their usefulness,
efficacy, and generated revenue and geographic revenue.
The market size and estimate in USD million for every service type for the period from 2010 -2020, considering 2013 as basic year. This report also delivers the compounded annual growth rate (CAGR %) for each market segment for the forecast period from 2014- 2020.