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The duties of the clinical trial date management is to keep track of everything that takes place during a clinic trial. This ranges from how the patient feels and all their symptoms to documenting concerns.

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What industries use a clinical trial management system?

The clinical trial management system is used in biochemical, pharmecutical industries and clinical research institutions. The system itself is used to correlate large amounts of data concerning the clinical trial.


What is clinical trail management software?

Clinical trial management software is a specialized tool used to plan, track, and manage clinical trials efficiently. It helps in organizing study protocols, patient data, regulatory compliance, and reporting. A robust clinical data management software ensures accurate data collection, monitoring, and analysis, improving the overall efficiency and reliability of clinical research.


What is clinical trial data services?

Clinical Trial Data Services (CTDS) are an organization that focus on clinical research. The organization also provide understanding about clinical trial processes, for example.


What is data cleaning in clinical data management?

Data cleaning in clinical data management (CDM) refers to the process of identifying, correcting, or removing inaccurate, inconsistent, incomplete, or irrelevant data from clinical trial datasets to ensure data quality, accuracy, and reliability.


What has the author Susanne Prokscha written?

Susanne Prokscha has written: 'Practical guide to clinical data management' -- subject(s): Clinical Pharmacology, Clinical trials, Data Collection, Data base management systems, Data processing, Database management, Drugs, Information management, Methods, Organization & administration, Testing


What is the work of a clinical trial assistant?

A clinical trial assistant (CTA) supports the planning, execution, and monitoring of clinical trials. Their responsibilities include managing trial documentation, coordinating communication among team members, ensuring compliance with regulatory requirements, and assisting with data management. CTAs also help maintain study supplies and may prepare reports to track trial progress. Overall, they play a crucial role in facilitating the smooth operation of clinical research projects.


What companies offer clinical data management?

There are many companies all over the world that offer clinical data management. These vary from the very large corporations such as IBM, to SGS and QAS.


What is clinical research software used for?

Clinical research software is used to manage large amounts of data involved in the daily operations of a clinical trial. It often provides data to business intelligence services.


What is the main function of ClinPhone?

ClinPhone is a technology platform primarily used in clinical trials for managing and streamlining the process of randomization and trial supply management. It facilitates patient enrollment by providing tools for electronic data capture, randomization algorithms, and real-time monitoring of trial progress. By improving efficiency and accuracy in trial management, ClinPhone helps researchers and sponsors ensure that clinical studies are conducted effectively and in compliance with regulatory standards.


What software can be used to store clinical data?

A clinical data management software system (CDMS) is used to store clinical data. It is specially designed software built to reduce the possibility of incorrect data entry due to human error.


Difference between Clintrial and oracle clinical software?

That is a complex question. Both are clinical data management systems used by hundreds of companies. Both products are now owned by Oracle. Clintrial is more modular and has separate tables for each trial where Oracle Clinical is more robust and has consolidated data. Both have numerous interfaces and add-on functionality. They are both Oracle Based and web enabled.


What are three things a clinical trial would include?

A clinical trial typically includes: a detailed protocol outlining the study design, methods, and objectives; informed consent process to ensure participants understand risks and benefits; and data collection and analysis to determine the safety and efficacy of the intervention being studied.