Millipore® CTDMO Services delivers expertise and flexible solutions for viral vector development and manufacturing to advance cell and gene therapies from preclinical through commercial production.
Our proficiency with adeno-associated virus (AAV), lentivirus, adenovirus, and other vectors helps streamline the development and manufacturing of cell and gene therapies. From early preclinical through clinical and commercial manufacturing, we offer the comprehensive experience, capabilities, and knowhow to advance cell and gene therapies to market.
Our viral vector experts are dedicated to supporting the advancement of cell and gene therapies throughout the product lifecycle. Discover how we apply our unparalleled experience, track record, and solutions to de-risk production from pre-IND to commercial supply.
Our viral vector experts work with our clients to identify and evaluate improvements to current processes in order to streamline therapeutic production, address risk, and accelerate cell and gene therapies to the clinic. Through our manufacturability assessments, we:
Our experienced Process Development teams incorporate a virus-specific and holistic approach to develop robust and optimized processes to support preclinical through commercial needs.
Our Analytical Development services are tailored to support the success of cell and gene therapies with individualized phase-appropriate testing and support.
Our flexible operations and capacity support clinical through commercial upstream and downstream GMP manufacturing for cell and gene therapies.
To streamline cell or gene therapies to market, we offer on-site clinical and commercial fill/finish services, as a continuation of GMP manufacturing.
Throughout the cell and gene therapy development and manufacturing lifecycle, we leverage the same expertise that has seen us through inspections by global regulatory agencies – 6 and counting – to provide dedicated and customized support for regulatory filings, inspections, and responses.
Our track record includes successful regulatory inspections by the U.S. Food & Drug Administration (FDA), the European Medicines Agency (EMA), Health Canada, the Pharmaceuticals and Medical Devices Agency (PMDA) of Japan, the Australian Therapeutic Goods Administration (TGA), and the Brazilian Health Regulatory Agency (ANVISA).
Our team of viral vector experts are accomplished in the development and manufacture of a diverse range of viral platforms, such as HSV, reovirus, echovirus, and more. We have supported more than 1,000 viral vector batches from process development to manufacturing with know how to support your viral vector therapeutics. Contact us to explore our capabilities and discuss your project needs.
We are dedicated to accelerating the development timelines for cell and gene therapies. Discover how we leverage our 30 years of experience, knowledge and expertise in viral vector development and manufacturing to provide a de-risked, reproducible and streamlined path to clinical and commercial manufacturing through our viral vector platforms.
With over 300 batches produced, we have extensive lentivirus development and manufacturing experience for cell and gene therapies.
We have significant experience in AAV development and manufacturing to quickly progress gene therapy programs from development to manufacturing.
Our teams have supported over 115 adenovirus clinical programs and have produced over 100 GMP batches. This deep expertise and understanding allows us to develop optimized approaches for adenoviral vector manufacturing.
Our team of viral vector experts are accomplished in the development and manufacture of a diverse range of viral platforms, such as HSV, reovirus, echovirus, and more. We have supported more than 1,000 viral vector batches from process development to manufacturing with know how to support your viral vector therapeutics. Contact us to explore our capabilities and discuss your project needs.
We are a single organization with a global network to deliver CDMO services across all stages of the molecule value chain. Our recently expanded viral vector CDMO campus in Carlsbad, California, USA increases production capacity and allows us to provide end-to-end solutions for viral cell and gene therapies in a single facility.
Offering end-to-end viral vector services, our 157,000 sq. ft. state-of-the-art facilities house upstream and downstream production suites, along with fill/finish, warehousing, QC labs, in addition to process and analytical labs to support early phase development to commercial manufacturing of suspension and adherent-based cell and gene therapy platforms.
Connect with us to explore first-hand our large-scale manufacturing facility and quality control labs to learn how our team delivers safe and reliable cell and gene therapy products.
In this webinar, our viral vector innovation team examines how they optimized and defined upstream and downstream processes to deliver a de-risked, reproducible, and accelerated path to GMP manufacturing, while providing high yield and quality lentivirus.
Hear from our viral vector experts as they showcase our capabilities and solutions for cell and gene therapy production and highlight key features of our technologies and GMP facility.
Join our viral vector process and analytical development (PAD) team for this on-demand webinar to discover our strategies for developing robust processes and analytics to ensure efficient and de-risked manufacturing.
Learn how our Manufacturability Assessment can help identify and address development and manufacturing challenges when bringing new therapies to market.
Discover how partnering experienced viral vector CTDMO can help guide you through the complexities of manufacturing and overcome regulatory hurdles to bring new therapies to patients.
In this white paper, learn why is important to establish an analytics program in early clinical development, and how partnering with an experienced CDMO that can establish an data-driven, streamlined analytics approach is key in accelerating program development.
Watch the video and read the poster to learn how we optimized our VirusExpress® platform for lentiviral vectors to maximize titers, enrich recovery, and reduce time to GMP manufacturing.
In this article, we explore how establishing an innovative DoE approach helped optimize the transfection and scale up of an AAV-based gene therapy.
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