Accelerated Enrollment Solutions

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
- Recruitment
- Regulatory Affairs
- Monitoring
- Site Selection
- Scientific Services/Medical Writing
- Consulting
- Quality Management

For more than 35 years, BBK Worldwide (BBK) has been instrumental in the development and evolution of the patient recruitment industry. With a commitment to innovate, the company pushes the industry forward with the development of game-changing tools and technologies that enroll and engage patients in clinical trials. BBK was founded by Joan F. Bachenheimer and Bonnie A. Brescia, inspired by a shared commitment to advocate for patients and patient-centric care.

BBK’s suite of solutions address the needs of today’s clinical trial sponsors, with a focus on products and services that educate consumers, engage participants, unburden sites, and support sponsors. Committed to transforming the patient experience, the company’s end-to-end solutions support the entire clinical trial journey.

Cohortias is the SCIENCE CRO for Latin America, merging the high efficiency standards required for CLINICAL RESEARCH with tight and unbiased scientific rigor characteristic of academia. Through our extensive academic liaisons in Latin America we have built a broad and highly reputable network of sites which can access patients in a timely manner and operate with the highest quality standards. This ensures an easier entrance for products into the market.

We define ourselves as a unique team, capable of blending our academic background with a global business mindset to bring the highest standard of quality and operational excellence into clinical research for Latin America.

Cohortias offers specialized staff to perform all aspects of site management and clinical research monitoring throughout Latin America, and we can scale to facilitate all the required clinical site management services.

Our academic network offers access to the leading investigators in their respective therapeutic areas in Latin America, and peer-to-peer management to guarantee the highest recruitment and retention.

We provide our CRO Services with offices in:

- Mexico
- Brazil
- Colombia
- Argentina

We believe in opening the opportunity of Clinical trials for the patient population in Latin America, and thus leveraging the transformation of healthcare in the region, through better access for care and better care for each one.

Founded in 1986, Grayline Research Center is a full-service contract research site dedicated to providing high quality clinical trials management and support to pharmaceutical companies for Phase II – IV clinical trials under FDA review.

Today, Grayline is recognized as a premiere clinical trial research facility. The company and its staff bring to each clinical trial a formidable body of experience and expertise. That collective experience covers a wide range of research designs, targeted illnesses, patient populations, and recruitment strategies.

Dedicated to meeting and exceeding the objectives and requirements of the pharmaceutical industry, Grayline Research Center adheres to the highest standards and processes. Our team is well versed in the regulatory requirements and we are committed to excellence.

ICTS provides innovative, creative, and targeted solutions for all aspects of the clinical trial process from pre-trial preparation to patient recruitment to retention and compliance and pre-launch transition. Our methods lead to increased quality, higher compliance, and more highly educated sites and patients. We’ve worked on over 500 protocols and have significant experience all therapeutic areas.

Our programs are always developed exclusively to the requirements of the protocol and the study team and we have the flexibility to work within budgets as a niche or full service provider.

You can also take a look at our website which has some more in depth information.