![]() O ur GMP manufacturing service provides faster development, higher yield, and better quality, reduced batch-to-batch v ariability, better scalability, and lower production costs. All products have guaranteed stability and batch retention, and are produced in dedicated cleanroom equipment to eliminate potential pollution, and each order is strictly QC and HPLC purified.Īnna said, "From intermediate to API and from chemical drugs to macromolecules, all products are manufactured in compliance with ICH guidelines. The compounds produced by BOC Sciences' s GMP business unit can meet any defined specifications, and customers can fully control the entire process. ![]() Undoubtedly, this move further strengthens BOC Sciences’s ability to provide drug discovery services, including m edicinal c hemistry, custom synthesis, analysis/purification, formulation services. ![]() As Anna Green, the project manager of BOC Sciences, said, “Our optimized cGMP platform is supported by a comprehensive quality plan and quality system, which can help offer a series of products and services for customers who have strictly defined specifications to control the manufacturing process.” The new cGMP manufacturing platform aims to achieve scale flexibility, which can realize routine monitoring of temperature, pressure, humidity, and particle count, and the platform is equipped with ICH Q7 (Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients) cleanrooms, ICH Q8 cleanrooms, and two analytical and functional support laboratories to support product testing. Recently, t he world's leading pharmaceutical product developer and GMP manufacturer, BOC Sciences, announced that it has completed the commissioning of its new GMP platform to produce screening compounds, starting materials, structural units, intermediates, lead compound derivatives, nucleosides, nucleotides, small molecules, active pharmaceutical ingredients (API) and peptides that meet GMP standards.
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