The Clinical and Regulatory Affairs Team at Neurim Pharmaceuticals Ltd is responsible for designing, managing, and overseeing clinical trials to ensure the safety and efficacy of new drugs. They also handle regulatory submissions and compliance, ensuring that all products meet the necessary legal and ethical standards for approval and commercialization in various markets. This team plays a critical role in advancing Neurim’s R&D pipeline, with a focus on treating conditions such as insomnia, Alzheimer’s dementia, and sleep apnea.
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