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Why Choose Us?

Quality Data Output

Quality is paramount in clinical trials, as it ensures that the data collected is reliable and that the trial results are meaningful. However, achieving quality can be challenging, given the many factors that can impact the success of a trial. At agile we make sure the data will be coming out in quality way which is accepted internationally Clinical Data Interchange Standards Consortium (CDISC) & Study Data Tabulation Model (SDTM).

Code Capability And Benefits Of Cost Affective Clinical Trails

Clinical trials evaluating medicines, medical devices, and procedures now commonly assess the economic value of these interventions. The growing number of prospective clinical/economic trials reflects both widespread interest in economic information for new technologies and the regulatory and reimbursement requirements of many countries that now consider evidence of economic value along with clinical efficacy. Agile makes decision in this for cost-effective demand evidence of economic value for health care interventions, conducting high-quality economic analyses alongside clinical studies is desirable because they broaden the scope of information available on a particular intervention, and can efficiently provide timely information with high internal and, when designed and analyzed properly, reasonable external validity.

Trusted By Sponsor & CRO's Loved By Sites

Working with a Agile can offer many benefits to clinical research teams, including:Faster patient recruitment – Agile SMOs leverage networks of qualified patient pools and faster follow-up to recruit and retain patients more efficiently than in-house teams. Improved data management – With the technological infrastructure and data handling processes in place to manage both clinical and regulatory data, Agile SMOs limit delays that can sometimes crop up with study and regulatory data addressing inefficiencies. Better focus for research teams – A common pitfall that clinical research teams can face is spending more time cleaning data than analyzing data. With the grunt work outsourced to Agile SMOs, research teams have more time to analyze meaningful data. Shorter study timelines and lower costs – Agile SMOs provide end-to-end clinical trial-related services, from setup to monitoring, compliance activities, and closeout, to shorten clinical research timelines and stick to budgets.

Our advanced model - The FDA and other relevant regulatory authorities require intricate and accurate data for approvals. Agile CROs work within clinical compliance on a daily basis, which gives them intricate knowledge of regulatory requirements and audits such as Good Clinical Practice (GCP) audits or Good Laboratory Practice (GLP) audits with continous regulatory training programs. Agile CROs work with Agile hiring SOP's to optimize audit results through careful review of any previous issues, close inspection of infrastructure, and adherence to current protocols.

Project Management

While our team brings important experience and knowledge, we know that each patient is the expert in their own life.

Best Clinical Research Facility

While our team brings important experience and knowledge, we know that each patient is the expert in their own life.

Expertise Certified Professionals

While our team brings important experience and knowledge, we know that each patient is the expert in their own life.