Syner G Biopharma

Pharmaceutical Manufacturing · 201 Employees
Phone Number: info@synergbiopharma.com
Email Address: info@synergbiopharma.com
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About
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 360™. 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 along the ever-changing maze of regulatory filing pathways, to a position of full compliance, and high quality. Our expertise spans small molecules, peptides, oligonucleotides, biologics, monoclonal antibodies, antibody-drug conjugates, and cell and gene therapy products.
Year Founded
2007
Social Media
Linkedin
Industry
Pharmaceutical Manufacturing
HQ Location
100 Pennsylvania Avenue Framingham, MA 01701, US
Keywords
cGMP SolutionsRegulatory Science for Pharm DevelopmentCMC Formulation DevelopmentPost-Approval CMCMedical Writing ServicesBiologicsCell and GeneProject ManagementRegulatory ServicesCMC
Location
4
  • 100 Pennsylvania Avenue Framingham, MA 01701, US
  • 79 T.W. Alexander Drive Building 4401, Suite 101 Research Triangle Park, NC 27709, US
  • P. No. 15, W-Block, 2nd Floor North Main Road Anna Nagar West Extension Chennai, 600 101, IN
  • 6000 Spine Road Suite, 201 Boulder, CO 80301, US

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