来源: Pharmaceutical Technology
来源: Pharmaceutical Technology
“This collaboration will enable us to utilise our cutting-edge GMP plasmid manufacturing platform technology to support the development of mRNA-based Covid-19 vaccine and its therapeutic candidates.” The company provides end-to-end contract development and manufacturing organisation (CDMO) services from the discovery to the commercialisation of drugs.
It continues to offer GMP materials, including plasmid DNA and the ancillary materials development for supporting the mRNA manufacturing process, as RVAC advances its mRNA candidates’ development. The GenScript ProBio team also offers consultative and expert guidance concerning the regulatory and quality expectations of agencies globally. To support the mRNA initiatives, RVAC Medicines will continue to partner with GenScript ProBio for the clinical-stage development and commercial stage of its candidates. RVAC Medicines CEO Dr Sean Fu said: “We are excited to work closely with GenScript ProBio. With its technical strength and customer-centric approach, GenScript ProBio will help to accelerate the development of RVAC’s pipeline.” In July last year, GenScript ProBio and ACT Therapeutics entered a strategic collaboration memorandum of understanding (MoU) to develop a next-generation chimeric antigen receptor (CAR)-T cell therapy platform. Cell & Gene Therapy coverage on Pharmaceutical Technology is supported by Cytiva.
Editorial content is independently produced and follows the highest standards of journalistic integrity. Topic sponsors are not involved in the creation of editorial content.
Optimise your cell therapy process: a guide to cell thawing
Typically carried out at the point of care, errors in cell therapy thawing could compromise treatment efficacy, leading to significant patient impact as well as high costs and a compromised reputation for the product’s developer.
This guide addresses how cell thawing has historically developed into the new techniques used today, along with the physical and biological implications of key metrics and components such as warming rate and ice structure. Also included are reviews of key studies from scientific literature and a consideration of the interactions between cooling and warming rates, as applicable to cell and gene therapies.
来源: Pharmaceutical Technology
By clicking the Download Free Whitepaper button, you accept the terms and conditions and acknowledge that your data will be used as described in the Cytiva Thematic privacy policy
By downloading this Whitepaper, you acknowledge that we may share your information with our white paper partners/sponsors who may contact you directly with information on their products and services.
Visit our privacy policy for more information about our services, how we may use, process and share your personal data, including information on your rights in respect of your personal data and how you can unsubscribe from future marketing communications. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address.