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Let’s Accelerate Your Drug Development, Together
Our experienced team is ready to help you transform your innovative ideas into approved products. We know the ins and outs of CMC development and our goal is to help ensure the safety, purity, potency, and efficacy of the finished drug product from development through commercialization.
Whether you require extra capacity or require our specific expertise, our team and lab can effectively be an extension to your existing operations. Whether you’re kicking off a fresh project in your pipeline or optimizing an existing program, CMC Pharmaceuticals provides integrated solutions across formulation, analytical, stability, and regulatory strategy, through early phases to commercialization.
A Trusted Drug Development Partner
- Decades of combined experience supporting oral solid dose, parenteral, and drug-device combination programs.
- GMP-compliant facilities & FDA Inspected
- Early-stage risk mitigation, helping clients avoid delays and regulatory setbacks
- Customizable solutions tailored to each client’s unique technical and regulatory needs
- Efficient project management and proactive problem-solving.
- Collaborations with academic, biotech, and pharmaceutical partners.
Get In Touch With Our Experts
Fill out the form below and one of our team members will be in touch within 1-2 business days to discuss your project.
Formulation Development
ᴄGMP Lab Services
Analytical Development
Stability Evaluations
Dosage Form Development
Prototype Preparation
“Every successful program begins with a conversation. Let’s discuss how we can reduce risk, accelerate timelines, and make your development program smoother.”
-Dr. Mike Radomsky, President
