Accel Research Sites is a multi-therapeutic network of clinical research sites dedicated to the expert delivery of treatment options to patients and providers. We partner with the most innovative and significant pharmaceutical, biotechnology, and medical device companies in the world to advance healthcare and wellness in the communities we serve.
Accelerated Enrollment Solutions (AES) helps biopharmaceutical companies overcome patient recruitment and research site challenges to deliver greater speed, certainty, and control to clinical trial delivery.
Through the combination of a powerful patient recruiting solution and more than 160 owned and partnered clinical research sites throughout the world, AES provides a single global source for clinical trial sites and patients that delivers centralized control, consistent operations and quality worldwide, and more patients from fewer sites in less time.
AES is a business of PPD, a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services.
Our vision is to conduct clinical trials better and more cost effectively than anyone else. We accomplish this by working with our clients to not only deliver the clinical trial effectively, on time and within budget, but also by leveraging our in-depth expertise to ensure the clinical trial is properly designed.
We believe there is increasing need for innovation, creativity and scientific expertise in clinical research, characteristics often synonymous with small Biopharma and hence, though we are proud to have a number of the world’s largest pharmaceutical companies as our clients, greater than 80% of our client portfolio is small Biopharma.
ACLIRES has performed trials for an international array of biotech companies as well as for some of the largest global pharmaceutical companies. With our broad access to patients and expertise, our aim is to rapidly initiate our client’s studies, even when a very special patient population is required.
Our services include:
- Early Phase Studies
- Late Phase Studies
- Regulatory Affairs
- Site Selection
- Scientific Services/Medical Writing
- Quality Management
Advanced Clinical Research, Inc. (ACR) is a progressive, community-based network of clinical research sites. Based in Utah and Idaho, ACR has been in operation since 1984. ACR's commitment to high ethical standards and premier service ensures our study volunteers have a rewarding and worthwhile experience while contributing to the advancement of medical science. ACR's highly trained staff of research professionals ensures that research projects are initiated with quick study start-up, fast enrollment, and high-quality data collection.
As consultants for the pharmaceutical, biotech and device industries we know that teams assembled around product development and clinical trials need more than a competent project manager and top technology to be successful at delivering according to plan.
To be successful, project teams in the health industry need a leader, with a strong medical and industry background, that will inspire, coordinate their efforts, and act as a single point of contact or reference for all involved; sponsors, sites, CROs, data & safety monitoring committee, clinical endpoint committee, special labs, IRB, FDA.
Anabase, founded by two MDs with both clinical practice and industry experience, provides independent, dedicated, hands on, medical and regulatory guidance to your product development and clinical trial projects.