Clinical Consulting Services

Cedent's Clinical Consulting division is a leading Trial Management Organization. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. We have an extensive collaborative global reach and can offer all clinical research services globally.

For complex global trials or focused regional studies in all phases, talented clinical trial management team makes all the difference in how well the trials are initiated, conducted and closed. Trial management is one of the core services at Cedent, we are focused on providing on-time, on-budget, quality deliverables with high transparency to achieve our client’s goal.

Our dedicated CRAs provide consistent and effective monitoring and interaction with study sites. We can provide qualified, trained and experienced regionally based Clinical Research Associates (CRAs) who has an average of 1 to 10+ years monitoring experience in any therapeutic area. Our clients utilize one CRA to any number at a given point of time.

Cedent consultants bring the expertise and experience you need to continue deliver innovative therapeutics to the market successfully. With an experience of consulting across wide range of therapeutic area, our science, medical, clinical, data, safety, biostatisticians, medical writing and regulatory consultants have broad understanding of market landscape and regulatory requirements. We also have deep experience in the area of rare diseases and pediatric indications, as well as in the development of medical devices, drug device combinations and companion diagnostics.

Complexities of running the clinical Trials and meeting the projected timelines with in the budget – these impact the business cycle and more importantly, the capacity of the organization to get ahead of the competition. The fundamental blocks of building and running a Global Clinical Trial will not be complete without a competent and dependable workforce. We are a unique service provider for Pharma/Biotech/Device companies, CROs and Clinical sites who are seeking to build its drug development Team whether on contract, contract to hire or permanent hires.

At Cedent, we believe that people are the best asset, regardless of the business size, industry and market share. We provide the best Clinical Research Professionals, backed with solid years of expertise, experience and knowledge, who can integrate solutions for your business needs. We understand that you are working aggressively to bring your pipelines to the market. We will be the right partner to work along and manage your Clinical studies.