Syner-G BioPharma Group is a leading CMC and Regulatory Affairs solutions provider for the biopharmaceutical industry, specializing in Chemistry, Manufacturing, and Controls (CMC) Regulatory Services, Technical Development, and Quality GxP Compliance. With a proven legacy of successfully working with small, medium, and large BioPharma clients, their team of experts offers in-depth expertise across various therapeutic areas and all phases of development, providing clear and concise documents that meet both scientific and regulatory requirements.
Driven by a philosophy of doing it right the first time, Syner-G is dedicated to patient safety and regulatory compliance, offering science-based, risk-based, and phase-appropriate solutions to expedite drug development and sustain the commercial supply chain post-approval. Their integrated CMC 360 and Regulatory Affairs business units ensure that the solutions provided adhere to scientific standards and regulatory requirements, while their team's collective knowledge and critical thinking abilities set them apart in the industry.
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