Start Smart, Move Faster
Accelerate your molecule from Preclinical to Commercial
About Hycon
With broad, deep-scale and expertise in small molecule oral dosage development sciences, delivery technologies, and multi-modality manufacturing, Hycon Labs is a preferred Contract Development and Manufacturing Organization (CDMO) partner for orphan drugs, blockbuster drugs, generics, and consumer health brand extensions.Â
Hycon a premier partner in enabling pharmaceutical partners to slash time and costs for oral and topical small molecule product development, launch, and full life-cycle supply for patients around the world.Â
Hycon Labs has unrivaled expertise in formulation development for complex dosage forms. We employ a range of techniques to increase bioavailability or achieve controlled release for even the most challenging APIs. We have experience developing new formulation approaches and optimizing existing products, including oral solid dose (OSD), creams, emulsions, liquids, solutions, films, and suspensions.
KEY ACHIEVEMENTS
SPECIALIZED TECHNOLOGIES
Pick from a variety of dosage forms
Increase efficacy, bioavailability, adherence, and safety.
Avoid Unreliable Partners
Benefits of working with Hycon
Why Hycon is Your Trusted CDMO Partner
Faster Time-to-Market
Cut up to 20 weeks of your early phase and late phase timelines!
Customized Solutions
13+ Oral Technologies and 4+ Integrated Solutions
Scalability
Over 300+ state of the art equipment, 500+ employees, 5 facilities, and 20+ depots that can seamlessly adapt to your evolving needs from early development stages or ready for large-scale production.
Quality Assurance
Ensure compliance with stringent industry standards, reducing your risk guaranteeing product integrity, and timely market entry with products that meet or exceed the highest quality benchmarks.
Expertise and Experience
Our seasoned managment team brings 30+ years of industry knowledge on average, ensuring your programs are guided by proven professionals.
Risk Mitigation
Address potential challenges from development to manufacturing from the get-go, ensuring consistent quality and regulatory compliance.
Our Capabilities
Your challenges handled from preclinical to commercial.
Engineers, Chemists, & Techs Dedicated To Pharma Tech Transfer.
Screen your Drug candidate is viable for further development and ensure the safety of clinical trial participants.
Formulation
Pre-formulation, dosage design, process development, and scale-up with analytical methods for pharmaceuticals.
Ensure global compliance, streamline approvals, & support product lifecycle with strategic regulatory planning & quality assurance.
Over 200+ analytical scientists to provide comprehensive analytical testing and method development for quality, validation, and compliance.
Our comprehensive services encompass Small, Pilot, Full-scale, and adaptive Manufacturing solutions across all phases of clinical trials
Raw Material Sourcing, Vendor Management, Inventory Management, Demand Forecasting, Cost Optimization.
supply chain coordination, adherence to international shipping regulations, logistics, and ensuring product integrity across diverse markets and climate.
Crafting compliant, stable global packaging with emphasis on material selection, tech & multilingual labeling for diverse patient needs.
Large pharmaceutical production that ensures quality, efficiency, compliance, advanced manufacturing, & streamlined processes for timely delivery.
Strategic planning & ongoing optimization for market impact, addressing trends, regulations, & tech advancements ensuring sustained relevance & profitability.