ACRP and ACRES create strategic alliance to improve conduct of clinical research
August 19, 2013 Tweet
The Association of Clinical Research Professionals (ACRP) and the Alliance for Clinical Research Excellence and Safety (ACRES) have joined forces to address critical challenges facing the clinical research enterprise globally and to improve medical product development and delivery worldwide.
This strategic alliance creates a practical mechanism for collaboration among ACRP's clinical research professionals and ACRES' global stakeholders in the pharmaceutical, biotechnology and medical device fields.
Under the terms of their alliance agreement, the two non-profit organizations will focus on 3 issues: the professional development, training and credentialing of clinical research professionals globally, an expertise of ACRP; the registration and accreditation of ACRP-affiliated sites as members of the ACRES Global Network; and tools and services to enhance safety, quality, compliance, productivity and sustainability of research sites worldwide. All projects will involve the multiple stakeholders engaged in the clinical research enterprise.
In announcing ACRP's strategic alliance with ACRES, Gary Shangold, MD, CPI, Chair of ACRP's Association Board of Trustees, noted that "it is difficult to imagine a more natural partnership than one between ACRP and ACRES— we share a common vision based upon a shared belief that clinical research should be done right, by professionals, wherever in the world it is done. ACRP's mission is to provide global leadership to promote integrity and excellence for the clinical research profession. ACRP believes that the ACRES Global Network will provide an opportunity for such professional sites to distinguish themselves through their commitment to quality and safety of research participants. "
ACRES President and Chief Executive Officer, Greg Koski, MD, PhD, a former member of the ACRP Board agreed, emphasizing the value of a global systems approach for enhancing safety, quality and efficiency of the clinical research process. "Clinical research is the essential pathway for getting safe and effective medical products to the people of the world, to improve health, productivity andquality of life. A world-wide system for clinical research will enhance safety and drive quality, standardization, inter-operability, efficiency and excellence across the entire clinical research endeavor for the benefit of all stakeholders. Our goal is to work collaboratively with the multi-stakeholder community to build a network-system that recognizes and rewards excellence in the research process while enabling the timely development of medical products. ACRP will be a superb ally in this effort."
For more than 30 years, ACRP, a non-profit professional association, has been dedicated to promoting excellence in clinical research through the development of competency based education, training and certification of clinical research professionals. Today, ACRP offers the only NationalCommission for Certifying Agencies (NCCA) accredited professional Certification Program for members of the clinical research team, including clinical research monitors(CRAs), clinical research coordinators(CRCs)and investigators(PIs). ACRP's Code of Ethics and Professional Conduct sets a standard to which clinical research professionals aspire.
ACRES is a non-profit organization operating collaboratively in the public interest to build a global system for clinical research. At the heart of this system will be a network of accredited clinical research sites with professionally certified research teams.
More information about ACRP, a non-profit organization based in Alexandria, Virginia, and its programs and services is available at www.acrpnet.org.
Leveraging global expertise to create a connected world of clinical research that is safer, better, faster
ACRES is a non-profit organization working collaboratively reshape the world of global clinical research by leveraging the expertise and investments of stakeholders world-wide to build and maintain a shared global system for clinical trials that are responsibly conducted according to the highest standards of safety, quality and efficiency; and by aligning ethical principles with good business practices to facilitate responsible biomedical product development and health research to benefit all people of the world.
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