Manufacturing

Tetra Pharm Technologies delivers reliable, compliant, and scalable biomaterials for pharmaceutical development. From GACP/GMP-certified starting materials to precision extraction, advanced synthesis, and seamless filling, we ensure quality, efficiency, and regulatory compliance at every stage. Our expertise in formulation, packaging, and traceability supports a secure, stable, and innovative pharmaceutical supply chain.

  • We have our own GACP/GMP biomaterials facility, ensuring consistent access to standardized, compliant, and safe starting materials. This minimizes potential supply chain disruptions while maintaining control over standards and volumes.

    We are also able to source starting materials through our partners or collaborate with you to use your production assets, helping enhance your core capabilities to bring new products to the market.

  • Precision pharmaceutical-grade GMP certified extraction and reliable results ensure the use of appropriate starting materials with a clear regulatory pathway to market while maintaining a stable supply chain to minimize risks from fluctuations in availability or price.

  • Tetra Pharm Technologies offers a range of specialized services to support pharmaceutical development. We accelerate development to create scalable and reliable solutions for therapies. Our expertise ensures purity, efficiency, and regulatory compliance while minimizing production risks at every stage.

    We provide well-characterized and documented substance and process development for naturally occurring compounds, including phyto, semi-synthetic, and synthetic variants.

    Additionally, we apply innovative formulation technologies to enhance bioavailability and improve stability. Our proprietary, IP-protected emulsion technology offers advanced solutions for pharmaceutical formulations.

  • Tetra Pharm Technologies offers seamless filling solutions, enabling faster time to market with a variety of Finished Dosing Forms (FDF). Our filing assets adhere to the highest quality pharmaceutical standards, minimizing risk while ensuring compliance and consistency.

    We provide multi-format capacities with precise dosage control and advanced container closure technology, ensuring seamless integration with all available finished dosing forms, with compliance verified on-site. Additionally, we offer automated electronic batch records to guarantee full traceability.

    While we have the capabilities to support your filing needs, we would also support you if you would like to use your own filing and finishing assets by supplying bulk and semi-finished formats to transfer key finishing steps to your own facilities.

  • At Tetra Pharm Technologies, we offer secure, compliant, and market-ready labelling and packaging. Our in-house labelling and packaging process ensures that your final product is fully prepared for direct shipment to you or a third-party distributor.

    We handle serialization for global markets, ensuring traceability and compliance. Additionally, our Quality Assurance team makes sure that all documentation is accurate and complete, while packaging adheres to local regulatory requirements.