Syner-G

Syner-G Pharma Consulting provides comprehensive customized CMC regulatory services for biopharmaceutical companies. At Syner-G Pharma Consulting, our sole focus is Chemistry, Manufacturing, and Controls (CMC). We offer a full suite of CMC solutions (CMC-360) in the following three core areas: Regulatory Affairs, Drug Development, and QA/cGMP Compliance. We fully recognize that each client and each project is unique, and CMC requirements vary based on several factors such as molecular complexity, formulation, indication, patient population, and development stage. With patient safety and regulatory compliance as primary goals, Syner-G helps design and implement scientifically sound and risk-based, phase-appropriate CMC solutions to rapidly advance your drug during development and/or sustain the post-approval commercial supply chain. Our CMC-360 division operates in an integrated manner to ensure the solutions we provide fully align with scientific standards and regulatory requirements.