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KLR provides our clients with the most effective regulatory assessment and strategy for all stages of medical product development. We have an experienced expert team and can provide a more efficient path through the complex regulatory challenges. Our 3 senior experts have up to more than 10 years of experience working in the regulatory departments of leading global pharmaceutical companies. To make the best use of your time, prior to your application submission we will make an effective plan and careful preparation. Our regulatory specialists and medical writers produce quality documents that are compliant with ICH guidelines and local regulatory requirements. KLR provides regulatory services collecting, analyzing and communicating the latest developments in clinical trials regulatory developments and requirements. It also provides consultation on regulatory compliance issues and helps identify and support regulatory compliance training needs. Our target is to build on our existing experience and success to increase our reputation for high-quality services.
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