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General Inquires |
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At Qualia we know that the solution to successful outsourcing is finding the right vendors who can deliver quality results and premium service at a good price. our proven global network of facilities and partners offers clients exactly that, with access to a complete suite of premium clinical research services.
Our network creates a compelling value proposition for the pharmaceutical, biotechnology, and generic industries by providing access to streamlined drug development services with an unprecedented emphasis on quality and efficiency. Qualia can achieve synchronized scheduling to minimize downtime in the research process. Clients are able to sign a single contract and utilize Qualia as a complete resource.
Clinical Research
Qualia offers Phase I-IV clinical research options at locations around the globe. We can facilitate any type of study, using our experience as the foundation for providing innovative service. Qualia provides rapid recruitment, timely results, and the absolute premium in customer service. We conduct trials in state-of-the-art facilities, fully equipped to handle virtually any study. Our team of seasoned industry professionals ensure that accurate data is delivered when promised and exactly as the client requests. Whether clients need normal and healthy volunteers or special populations, Qualia provides a single resource for every situation.
Lab & Bioanalytical
Qualia maintains a partnership with one of the nation’s leading bioanalytical laboratories, Tandem Labs. Tandem has been supporting pharmaceutical and biotechnology companies with its drug discovery and development programs since 1992. This Qualia partner offers advanced mass spectrometry, immunoanalytical support, and pharmacokinetics and pharmacodynamics (PK/PD) services. With multiple facilities in the United States, Tandem Labs is equipped to support both large (over 50,000 samples) and small (fewer than 100 samples) studies. Our close partnership yields a seamless relationship and reliable data transfer.
Data Management
Qualia employs a highly trained staff proficient in statistics, programming, database design, and GCPs. Our team is well-trained in the regulatory requirements governing these sectors and is well versed in meeting stipulated audit standards for all data handling, analysis, and report writing. Qualia has the expertise to manage and analyze data for Phase I, II, III, and IV clinical trials. From the CRF to final report, we use only the most efficient and acceptable processes that meet audit standards. Qualia provides databases designed according to statistical and clinical needs, database programming using SAS, data entry, data validations, query generation and management, and report generation.
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