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Massachusetts Biotechnology Council

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Syner-G BioPharma Group

Associate Industry | Clinical & Regulatory Strategic Consulting
Southborough, MA 508-460-9700 Website LinkedIn

Overview

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.

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News

Syner-G BioPharma Group Acquires Impact; Expands Services for Biotech and Pharma Companies

Feb 01, 2022

Posted by Syner-G BioPharma Group

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Massachusetts Biotechnology Council

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Cambridge, MA 02139
617.674.5100

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