Who we are

Welcome to Harmony Pharma Group

We proudly maintain strong partnerships across the pharmaceutical, biotech and contract development manufacturing organizations (CDMOs), welcoming the opportunity to lead domestic and global projects for CMC development teams. We are flexible, creative and determined in the pursuit of harmony for our clients.

At Harmony Pharma, we specialize in propelling small biotech and pharmaceutical firms forward in their journey towards Small Molecule Drug Product and Antibody Drug Conjugate (ADC) development, CMC Regulatory, Clinical Packaging, and Commercial Readiness. Our meticulously designed processes and systems are tailored to arm your CMC leaders with the essential tools for success, ensuring consistent and predictable results. With a highly skilled team of consultants at your service, we are committed to nurturing your growth while adhering to the highest quality standards. We are here to significantly expedite your First In Human (FIH) timeline, provide continual support for your clinical supply needs, and assist in regulatory filing and quality compliance. Engage with us today and discover how our dedicated consultancy can drive your growth and uphold superior quality in every facet of your endeavors.

Passionate CMC Experts

We help small biotech and pharmaceutical company develop a Chemistry Manufacturing and Controls (CMC) clinical and commercial strategy for their Small Molecule or Antibody Drug Conjugate. We have deep expertise in Small Molecule Drug Product development, CMC Regulatory, Clinical Packaging and Commercial Readiness needs. We are currently partnering with companies to accelerate their ADC development from bench to bedside. Our process and system is designed to empower your CMC leaders with the tools needed to succeed and provide them with consistent predictable results. Talk to us today about how our highly skilled team of consultants can support your growth with utmost quality to meet or exceed your First In Human (FIH) timeline, support ongoing clinical supply needs, regulatory filing and quality compliance.

Our Analytical Approach

Our service includes a comprehensive consult to help identify gaps and opportunities, and results in a comprehensive report that includes a project plan with timelines and cost analysis. Our individualized plans are made up of quality services that will help you get there quickly and smoothly.

Success starts with utmost Quality and Speed in

Technical Product Development (PD)
of Small Molecule or ADC

Global CMC
Regulatory Affairs (RA)

Quality Assurance (QA)
and Compliance