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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.

    良好实验室规范（GLP）GLP

    为了确保非临床研究的质量以及临床试验中的生物分析测定，所有提到的研究都应按照《药物非临床研究质量管理规范》（GLP）的原则进行。

    SciencePharma拥有一支经验丰富的审计团队，他们在进行非临床体外和体内研究方面拥有广泛的知识，并使用色谱和生物方法对临床试验参与者的样本进行分析。

    我们提供质量体系审计，以符合GLP建议，在此期间，我们不仅验证标准操作程序和相关文件，还验证组织本身、员工资格、研究方式和记录保存。良好实验室规范审计系统是选择分包商的一个非常有用的工具。

    See more podlinkować do chińskiej wersji GLP remote and on site

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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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