For 35+ years, Advocates for Human Potential, Inc. (AHP) has focused our people, passion, and expertise on creating practical solutions to improve health and human services systems of care and business operations. Through hands-on research and evaluation, training and technical assistance, and professional consulting, AHP assists organizations of all sizes in achieving our collective goal of helping our most vulnerable populations lead full and productive lives. Every day we work to develop “real-world solutions for systems change” through our areas of expertise in addictions & substance abuse, behavioral health policy, criminal justice, health care reform, housing & homelessness, mental health, population health management, recovery supports, veterans, and workforce development. AHP applies best practices, many of which we have helped to shape, to improve your programs and business practices. We work with you at the front lines of change—where theory meets real people and programs—with practical approaches and concrete solutions using research and evaluation, technical assistance, and business consultation. We serve clients representing a broad range of federal, state, local, and community-based agencies, as well as commercial organizations. Our nationally known experts—teachers and business leaders, researchers, innovators, and change-makers—bring their passion and commitment to transforming knowledge and experience into practical strategies and results. We deliver on our promises, and beyond that, we care about what comes next—your future and your outcomes as a result of our work together. With every engagement, our focus is on change and improvement, serving you and your organization and ultimately improving health for individuals and populations. AHP is headquartered in Sudbury, MA with offices in Chicago, IL; Pasadena, CA; and numerous satellite offices throughout the U.S. Visit http://www.ahpnet.com.

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.