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To successfully develop new drugs in a timely manner, multinational clinical trials are beginning to access global central lab services. However, harmonized data is necessary to get global approval. To pursue the results with efficiency, high quality service and technology are critical. Therefore, the reliability of the central lab provider is of the utmost importance. Quintiles Central Laboratories provide solutions required for multinational clinical trials.
With largest global network, all Quintiles laboratories are directly managed by Quintiles. From testing kit to sample storage, analysis method and data collection, appropriate management controls are in place. In addition, because instrument and SOP are harmonized in all laboratories, it is possible to directly compare patient data collected in South America and Beijing.
Because all laboratories in the global network are centrally managed, clients can use the service in the region where clinical trial is performed. Quintiles is establishing excellent relationships with regulatory agencies and courier companies according to the local language and practice. As a result, you can achieve efficient analysis and early database lock using globally harmonized data. This will also ensure you can make decisions much faster based on the reliable information.
Quintiles Central Laboratories own the facilities in United States, Europe, South America, India, China, Singapore and Japan. These are centrally managed as a network. Also, in Argentina and Brazil, our affiliate laboratory is supporting sites.
Quintiles Central Laboratories is establishing a network of expert groups. Each team is responding to the needs specific to a therapeutic area.
In collaboration with you, we help establish the database that is most appropriate for the protocol and needs. In addition, the project is initiated after we completely understand all processes including protocol preparation, communication and issue resolution. By doing so, it is unnecessary to learn client processes one-by-one, which allows us to save you time during the most important time in a clinical trial: its initiation.