Ever wondered about the intricate web of logistics behind #cellandgenetherapy #clinicaltrials? From sourcing specialized equipment to navigating regulatory requirements, every step is crucial in bringing innovative treatments to patients in need. We understand the nuances of these complex supply chains and have developed an end-to-end process to support your cell and gene therapy trial every step of the way. » https://bit.ly/3V8YOOd
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Have you read our recently released target product profile (TPP) guide and want to learn more about how to develop an effective TPP for successful therapy adoption? Join our webinar on the 31st of January titled 'Developing a robust target product profile (TPP) for successful therapy adoption', where Cell and Gene Therapy Catapult’s experts in #MarketAccess, #RegulatoryAffairs and #NonClinical strategy will talk through the guide, discuss the value of a TPP and how to approach building one. Register now: https://buff.ly/3RqT2nC #TargetProductProfile #CellTherapies #GeneTherapies #TherapyDevelopers
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EMPOWERING CDMOS: THE VIRTUOSI ADVANTAGE Top 5 reasons global CDMOs choose Virtuosi® for their educational needs: 1. Gain a Competitive Edge: Accelerate talent onboarding and competency building, giving your team a strategic advantage. 2. Unmatched Knowledge Retention: Achieve an impressive 80% knowledge retention even after a year, ensuring lasting impact. 3. Time is Money: Experience reduced training times, allowing you to maintain focus on your core operations. 4. Slash Operational Costs: Save on SME time and minimize aseptic area incursions, leading to significant cost reductions. 5. Consistent Quality Across Sites: Standardize quality results seamlessly across and within sites, ensuring excellence every step of the way. Maximize your CDMO excellence with Virtuosi – Elevate your team's expertise today: https://lnkd.in/eHVJirvT PARTNER SPOTLIGHT: Charles River Laboratories Check out the video below to see Virtuosi in action at Charles River Laboratories' cutting edge training facility. Our shared belief in the pivotal role of education is evident in their forward-thinking approach to staff training. Imagine the possibilities for YOUR company – revolutionize your training experience and elevate your team's expertise. #pharma #biotech #qualityassurance #training #cdmo
Our Memphis Facility has everything you need to take your cell and gene therapy from concept to cure, including integrated QC testing, 25+ state-of-the-art processing suites, highly trained experts, and an unmatched regulatory track record. Want to see for yourself? Take a virtual tour: https://okt.to/0J9WOU
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Managing Director: Impact Shine Communications. Experienced Public Relations, Marketing Communications, Government Relations & IR Expert. Consultant Director: Influence Associates. WBF: Advisory Board Member.
Ultra-rapid Detection of Live Microbes
Will you join us tomorrow? Register for our live webinar: Rapid Sterility Testing for Cell and Gene Therapy Products. We will be online on June 18th at 14.00 CEST. Anyone who registers will also get access to the replay. After registering, you will receive a confirmation email about joining the webinar. https://lnkd.in/dkHEsQGr #RapidSterilityTesting #CellGeneTherapy #CGT #CRISPR #CART
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There are many obstacles with managing the ancillary materials used in the production of cell and gene therapy products. In this webinar, sponsored by BioLegend, we discover the critical qualities of cytokines, growth factors, antibodies and culture media and risk-based strategies for assessing these challenges. Register now >>> https://hubs.ly/Q02HD5hk0
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ICYMI: Listen to Dr. Salvador Rico, CMO of Encoded Therapeutics Inc., discuss the company's gene therapy and overall program looking to tackle #DravetSyndrome https://lnkd.in/eZkjigEh #InternationalEpilepsyDay Dravet Syndrome Foundation
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Sr. Product Specialist at ThermoFisher Scientific - BioProduction Group - Pharma Analytics Division
Want to know the latest regulations on residual DNA and the quantitation of host cell and pDNA? We’ve captured the details of a discussion on regulatory guidance with an industry thought leader. Read on to discover critical steps for the testing and characterization involved in cell and gene therapy manufacturing: https://lnkd.in/gZ4djNp9 #bioprocessing #bioproduction #qualitycontrol #regulatorycontrol #hek293 #aav #genetherapy #celltherapy
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Emmes provides full-service clinical trial support for Cell and Gene Therapy, guiding you through each phase of development. With over 40 years of experience, we offer tailored solutions that help you navigate the complexities of clinical research, from regulatory support to data management. Read our fact sheet to see how Emmes can help you advance the future of medicine together. #CRO #ClinicalDevelopment #CellAndGeneTherapy #ClinicalTrials #Emmes
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📢 𝗜𝗧'𝗦 𝗔𝗟𝗠𝗢𝗦𝗧 𝗛𝗘𝗥𝗘! In just a few more days, we have some very exciting news to share. Stay tuned to our countdown to find out what this mysterious column solution is: https://bit.ly/3SOFwfb Can’t wait? The answer is within this poster presented at the 5th Annual Gene Therapy Analytical Development 2023 Conference in November.
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Want to know the latest regulations on residual DNA and the quantitation of host cell and pDNA? We’ve captured the details of a discussion on regulatory guidance with an industry thought leader. Read on to discover critical steps for the testing and characterization involved in cell and gene therapy manufacturing: https://lnkd.in/gZ4djNp9 #bioprocessing #bioproduction #qualitycontrol #regulatorycontrol #hek293 #aav #genetherapy #celltherapy
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