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Global ServicesWith human lives at stake, trust the proven expertsFor more than 40 years, WIRB has been at the forefront of protecting the rights and welfare of human subjects. With our unparalleled regulatory insight and experience, WIRB can manage these complexities and ensure your research gets a thorough review quickly.Learn more about our IRB Services.Clinical Pharmacology Unit ReviewThe clock is always ticking for clinical pharmacology research. And, multi-site coordination, we deliver unparalleled review quality to ensure your research withstands scrutiny around the world.Learn more about the WIRB advantage.IRB ServicesRegulatory requirements, institutional needs- there are many complexities that can slow down research. We provide in-depth regulatory expertise to support your development of research protocols and documentation.We offer customized training and consulting about human protections, addressing research design through implementation. WIRB's Clinical Pharmacology Unit Services division is set up to respond quickly for fast and thorough review of Phase I studies and beyond.Learn more about CPUS reviews.Institutional Biosafety CommitteeSafe storage, handling, and disposal of gene-modified, biohazardous materials-these issues are among the many challenges for investigators and sponsors of research involving recombinant DNA.
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