Clinical Trial Services

Early Phase Clinical Development Early Phase Clinical trials are an important and necessary aspect of the drug research/clinical development programme for understanding the nature, PK/PD, safety, and POC of a novel medicine. Further clinical studies might be planned based on the data gained on safety and efficacy. A phase I clinical study allows for an early assessment of the product’s safety and tolerability characteristics. Phase II to Phase IV Clinical Trials To ensure patient safety, our clinical trials team assists our clients with study feasibility, pre-site qualification, Site initiation, interim monitoring, and study closure visits, patient recruitment services, site management services, and study monitoring (including Central Monitoring, Remote Monitoring, and On-site Monitoring). Our well-trained and skilled Project Managers, Senior Clinical Research Associates, Clinical Research Associates, and Clinical Trial Assistants have worked with over 350 clinical investigators and have years of clinical monitoring expertise in a variety of therapeutic areas. Our project managers have a successful track record of completing trials on time and within budget. ICBio has completed various Phase II and phase III clinical trials. ICBio has experience of handling studies in various therapeutic segments- Oncology, Psychiatry, Dermatology, Rheumatology, Gastroenterology, Cardiology, Ophthalmology, ENT, Gynaecology, etc.