Wherever you are, COD Research can help you across all the phases of your clinical research with a scientific perspective and distinct approach in order to achieve perfection. Here is a scope of the phases in which we hold a professional finesse.
Early phase trials describe the first test of the drug candidate’s clinical performance and may look at whether a drug is safe and tolerable along with its clinical pharmacology and biopharmaceutical properties. Early phase trials conclude the drug candidate’s efficacy, safety, and positive impact on the patients.
Subsequent phases of clinical trials aim to investigate the drug candidate’s exploratory and confirmatory clinical performance, which may include either discovery of a new treatment or the creation of an option for existing treatments.
○ Protocol Development
○ Scientific Advice and Consultation
○ Statistical Design
○ Data Management
○ Clinical Monitoring
○ Data Analysis and Clinical Study Reports
● A dedicated team of early phase trial professionals help to execute, accelerate your trial and contain costs.
● Unique access to global patients via Accelerated Enrollment Solutions.
● Our channel partners support early phase trials, including bioanalytical and pharmacokinetic analysis.
Steering the convolutions of Phases II and III of your clinical trial can be challenging. We’ve integrated the disciplines that we know how to focus on end-to-end clinical development on time and within budget, and we clearly understand that these two are vital for the success of the clinical trial.
Our highly personalized services and our research professionals’ expertise are capable of meeting multiple milestones, solving recruitment challenges, monitoring safety and effectiveness, and so much more.
We offer enormous global impression and clinical development solutions that span several therapeutic and service areas in accumulation to various outsourcing models to meet the definite needs of our patrons.
We understand that phase IV is an important phase of drug development, to know the real-world effectiveness of a drug as evaluated in an observational, non-interventional trial in a naturalistic setting which complements the efficacy data that emanates from pre-marketing Randomized Clinical Trials (RCT).
Our association with potential investigator sites and the experienced study team will help in undertaking different Phase IV studies, including PMS, Registry, Non-Interventional, Drug Utilization studies as well as, Adverse Event Monitoring, and many more.
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All clinical trials come with their own set of unique complexities. You need an innovative CRO partner that can help guide you through these challenges and see your trial to its completion timely and effectively. Discover how COD Research's contract research expertise can help.