We manage simple and complex clinical trials.
Site feasibility assessment
Handling all site related activities and monitoring work
Complete responsibility of clinical Data management process for multiple clinical trials.
Data analysis and reporting.
Database quality checks and data validation.
Data Analysis, Data Mining & Secondary Research.
Acquisition of data from internet, Case Report Forms (CRFs) & Data Clarification Forms (DCFs)
Collect & analyze the information about marketed & development stage products of Pharmaceutical companies including clinical trial data, regulatory information (approvals & filings of NDA, BLA etc), press release tracking & analysis, Deal-M&A (mergers & acquisitions), patent updates capture for products & companies from various secondary sources like company websites, regulatory sites, Clinicaltrials.gov, SEC filings, annual reports, scientific journals, healthcare conferences and annual meetings like ASCO, ASH, SABCS etc.
Wide variety of public & proprietary data bases: FDA, EMEA, ClinicalTrials.gov, NCI, CTRI, UMIN, Medscape, PubMed, Science Direct etc for trial related information of patients like patient segment, therapeutic area, target accrual, actual accrual, status of a trial, study design, inclusion and exclusion criteria, information of investigators involved etc.
Construct records for clinical trials conducted all over the world and extract out information from various therapeutic areas' annual meetings, journals, company registries, company press releases and countries registries.
Data entry of Phase II-IV clinical trials.
Perform web search of various clinical trials on various criteria that we follow in our work-process and assemble the data thoroughly and with high precision.
Manage your content writing, literature, social media.