Teaming Together To Extend Patients Lives
We are a strategic Contract Research Organization (CRO) running multiple clinical trials in community oncology sites throughout the US. Uniquely focused on community-based hematology & oncology research sites, we provide real-world experience, data and outcomes that lead to improved clinical utility of cancer therapies, improving the lives of cancer patients.
Our full suite of services include expert dedicated project teams, medical writing, data management, analysis and reporting as well as regulatory submissions. Nationally recognized research oncologists and Key Opinion Leaders in the oncology field work in parallel with our senior level clinical research teams. We have an excellent track record of short start-up times and adherence to enrollment and completion timelines.
Our history of client satisfaction and success is the best testimony of our commitment to our clients.
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.
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
VetPharm, Inc. is a full-service contract research organization (CRO) dedicated exclusively to animal health. It offers a complete menu of pilot/pivotal/post-marketing clinical trial support services, including protocol development, data form design, investigator recruitment, site qualification, enrollment enhancement, study administration, ICH-GCP training, site monitoring, data management, statistical analysis, medical writing, and regulatory support to pharmaceutical, biotechnical, nutraceutical, nutrition, and device companies in the United States and Europe. VetPharm employs a comprehensive study management system and a consortium of study-ready investigators which facilitate rapid study initiation, accelerated enrollment, and superior results to meet sponsors' critical timelines.
VetPharm has broad clinical trial experience across all therapeutic areas which enables it to undertake virtually any trial and complete it quickly, efficiently, and accurately. VetPharm's investigator consortium includes board-certified specialists in the following disciplines: Behavior, Cardiology, Dentistry, Dermatology, Endocrinology, Gastroenterology, Immunology, Internal Medicine, Neurology, Oncology, Ophthalmology, Radiology, Surgery, Theriogenology, and Urology.
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
Allphase Clinical Research is a full-service clinical development company providing clinical trial management services, including regulatory affairs, project management, clinical monitoring, data management, quality assurance auditing, drug safety, and medical writing. Allphase provides Phase I to IV support throughout a wide range of therapeutic areas, with a predominant focus in oncology, CNS, and critical care diseases.
Allphase provides integrative and strategic clinical trial services that allow our international partners to realize the advantages of conducting clinical trails in North America, while reinforcing therir global development cpabilities.