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About AppHIA Clinical Research
Who We Are
Apphia Clinical Research is a research consulting firm, based out of NC. We provide consulting and clinical research support to research sites, desiring to increase their footprint in the research industry. We offer a breadth of services, allowing us to cater to a diverse range of site needs. Currently we provide services to Upper Central South Carolina, North Carolina and the Outer Piedmont Province of Virginia.
Our services include:
- Transitioning existing practices or patient care facilities into clinical research sites
- Identify ethically and scientifically sound trials that align with therapeutic expertise
- Training of clinical staff to perform respective tasks
- Regulatory submissions and readiness
- Quality Assurance of clinical trials
- Ensures that all clinical trials are approved by the Institutional Review Board (IRB) or Independent Ethics Committee (IEC)
- Design and Lay-Out
- Start-Up Services
- On-site and Remote Monitoring Support
Our Philosophy
Our philosophy is simple. Always do the right things, for the right reasons. This is our commitment to ensure ethical conduct, maintain integrity and serve with a sense of purpose.
Vision
Apphia's vision is to diversify and streamline clinical research activities to ensure the success and efficiency of research processes. Apphia plays an essential role in the clinical research ecosystem by facilitating the connection between patient care facilities and Sponsors. Our methodical approach is essential in maintaining high standards of quality throughout research. We share knowledge to ensure that each research site operates efficiently while demonstrating good clinical practices.
Our Team
Our team is diversified and possesses a wealth of experience and expertise in the field of clinical research. With over 20 years of extensive experience and a diverse range of therapeutic specialties, we are well-positioned to provide valuable insights and contribute to the success of clinical research sites. We stay up to date on industry related trainings, certifications and trends. This dedication positions our team as a valuable resource. Keeping abreast of industry developments is crucial for adapting to the evolution of research and providing the best possible support to clinical research sites.
Methodology
Apphia seeks to be the consulting service of choice and recognized for our professional, high-quality services. We use a rigorous and systematic approach to clinical trials. Our methodology is designed to ensure that our projects are ethically responsible, GCP compliant and conducted with safety of the patient and quality in mind.
People... Ethics... Morals
At Apphia, our core values are unambiguous. We are patient centered and place Humanity FIRST! We prioritize placing a high emphasis on moral and doing the right things ALWAYS. Our organization aims to ensure the rights, safety and well-being of every patient. We take pride in ensuring that the clinical trials chosen for your site are ethically and scientifically sound. In identifying potential trials that coincide with your therapeutic expertise we promise that trials will be chosen under the guise of benefits outweighing the risk for patients. Apphia Clinical Research adheres to Good Clinical Practice (GCP). GCP aids in developing compliant trial design, conduct, monitoring, analyzing, and reporting. We are committed in ensuring your clinical trials will meet international ethical and scientific quality standards.