ChemDiv chemistry of cures

ChemDiv offers full clinical services to oversee and conduct your clinical trial in Russia, Ukraine and Baltic States. Our expertise ranges from Phase I to Phase IV and within multiple therapeutic areas. Our highly qualified clinical Project Managers will work with local Key Opinion Leaders (who are often used as principal investigators) to design a clinical trial that meets the clients needs and that can ensure fast enrollment and high quality data. All work is completed under ICH Guidelines and follows GCP so that all data can be submissible to the EMEA and FDA. We work with the client and our internal and external vendors in a fully transparent model of joint partnership in order to make your clinical trial a success. We can provide medical writing, regulatory, monitoring, project management, vendor management, drug storage/shipment/destruction, data management and biostatistics whether it is utilizing our internal resources or trusted partners.  We can also integrate with other CROs to increase recruitment of patients in Russia, Ukraine and Baltic States.

Find attached:

ChemDiv-Clinical_Development.pdf

See Also:

Clinical Trial Management
Clinical Trial Monitoring
Quality Assurance Control
Late Stage Research Services