OXUS TECHNOLOGIES Making Superior Technology Available and Affordable for All.
OXUS TECHNOLOGIES Making Superior Technology Available and Affordable for All.
OXUS CLINICAL RESEARCH ORGANISATION
BESPOKE DEVELOPMENT (Software, Database, Website)
OXUS CLINICAL RESEARCH ORGANISATION
BESPOKE DEVELOPMENT (Software, Database, Website)
INNOVATE TO SUCCEED.
OXUS CLINICAL RESEARCH ORGANISATION
OXUS CLINICAL RESEARCH ORGANISATION
DATA MANAGEMENT
We offer an end-to-end Clinical Data Management solution including rapid database (CRFs) design, system validation, real-time data cleaning, query management and resolution, effective external vendor data management, integrated clinical data sources, database lock, and clean.
DATA PROTECTION AND GOVERANCE
Our team has worked with national and international institutions supporting them compliance with GDPR and other complex legislative landscapes including DPIA, DSPT and DTAC.
REGULATION AND AUDIT (MHRA, FDA, EMA)
Oxus’s team of experienced QA, regulatory and clinical research professionals, dedicated to providing high quality, practical, responsive and cost-effective services to support institutions and pharmaceutical companies with early and late stages of clinical trials.
SYSTEM VALIDATION
Our experienced team of Software Engineers and consultants can provide guidance and training on the principle of system validation (e.g. REDCap, OpenClinca), regulatory compliant system documentation, validation plans and risk-based approaches.
CLINICAL TRIALS APPS
At Oxus, we help institutions accelerate innovation by improving productivity by providing purpose-built apps (eDiary, eConsent, Online recruitment tool including pre-screening tool) that enable orchestration for stakeholders in clinical trials.
DATA MANAGEMENT
We offer an end-to-end Clinical Data Management solution including rapid database (CRFs) design, system validation, real-time data cleaning, query management and resolution, effective external vendor data management, integrated clinical data sources, database lock, and clean.
STRATEGIC IT/DATA CONSULTANCY
Our experienced team of Software Engineers and consultants can advise on EDC systems, procurement and implementation, infrastructure and system design, staffing structures, management and leadership.
DATA PROTECTION AND GOVERANCE
Our team has worked with national and international institutions supporting them compliance with GDPR and other complex legislative landscapes including DPIA, DSPT and DTAC.
REGULATION AND AUDIT (MHRA, FDA, EMA)
Oxus’s team of experienced QA, regulatory and clinical research professionals, dedicated to providing high quality, practical, responsive and cost-effective services to support institutions and pharmaceutical companies with early and late stages of clinical trials.
SYSTEM VALIDATION
Our experienced team of Software Engineers and consultants can provide guidance and training on the principle of system validation (e.g. REDCap, OpenClinca), regulatory compliant system documentation, validation plans and risk-based approaches.
CLINICAL TRIALS APPS
At Oxus, we help institutions accelerate innovation by improving productivity by providing purpose-built apps (eDiary, eConsent, Online recruitment tool including pre-screening tool) that enable orchestration for stakeholders in clinical trials.
CLINICAL TRIALS TOOLS
The COVID-19 pandemic made it clear that we need new ways of conducting clinical trials through robust technology, which place less burden on participants. Oxus can provide you with the listed application to make this possible.
1.
E-DIARY
Participants are more likely to be engaged in clinical trials and other research studies when the process is transparent. They can understand their role in the research that leads to advancements in their conditions’ treatment or diagnosis. The ability to easily submit their data is critical. Oxus has developed processes and technology to support collecting and analysing these participant-reported data through its eDiary app.
2.
E-CONSENT
Before COVID-19 and during COVID-19, obtaining informed consent in clinical trials required a complex, in-person process that often took hours. The administrative work and expense of maintaining paper records could be a severe drain on limited study resources. The expert team at Oxus can advise/provide with an e-consent application that meets the regulatory requirements and key considerations for ethics board approval.
3.
RECRUITMENT TOOL
Recruiting and retaining participants in clinical trials is challenging, costly and time-consuming. With years of experience, we have to build a recruitment tool that improves the recruitment process, including online screening.
4.
REAL-TIME QC & DATA CLEANING
We understand that one significant role of data management in clinical trials is to ensure that the data is valid, auditable and accurate. It is essential to provide reliable data for statistical analysis; if this is not done, the data integrity can be compromised, and the outcome of the study can change.
GLOBAL PARTNERS
