Join the Program on Risk Based Monitoring (RBM)
Category: Clinical Research
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Opportunities for a Data Clinical Manager
Clinical Data Management or CDM is an important area of clinical research and studies. Healthcare organizations and hospitals employ Clinical Data Managers for their organizations.
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Environmental Monitoring using Risk Based Approach
In order to routinely monitor particulates and micro-organisms in critical areas of a pharmaceutical manufacturing plant, more particularly in the aseptic processing areas, the environmental monitoring (EM) program has been designed, which comprises of viable and non-viable monitoring elements.
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Mobile Data Capture in Clinical Trials: An Overview
The introduction of mobile device-based electronic data capture system (mEDC) technology is indeed a boon for clinical trials, as per a research report. According to the new research paper published by the Journal of Medical Internet Research, the mobile device is of immense help in terms of supporting a slew of services within clinical trials such as project management, tele-monitoring, and data management, among others.
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6 Healthcare Revenue Cycle Management Systems to Watch
Healthcare organizations and hospitals are engaged in providing the healthcare services all the time. These services are crucial for treating, monitoring and assisting patient well-being. They take care of patient requirements from admitting, treating, scheduling appointments and providing specialized services.
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Risk Based Monitoring Workshop by Dr. Nimita Limaye
Join us for an in-depth session on Risk Based Monitoring Workshop by Dr. Nimita Limaye!
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Risk Based Decision Making – An overview
Drug safety industry is on the verge of comprehensive analysis phase to determine the possible conditions and process involved in risk-based decision making. Pharma industries take a leap to advanced mechanisms that are systematically approved for implementation. It can be assessed based on its post-marketing strategies which are completely based on regulatory decisions. Improved information statistics to the risk-based decisions appear to be ad hoc, informal and qualitative. The more systematic and scientific behavior is risk-based assessment that could be used for the employment of thorough drug safety efficacies. Possible recommendations of assessments in the drug safety industry include the corresponding behaviour analysis of drugs directed towards the FDA in the preapproval and postapproval settings.
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What is Openclinica?
Openclinica has been known as the world’s first commercial open source clinical trial software serving for the purpose of clinical data management (CDM) and electronic data capture (EDC). Openclinicia is immersed in clinical trials and different types of clinical research areas.
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End to End Patient Engagement in Clinical Research
Complete involvement of patients in their personal healthcare is known as End-to-End Patient Engagement. In today’s world, this is primarily accomplished electronically through Patient Engagement Technology that involves hardware, software, and services. This technology is an important tool for clinical research and trials.
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Migrating CRF to eCRF
The necessity to upgrade case report forms (CRFs) happens often during the course of a clinical trial. As a result of advancement in the world of electronic data capture methods, the requirement for Electronic case report forms (eCRFs) has been increased significantly. One should analyze the root cause to such updates in electronic case report forms to acquire efficient knowledge about the migration of case report forms to electronic case report forms. Factors such as protocol amendments, optimized changes made to the eCRF specification requirements and the logic responsible for the automation of the entry or verification of data during the course of study substantiate the needs to migrate to eCRF.
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Case-Control Study in Research
A case-control study is one of the methods of determining the risk factors involved in various kinds of diseases, their exposure, and vulnerabilities. It is an important method of conducting clinical research or clinical trials.
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Five Digital Innovations to Enhance Clinical Trials
A Digital innovation is the application of new technologies to offer solutions for existing business problems, issues. and practices. It is the application of digital tools offering an enhanced customer experience and solutions to any challenges.These are breakthrough innovations that help in creating world-class solutions. Digital innovations speak of the great change in every sphere of life. Digital innovations and digital develop are crucial to the success of any enterprise in the future.
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Advantages of Electronic Health Records (EHR)
A major shift in the adoption of technology has been observed in the healthcare sector in the recent years. Many healthcare facilities including hospitals and private clinics have started using Electronic health records for the betterment of medical care to the patients. Since it can be largely accessed on demand and also a major benefit to practitioners, the technology has flourished to a larger extent saving lives. Experts affirm that Electronic health records could be seen as the technology with significantly less number of errors when compared to paper records.
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Electrocardiographic Data in Clinical Trials!
In today’s world, the amount of data collected while conducting clinical trials is massive. This data needs to be converted into meaningful and usable information by experts to develop an accurate benefit -risk profile for any drug under research or study. The success of any clinical study or trial is highly dependable on the correct interpretation of collected data.
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Patient Recruitment – A Synopsis
Development of a new drug is an expensive and time-consuming procedure. Any drug can be brought to market only after completion of successful clinical study about its benefits and side-effects. These studies are elaborate, detailed and many time long-term.