Continental Clinical 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

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.

Forward Clinical Trials, Inc. is a clinical research facility located in Tampa, Florida, and has been actively involved in clinical research since 2013. Our goal is to provide high-quality and timely data in a professional and ethical manner. Forward Clinical Trials (“FCT”) has successfully executed Phase I through Phase IV clinical trials across multiple areas of dermatology and is expanding into internal medicine and rheumatology.

As a quality-driven site, Forward Clinical Trials has established processes to address the increasing complexities of clinical research.


Efficient Start-Up
We understand the necessity to shorten the trial start-up time at the clinical site. FCT has streamlined its processes to meet the ever-increasing demands of enrollment readiness and prompt subject screening timelines with in-house staff completing regulatory submissions, contract and budget negotiations, training, and trial logistics in a collaborative and systematic manner.


Recruitment and Outreach
Our teams work together to develop pre-screening and recruitment strategies to target the population, decrease enrollment obstacles, and lessen the enrollment time. Efforts are made to identify the most productive and cost-effective method specific to the indication, and a recruitment plan is created. The recruitment plan is continually reviewed throughout the trial, and adjustments are made as needed.


Project Management
Trial execution and logistics are coordinated by experienced management involved in all aspects of the clinical trial. This involves working directly with the Investigator and staff to ensure efficient start-up, QA/QC plans, and recruitment/outreach proposals in a productive manner while acting as a direct liaison to the Sponsor and/or CRO.


Protocol Feasibility
FCT performs an internal feasibility review that includes protocol analysis, patient population, trial logistics, and study design to direct identification and selection of trials where expectations are met or exceeded. We understand the importance of the feasibility process at both the Site and the Sponsor level and remain focused on fostering a partnership between our Site and our Sponsors.


Quality Management
The multi-faceted quality management program is designed to shorten data entry timelines and decrease queries while remaining focused on protocol compliance and subject safety.

We are a full-service contract research organization (CRO) and health research company. Since 1986, we’ve helped pharmaceutical, academic, and federal clients bring innovative drug treatments and other interventions to market. We have supported several federal clients for multiple decades and coordinated hundreds of clinical trials and epidemiological studies in a wide variety of therapeutic areas.

Using a collaborative, “can do” approach, we offer a wide range of clinical services, including study management, observational studies and registries, patient recruitment and site partnerships, regulatory affairs, data management and eClinical solutions, monitoring, safety and pharmacovigilance, statistical support, and quality assurance. Our decades of experience allow us to predict needs, avoid common barriers, and move from a quick startup through each research phase.

Our project managers average 11 years of service, and the majority have worked at Navitas Clinical Research, Inc. for more than 12 years. Their long tenure lends consistency to their project management methods and allows them to draw on extensive institutional and personal memory for every study.

Navitas Clinical Research, Inc. is a wholly owned subsidiary of Navitas, Inc. and a stepdown subsidiary of Navitas Life Sciences Limited. For more information about Navitas Life Sciences, please visit www.navitaslifesciences.com

As one of the most experienced and leading CROs (Contract Research Organization) for over 35 years, McDougall delivers valuable insight to biotech and pharmaceutical clients across all phases of their clinical trials. With timely, accurate data and analytics, we help clients expedite their time-to-market and lower development costs.

McDougall Scientific specializes in Clinical Trial Design services, Statistical Analysis and Clinical Data Management. Known for delivering insights you can trust, we take the time necessary to understand your business requirements, align with your regulatory strategy, and mitigate risks to deliver a vital statistical strategy for the development of your product.

The result: a smooth, efficient, and trusted operation from start to finish. We welcome you to contact us whether you are a company with established assets, or an independent investigator exploring initiating an investigator trial.

Specialties:

Feasibility Assessment, Protocol Development, Study Startup, Project Management, Investigator Initiated Trials, Phase I-IV Trials, Clinical Data Management System, Statistical Services, EDC, Data Management, Supply Management, Randomization, Document Management, Clinical Trial Management, Site Monitoring, Medical Writing, Regulatory Services, Pharmacokinetics, Patient Recruitment,​ Pharmacovigilance, Safety Surveillance, Integrated Safety, Risk-based monitoring