Clinical Supply Manufacturing Tailored to Your Needs
Overcome complexity and variability in manufacturing clinical trial materials for nucleic acid therapeutics by partnering with our highly experienced team in state-of-the-art facilities. Our flexible solutions prioritize preserving materials and bringing your compound to market faster while meeting all current quality, health, and safety standards. Leverage our extensive GMP clinical supplies manufacturing and packaging capabilities.
The configuration and management of our clinical manufacturing sites allows our team to respond to your unique needs and remain agile and response as your project scales or pivots. With our expertise, you can have peace of mind that your clinical supply manufacturing is in good hands, allowing you to focus on your core competencies in drug development.
When you partner with us, our packaging, kitting, and labeling services are particularly valuable to ensure product uniformity, scalability, and process validation. Our team is seasoned in solving complex challenges, and we are ready to support your project’s specific requirements.
Trust your aseptic fill-finish clinical supplies to our team with a history of successful media fills and cleanroom certification. Safety and sterility of products are of utmost importance here, with the filled material subject to release testing and examination from QC and QA groups before shipment to a clinical site. Our aseptic fill finish capabilities include many container closure types, including vials, syringes, and ampules. We adapt our manual or automated systems to your process specifications in a controlled environment designed to minimize contaminants, such as microorganisms and airborne particles.
Integrated Laboratory Services
When your team needs additional CDMO support, our scientists are ready. Our state-of-the-art facilities and highly trained experts can add power to your project.