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The Statistician’s view of a Clinical Trial

The Statistician’s view of a Clinical Trial The typical flow of clinical trial data begins with the patient and ends with a clinical study report or publication. In between, data passes through a number of steps from collection to verification to analysis. Most stakeholders in

What is Real World Evidence

What is Real World Evidence? The relatively new practice of Real World Evidence (RWE) has proven to greatly enhance the quality and effectiveness of clinical studies. According to the FDA, Real world evidence is the clinical evidence regarding the usage and potential benefits or risks

What are Post Marketing Observational Studies

What are Post Marketing Observational Studies (PMOS) If you are planning a post-marketing observation study an effective CRO can align your data collection and analyses with your objectives and leverage their statistical expertise to mitigate the risks. What are Post Marketing Observational Studies? Before a

CDISC Data Standards SDTM and AdaM

CDISC Data Standards SDTM and AdaM Clinical Data Interchange Standards Consortium (CDISC), founded in 1997, is a global non-profit data standards organization that works for enhancing the impact of clinical research by developing data standards for the accumulation, analysis, and transmission of clinical data. CDISC

Clinical Trial Conferences to attend in 2022

CLINICAL TRIAL CONFERENCES TO ATTEND IN 2022 Please visit the updated page of Clinical Trial Conferences to attend by year As North America comes to terms with how to live with the Covid Pandemic, conference organizers are ramping up the 2022 year with

Download Whitepaper Take The Pain Out Of Clinical Trials

Whitepaper Take The Pain Out Of Clinical Trials As a research pharma or biotech, you face a complex and regulatory-heavy environment. New developing products make competition ﬁerce, while a trend in regulatory control of protocols and funding has created myriad challenges for building a case