<ruby id="15vlr"></ruby><noframes id="15vlr">

        <address id="15vlr"><form id="15vlr"><th id="15vlr"></th></form></address>

        <address id="15vlr"></address>

        Home About Us Resource News & Events Sites
        Building Blocks

        Analytical Development & Quality Control

        At PharmaBlock, our analytical development and QC teams provide full spectrum services in analytical development, method validation, release testing and stability study from drug substance to drug product.


        ?  Analytical method development, validation and transfer in comply with ICH guidelines

        ?  In process control and release testing in comply with GMP requirement

        ?  Forced degradation (stress) study for the detection of impurities or degradation products

        ?  Stability studies under varied temperatures and humilities per ICH guidelines

        ?  Impurity isolation and identification using prep-HPLC, LC-MS, GC-MS, FT-IR and NMR spectroscopy

        ?  Genotoxic and elemental impurity method development and validation

        ?  Reference standards characterization and qualification

        ?  Microbial limit testing

        ? 可以免费观看的av毛片 - 视频 - 在线观看 - 影视资讯 -心晴网