The quality of clinical trial data and clinical trials has been deteriorating continuously over the years. To preserve this proficiently, several CDM organizations have evolved to improve data leadership working within a digital environment with more tactical and prolonged functions. During the process of coding and reconciliation, patient data collection…
Pharmaceutical industry experts today are stimulating pharmacovigilance service providers to supply a greater value for the funding they provide. Not surprisingly, service providers are addressing this need by investing in technology and automation tools that are poised to increase both the efficiency and quality of pharmacovigilance operations. Artificial Intelligence (AI),…
Who is a CRC? A Clinical Research Coordinator (CRC) is a person responsible for conducting clinical trials using good clinical practice (GCP) under the instructions from a Principal Investigator (PI). A health care professional who, under the supervision of the investigator, submits all research documents to IRB, schedules and implements the study visit requirement, co-ordinates all…
