Business Details
50+ Years
experience
Trusted Pharmaceutical CDMO for Semi-Solid & Liquid Dosage Forms
For over 80 years, DPT Laboratories has been a trusted leader in pharmaceutical development and manufacturing, specializing in semi-solid and liquid dosage forms. Our expertise spans the entire product lifecycle, from pre-formulation research to commercial-scale production, ensuring seamless transitions for clients. We maintain rigorous quality control aligned with current Good Manufacturing Practices (cGMP) to deliver reliable, compliant solutions. Our team of scientists and technicians brings decades of experience in therapeutic areas such as dermatology, pain management, and respiratory diseases. By integrating advanced technologies with personalized support, we help clients navigate complex development challenges and scale-up processes.Our commitment to innovation and quality is reflected in every product we produce, serving as proof of our enduring legacy. We prioritize transparency, collaboration, and accountability, ensuring clients meet their delivery and regulatory goals. With facilities designed for precision and efficiency, we offer services including analytical testing, stability studies, and clinical trial supply management. Our focus on continuous improvement drives investments in process optimization and technical capabilities. For pharmaceutical companies seeking a dependable partner with deep industry knowledge, DPT provides the expertise and infrastructure to transform concepts into market-ready products.
Services
Pre-Formulation
Formulation Development
Analytical Testing
Clinical Trial Supplies
Packaging
Process Development
Stability Testing
Microbiology
Semi-Solid Manufacturing
Aerosol Production
Details
- Year established: 1938
Highlights and features
- We have over 80 years of experience in semi-solid and liquid pharmaceutical development.
- Our integrated services streamline the path from lab to market.
- We adhere to current Good Manufacturing Practices (cGMP) for regulatory compliance.
- Our team specializes in 12 therapeutic areas, including dermatology and pain management.
- We provide end-to-end support, including stability testing and clinical trial supplies.
Services
Pre-Formulation
Our pre-formulation services analyze drug properties to optimize development pathways. Scientists evaluate stability, solubility, and compatibility, ensuring efficient formulation design. This phase reduces risks and accelerates timelines for new chemical entities.
Formulation Development
We create customized formulations for semi-solids, liquids, and aerosols. Expertise spans creams, gels, ointments, and sprays across 12 therapeutic areas. Advanced techniques ensure bioavailability and patient compliance.
Analytical Testing
Comprehensive testing includes potency, purity, and stability assessments. Our labs use state-of-the-art equipment to meet regulatory requirements, ensuring product safety and efficacy throughout the lifecycle.
Clinical Trial Supplies
We manufacture and package clinical trial materials under strict cGMP conditions. Services include labeling, blinding, and distribution, supporting phases I-IV with precise documentation and traceability.
Semi-Solid Manufacturing
Large-scale production of semi-solid dosage forms using validated processes. Capabilities include emulsions, lotions, and ointments, with focus on consistency, scalability, and regulatory compliance.
Questions
What pharmaceutical services does DPT offer?
We provide end-to-end services including pre-formulation, formulation development, analytical testing, clinical trial supplies, and commercial manufacturing for semi-solids and liquids.
How long has DPT specialized in semi-solid dosage forms?
DPT has over 80 years of experience in semi-solid and liquid pharmaceutical development and manufacturing since 1938.
What therapeutic areas does DPT support?
We work across 12 therapeutic areas, including dermatology, pain management, respiratory diseases, pediatrics, and women's health.
Is DPT compliant with regulatory standards?
Yes, all manufacturing follows current Good Manufacturing Practices (cGMP) to meet FDA and international regulatory requirements.
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