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We understand that effective program management is critical to success. That is why your project will receive an experienced multi-disciplinary Project Team, selected to meet the criteria of your specific program, who are experienced in the therapeutic indications. MetaClin’s research staff includes a wide variety of disciplines, such as; Project Managers, CRAs, and Clinical Coordinators with a great deal of quality experience in the management of clinical trials from Phase I through to Phase IV. Whatever the challenge in the clinical phase of a product’s development, MetaClin has assisted a distinguished list of pharmaceutical and biotech companies in completing very successful studies, leading to marketing authorization. Our Clinical Development Services include: - Project Management
- Clinical Operations
- Clinical Trial Materials
- Phase I-IV Clinical Trial Site
MetaClin assembles a project management team uniquely qualified for each project. A manager, dedicated to the project for its duration, heads the team and oversees all functions to assure ongoing compliance with procedures and goals. To ensure successful completion of all projects, the Project Managers are responsible for fielding questions, monitoring accurate implementation of instructions, and resolving any study-related issues that may arise. Meticulous planning, timely implementation, and precise execution of all project responsibilities, combined with time-tested tracking and reporting systems, allow MetaClin’s staff to claim an impressive history of completing projects on time and on budget. Clinical Development
Monitoring services at MetaClin are considered an integral and critical part of the data management process. We have a network of Clinical Research Associates (CRAs) who are trained in various therapeutic areas. Careful consideration is given to our CRAs therapeutic expertise and training requirements. Along with GCP, ICH and company SOP training, the CRAs undergo client specific program training and individual therapeutic area training offered throughout the year. Pre-study involvement and continuous interaction between CRAs and data management staff ensure accurate and consistent case report form completion, resulting in a significant reduction in time spent on queries and database clean-up. The staffing process is dependent upon client needs and expectations; our experienced team will be project specific and may work on two to four projects to provide efficiencies in travel time and accessibility to the sites. TrialQuest
TrialQuest-data gathering services in the field of healthcare clinical trials via the internet in Class 042 Download a brochure>
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