Clinical Trial Services
Over the last 15 Years we made an impact that is strong in pharma industry.
Cito’s Clinical Development Services comprises of various services such as Bioavailability/Bioequivalence studies, Clinical Trials and allied supporting services for the pharmaceutical industry for their submission to regulated and semi regulated market. Having a basket of associates, Cito is uniquely structured to support the needs of healthcare industry during all stages of clinical development, whether be a complete bioequivalence study or a clinical trial management program. We are capable to provide you assured quality to answer your clinical need.
We organize for our associates various pre-clinical and Clinical Development Services.
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Pre-clinical
Expected studies on toxicity and others on small animals, large animals both in GLP and non-GLP environments.
Early Stages
Phase-I for those products manufactured in India Phase-I from Second cohort on-wards for those products manufactured outside of India. BA/BE studies on both healthy and patient populations
