TPP Tech LLC.
U.S.-Based Manufacturing
TPP’s subsidiary, Contract Development and Manufacturing Organization— Societal CDMO San Diego. It specializes in the production of seven dosage forms, including Sterile Injectables, Sterile Ophthalmic Drops, Tablets, Capsules, Oral Liquids, Non-Sterile Liquid Syringes, and non-sterile Liquid Powder Syringes.
Comprehensive Capabilities
The Societal CDMO San Diego
Pharmaceutical Development Capabilities
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Societal San Diego CDMO is a US-based pharmaceutical contract development and manufacturing organization (CDMO) that can support your product from the early stages of chemistry, manufacturing, and controls (CMC) development to its first commercial launch and beyond. Our friendly and professional teams enable you to connect directly with project managers and actual pharmaceutical scientists working on your. We are dedicated to helping you navigate the intricate landscape of science, development, logistics, and regulations to ensure your pharmaceuticals are successfully approved and delivered to your patients.
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Formulation & Product Development
Our expertise spans a wide range of complex dosage forms, supported by full laboratory capabilities that often lead to intellectual property (IP) generation.
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Key services include:
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Physical Characterization & Excipient Compatibility
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Dosage Form Design & Solubility Assessment
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Process Design, Optimization, and Scale-Up
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Technology Transfer & Manufacturing Readiness
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Manufacturing Excellence
We provide end-to-end manufacturing solutions, from early-phase clinical batches to full-scale commercial production. Our structured technology transfer, quality control, and assurance teams ensure seamless oversight of drug manufacturing.
Key Capabilities include:
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Milling & Blending
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Compression & Encapsulation
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Spray & Rotary Granulation
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Particle & Bead Coating
Customer Journey
When you choose to collaborate with Societal San Diego CDMO, your project manager will connect you with our team of subject matter experts who will handle your project. The project manager will oversee and direct your project through all stages, from pre-IND activities to analytical and formulation development, delivery of cGMP clinical supplies, scale-up engineering, registration batches, pivotal stability, and PPQ and commercial supply. With a focus on transparency and open communication, our experienced team will ensure you receive the attention required for the sustained success of your project.