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Description:We are a trusted end-to-end contract development and manufacturing organization (CDMO) partner for the pharmaceutical, biotech, and life sciences industries. Contact us to learn...
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Explore how our CDMO services can take your biologic further at BIO 2024. Schedule a meeting. Learn more Search Patheon × Recent searches Clear History Suggestions All Results Cancel Search Menu Back | Innovative solutions Integrated offerings Digital enablement Manufacturing Supply chain Our capabilities Small molecule API Oral solid dose Softgels Steriles Large molecule Biologics Steriles Advanced therapies Viral vectors Cell therapy mRNA Translational Services Clinical trial services Cold chain logistics and management Strategic comparator sourcing Clinical packaging services Clinical label services Commercial services Regulatory services Insights & resources Insights and resources Events Meet the experts Pharma insights blog Global site locations Get in touch Blog Contact us Thermo Fisher Scientific visit thermofisher.com visit thermofisher.com × Recent searches Clear History Suggestions All Results Search US | EN Contact us Innovative solutions Integrated offerings Customizable solutions backed by a science-driven, risk-based approach to reduce development timelines. Digital enablement Leverage the latest digital solutions and best practices for smarter drug development. Manufacturing Manufacturing solutions and continuous quality improvement that set the standard in the pharma industry. Supply chain Instilling confidence with proactive supply chain strategies for risk mitigation. Our capabilities Small molecule API Oral solid dose Softgels Steriles Large molecule Biologics Steriles Advanced therapies Viral vectors Cell therapy mRNA Translational Services Clinical trial services Cold chain logistics and management Strategic comparator sourcing Clinical packaging services Clinical label services Commercial services Regulatory services Insights & resources Insights and resources Stay connected to new discoveries, innovations, and expert scientific opinions. Events Check out upcoming industry events and schedule meetings. Meet the experts Have a question? Connect with one of our subject matter experts, read their work, and more. Pharma insights blog Catch up on the latest articles by our technical and scientific subject matter experts. Global site locations We provide CDMO services for drug development, clinical trial logistics, and commercial manufacturing to customers. Get in touch We want to hear from you. Contact a Thermo Fisher Scientific representative. Blog Home You deserve a CDMO partner you can trust Moving from molecule to medicine requires end-to-end solutions, global expertise, technical capabilities, and a strategic partner you can count on Play video Find your missing element 2024 CDMO leadership awards recipient In 2024, Thermo Fisher Scientific was awarded five leadership awards for our contract development and manufacturing organization (CDMO) services View press release View awards Transforming CDMO partnerships through quality Learn why bringing your innovative therapy to market requires working with a CDMO partner that embraces quality as a holistic endeavor Download whitepaper You’re invited: May 30 facility opening in Bleiswijk, Netherlands Please join us to celebrate the grand opening of our new state-of-the-art facility dedicated to delivering cold and ultracold supply chain solutions tailored for high-value therapies. Learn more End-to-end advanced therapy development and manufacturing services Over 20 years of cGMP manufacturing experience, expanding capacity, and global supply network View brochure Cell and gene therapies in the US vs. the EU: Top five areas of differentiation For cell and gene therapies (CGTs) and other complex biologics, US and EU regulatory processes vary by more than just jurisdictional oversight. In this eBook we share the five key differences in the drug development and review process for companies hoping to gain market access through US Food and Drug Administration (FDA) or European Medicines Agency (EMA) approval—as well as tips for navigating these differences. Cell and gene therapies in the US vs. the EUs Explore the major differences in the drug development and review process for companies in the US vs. the EU. View ebook Experience end-to-end cold chain supply solutions Ensure your temperature-sensitive materials are safe with our reliable, end-to-end cold chain logistics services and support. Explore more Discover a truly end-to-end supply chain solution Thermo Fisher Scientific is helping to revolutionize the world of cold chain logistics with our truly end-to-end supply chain solutions. From cold to cryo, we can handle a wide array of biomaterials, with services spanning transportation, warehousing, labeling, packaging, and distribution. Learn more about our industry-leading capabilities here . Critical biological material management Download our fact sheet to discover how we deliver life-changing treatments to patients in need. Download now Experience unparalleled expertise in spray drying Improve the solubility and bioavailability of your poorly water-soluble molecules with our spray dried dispersion services, from early development to commercial scale-up. Learn more Clinical trial services that can be tailored to your unique trial needs Our services span IMP, comparator, and ancillary clinical supplies, including strategy, sourcing, management, packaging and labeling, storage, and distribution View infographic Aseptic fill finish at the volumes you need, and at the quality you demand With flexible solutions to fit your unique timeline and budget View steriles brochure Tips for achieving technology transfer success Technology transfers can be tricky. A misstep or delay in one area can snowball into problems in other areas of the project. Likewise, inadequate planning or poor execution can introduce major risks and put the end goal of the project in jeopardy. The necessary foresight and a detailed project plan are essential elements to ensure the project runs smoothly, both on-time and on-budget, to achieve the ultimate end goal of regulatory approval. Check out our infographic to learn the 9 key tips for making your tech transfer easy and painless. Top tips for painless tech transfers Discover our top tips for a smooth and successful tech transfer. View infographic Delivering the elements of a strategic CDMO partnership Bringing medicine to patients requires science, technology, and world-class expertise. It also requires a strategic partnership—bonded by key elements such as trust, communication, and collaboration. At Thermo Fisher Scientific, we serve the pharmaceutical, biotech, and life sciences industries as a strategic contract development and manufacturing organization (CDMO) and clinical services partner. We believe that strategic partnerships fuel success, and we embed the elements of partnership into every operation, interaction, and step across your unique drug development journey. Through these elements, we can navigate everything from complex supply chain issues and compressed timelines to evolving regulations and a global pandemic. We know your challenges and have developed solutions you can trust to help bring your treatment to market faster. How we can partner with you We are your strategic partner for integrated drug development. We share your goals of improving patients’ lives and making the world a healthier place. Dedicated to excellence through effective partnership, we take pride in our collective ability to help you at every step of the development lifecycle, working as one team for a seamless experience. Explore our end-to-end solutions and capabilities, access our extensive resource library, and learn the benefits of having a partner with global expertise. Innovative solutions Get new medicines to patients faster. Our CDMO and clinical trial services simplify and accelerate your journey to market. Learn how Our capabilities Remove barriers in the drug development process- from early development through communication and everything in between. Explore our CDMO...
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