Clinical

MakroCare manages clinical development through its qualified professionals and experienced staff at global level. Our qualified and experienced teams manage full service studies for pharma, biotech, medical devices and nutrition from study design and feasibility to patient recruitment, clinical monitoring, data management, statistical analysis, safety reporting, to worldwide submission of applications in accordance with the regulations set forth by the USA, Canada, UK/EU, Singapore, China, India, Japan, Asean, ICH and other regulatory agencies.