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Syner-G BioPharma Group provides in-depth expertise across the three key elements of Chemistry, Manufacturing, and Controls (CMC): Regulatory Services, Technical Development, and Quality/IT. We call this CMC 360TM. We also provide medical writing services, with expertise in authoring a variety of regulatory documents across a wide range of therapeutic areas and in all phases of development. Our regulatory affairs services include the development and implementation of global regulatory strategic plans, regulatory agency meeting support, and electronic submissions to regulatory authorities around the world. We have the skill set and experience to guide your prime asset through any development challenges and...
Cgmp solutions,regulatory science for pharm development,cmc formulation development,post-approval cmc,medical writing services,biologics,cell and gene,project management,regulatory services,and cmc
Syner-g biopharma group operates in the Pharmaceutical manufacturing industry.
Syner-g biopharma group's revenue is 11m - 100m
Syner-g biopharma group has 201 - 500 employees.
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