Good Morning from Salt Lake City! We’re kicking off day 1 of PharmSci360! Stop by booth #1713 and chat with us on our BioA and GMP analytical capabilities.
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Dr Kayla Preece, ND, DABT, Staff Scientist/Toxicologist at GRAS Associates, has written a captivating article about considerations in ingredient safety, and it’s officially live on our website. Read here: https://lnkd.in/g_uY7Ndd - #IngredientSafety #IngredientTesting #ToxicologicalTest #NovelIngredient #RegulatoryStrategy #Regulatory
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Brushing up on our GMP knowledge! 💡 Earlier this year, the GMP experts from ImproveMatic held a course at H&V. With new colleagues joining us over the summer, we figured it was the perfect time to refresh our GMP knowledge to stay on top of industry trends. In the session, we talked about GxP and why it’s so important. With our varied GMP backgrounds and experience levels, we had some great discussions, shared real-life industry stories, and talked about industry trends and key focus areas from regulatory authorities. Big thanks to ImproveMatic and Naram El-Shamary!
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DistillerSR will be at RAPS Convergence 2024! Visit us at booth #419 for a live demo and to learn more about how we can help you streamline your regulatory submissions and time to market. Book a meeting with our team: https://bit.ly/4cXAhBg #DistillerSR #systematicliteraturereviews #evidencemanagement #medicaldevices #IVDs #regulatoryaffairs #RAPSConvergence
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Today is the day! Veristat’s Regulatory Team is pleased to welcome you to the TOPRA Symposium, the ideal forum for discussing the latest developments in regulatory affairs. Join us at Booth #23 to discuss how we can help you tackle your next product development or commercialization challenge. #TOPRAsymposium #Regulatory TOPRA - The Organisation for Professionals in Regulatory Affairs Delphine Guérin Martin Kretz John Kirk Anja Bührer
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Part 2 of Beyond Compliance: Exploring Controls in Microbiological Air and Surface Testing by Christine Hong is the feature article in the November 2024 issue of SCQM by Pharmacy Stars. An excellent article, we might add. ✍ After reading, share your comments. #pharmacystars #SCQM #sterilecompounding #compoundingquality #USP797 #USP800 #pharmacytechnician #pharmacist #environmentalmonitoring
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Join us for a discussion about one of the "infamous" viruses in the biomanufacturing. #adventitiousagentscreening #nextgenerationsequencing
Join us for an insightful webinar on Adventitious Agent Testing for MMV. This session will dive deep into the challenges and advancements in testing for adventitious agents in biological products. Whether you’re a professional or new to the field, this is a must-attend event to stay ahead of the curve in biopharma safety and quality assurance. Don't miss out on this opportunity to expand your knowledge and connect with experts in the field! 🔗 Register here: https://lnkd.in/dfShvBwh
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How to avoid ineffective approaches to Cleaning Validation? https://lnkd.in/dmbCHgut 📣 Three weeks untill Cleaning Validation Online Summit! Participate in our webinar sessions to develop a practical and compliant Cleaning Validation program and make sure that contamination won't compromise the quality of your upcoming product. The latest agenda to check for speakers, sessions and more https://lnkd.in/g9SQfmJ2
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Looking forward to our webinar tomorrow where we will discuss challenges in the vaporizer space and how we are addressing them to move this industry forward!
Join Audra Horridge alongside Shawna Vreeke, PhD of True Terpenes, and Darwin Millard of CSQ Cannabis Safety & Quality on Wed, July 31st at 11am PST to talk about common issues and what we are doing to move the industry forward in a safer and informed way. Tap the link in our profile to reserve your spot⚡️. Panel led by Bethany Moore and David Vaillencourt The GMP Collective. Register below: https://lnkd.in/gDhv4wmp
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Quality team for a webinar on quality to mark World Quality Day! A big thank you to our speakers, Ciriaco Maraschiello (He/Him) and Beatrice Bellanti, for sharing insights on: 📌 The role of quality in the discovery process 📌 How ISO 9001 enhances early drug discovery 📌 Safeguarding data integrity with ISO 27001 Stay tuned for more highlights! If you missed us today, the webinar will be available on our website next week. #WorldQualityDay #ISOcertification #DrugDiscovery #Webinar
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GMP equalisation – a potential hurdle in the PRT fast lane? GMPe, by its very nature, involves intricate calculations, multiple stages and data interrogation and analysis. For schemes eager to secure full buyouts and individual policies today, a lengthy delay in completing GMPe is far from ideal. There are solutions entering the market that can help though. Solutions that can dramatically reduce the time required to complete GMPe work at scale. Read the full article here: https://lnkd.in/e8cCq8EM
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Bringing the best kept secret in supporting your product's development from discovery through GMP release with 30+ years experience. Senior Director Business Development at Prolytix.
2moExcited for the week in Utah