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    A pharmaceutical laboratory producing medications, adhering to Good Clinical Practice (GCP) guidelines. The lab features advanced equipment and a qualified team of auditors who ensure quality through systematic audits, verification of standard operating procedures, and assessment of clinical trials at various stages of development.

    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. Good Laboratory Practice audit system is a highly useful tool in the selection of subcontractors.

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      Please be advised that the administrator of personal data entered in the above form is SciencePharma Sp. z o.o. with its registered office in Warsaw, Chełmska 30/34. These data are processed in order to receive incoming correspondence and respond to it. Providing personal data is voluntary, but necessary to send the form. Each person has the right to access their data and correct it.

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