The Regulatory Affairs and Project Management team at ACIC Pharmaceuticals Inc. ensures that all products comply with regulatory standards and guidelines while managing the lifecycle of pharmaceutical projects. This team handles the submission of regulatory documents, oversees quality assurance procedures to maintain cGMP compliance, and coordinates project timelines and deliverables to achieve successful product approval and market launch. They bridge the gap between regulatory requirements and project execution, ensuring seamless and efficient operations from molecule development to market distribution.
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