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    GLP

    In order to ensure the quality of non-clinical studies as well as bioanalytical assays in clinical trials all the mentioned studies should be conducted in accordance with the principles of Good Laboratory Practice (GLP).

    SciencePharma has an experienced team of auditors having broad knowledge in conducting of non-clinical in vitro and in vivo studies, as well as in performing analyses of samples taken from participants in clinical trials by using of both chromatographic and biological methods.

    We offer auditing of quality systems for compliance with GLP recommendations, during which standard operating procedures and related documents are verified but also the organization itself, qualifications of staff, the way of studies conducting and records keeping. GLP audit system is a highly useful tool in the selection of subcontractors.

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