Why Choose ABRI
ABRI is an independent and neutral source of bio-products, which is of an eminent service to its customers. When a customer has the need for a collection of rare, highly characterized biological samples, ABRI is the one provider that is able to constantly deliver high quality samples in a timely and efficient manner and within full regulatory compliance
Support .
Providing support to pharmaceutical sponsors, clinical research organizations for the conduction of Clinical Trials throughout multiple geographies.
Consult .
Consulting Service to Evaluate Protocols, Investigator Brochure, Electronic Case Forms, IWRS/IVRS.
Provide .
Providing Audit support during state and/or federal inspections primarily FDA and CDC.
Practice .
ABRI clinical trial management programs will be coordinated though a staff of leading clinical pharmacologists and doctoral level research scientists.
Initial Phase (screening)
At ABRI, we are actively looking for individuals just like you to help answer important questions about a variety of health conditions. You can learn more about study participation for research studies below. Clinical Research participants help the discovery and implementation of important medical innovations to include genetics, drugs, clinical techniques, and diagnostic tools. Becoming a participant will help future generations to include family, friends, and neighbors.
Initial Phase (screening)
- A dedicated ABRI staff member will review the different diagnosis and match each individual potential participant to a study.
- Before and during the screening visit, patients wili be invited to join the study and provide informed consent. During the process, patients will receive information on the purpose of the study, treatment choices, what phase is the study testing, how long will the study last, and what kind of testing will be required.
- Patients will also receive information on the pharmaceutical company, health monitoring, participation stipend and transportation offered.
- Understand that study participation is completely volunteer, private health and demographic information will be always protected.
Participation
- ABRI physicians and clinical team will monitor your health at all times.
- Patients will have the chance of receiving free medications for their conditions. In double blind studies, participant often receive a rescue therapy as well.
- During the treatment phase, patients will visit the center periodically.
- Several procedures will be part of the study and ABRI will offer them to the patients free of charge. This includes:
- Patient can continue to see their own doctors during study participation.
Outcome
- Patient will receive information when a study is getting to the end. Several studies offer Open Label Extensions which mean, the participant will continue to receive the actual medication for an extended period of time.
- During the extension phase, patients will continue to be seen by an ABRI medical professional and will be offered several of the ancillary examinations completed in the treatment phase.
- During the treatment phase, patients will visit the center periodically.
- Study results and outcome are often share with the public via newsletters, internet infomercials and/or pharma company press release.