CD Formulation offers comprehensive commercial manufacturing solutions for transdermal formulations, ensuring the highest quality standards and regulatory compliance. Leveraging our expertise in transdermal systems, advanced technologies, and a dedicated team, we provide seamless support to transition your product from pilot-scale production to full commercial success. Our high-quality, efficient, and flexible manufacturing services are tailored to meet the diverse needs of pharmaceutical companies, helping to accelerate product development and market entry.

Introduction to Commercial Manufacturing for Transdermal Formulations

Pharmaceutical commercial production refers to the development, clinical trials, and regulatory approval of new pharmaceutical products or pharmaceutical products on the market, to meet the market demand, the pharmaceutical products are carried out in a large-scale, standardized production process. The commercial production of pharmaceutical products is an important link for pharmaceutical enterprises to realize the market supply of new pharmaceutical products. They should follow production regulations for commercialization to ensure stable product quality and meet market demand. Monitor the production process in real-time and inspect it regularly to guarantee product quality.

Comprehensive Commercial Manufacturing Services We Offer

CD Formulation is a CDMO offering commercial manufacturing for various transdermal formulations. We handle gel, cream, ointment, spray transdermal formulation, and transdermal patch. We provide full technical guidance, not just in commercial production, but in every drug development detail. This support covers the entire production cycle, including:

• Synthesis process development and optimization
• Process verification and process transfer
• Analytical method development and validation
• Stability study
• Packaging and labeling services
• Preparation of toxicological batch and application batch of raw materials
• GMP preparation of clinical bulk drug
• Commercial manufacturing

What Can We Offer?

• Formulation Optimization: We improve drug formulations for better transdermal absorption, bioavailability, and stability.
• Process Improvement: We refine production processes to ensure uniform, high-quality transdermal products for commercial use.
• Strict Quality Standards: We enforce strict quality controls to meet regulatory requirements throughout production.
• Stability Studies: We assess product quality changes under different storage conditions to set expiry dates.
• Registration & Application Assistance: We help with transdermal product registration, including preparing materials and communicating with regulators.
• Compliance Production: We follow GMP and other relevant regulations to avoid compliance risks.

Innovative Technologies for Commercial Transdermal Production

Penetration promotion technology

• Chemical penetrant
• Mechanical microneedle
• Thermal/RF ablation and laser ablation

Nanotechnology and transdermal delivery

• Microemulsion
• Vesicle delivery system
• Nanoparticle
• Dendritic macromolecules

State-of-the-Art Manufacturing Facilities

• Vacuum homogenizing emulsifier (lower homogenizing) 30~160L
• Vacuum homogenizing emulsifier (upper homogenizing) 15~25L
• High-speed shear dispersing machine 0.25-30L
• Automatic filling and sealing machine (aluminum pipe, composite pipe) 2000~4000 pieces/hour
• Vacuum homogenizing emulsifier 500~1000L

Why Choose CD Formulation?

• The rapid completion of the development of starting materials and APIs has obvious advantages in the control of material costs.
• Provide toxicological batch samples quickly, evaluate and test the toxicological batch samples to ensure the rationality of doping standards.
• Rapid identification, preparation, control, and establishment of reasonable quality standards for impurities involved in the project.
• Authoritative prediction of genotoxic impurities, formulation of limits, development of analytical methods, and scientific control strategies.
• Familiar with multinational regulatory and policy environment.

With extensive experience in transdermal formulation research and commercial-scale production, CD Formulation is committed to supporting pharmaceutical companies and researchers throughout the entire production cycle. From process scaling to regulatory adherence, we offer end-to-end services that ensure stable and reliable product quality. Partner with us to turn your innovative formulations into market-ready products. For personalized assistance, contact us, and our team will respond within three business days.