At Scilife, we help people and companies transform quality into a catalyst for value creation, making Smart Quality a culture and infusing it throughout the entire organization. This recasts quality as a competitive advantage instead of a simple regulatory requirement.
But, what embeds quality into a company’s culture? And how, exactly does an organization benefit as a result? These questions are at the core of Scilife.
The Scilife Smart Quality Platform brings clarity to quality and compliance by combining powerful quality management tools with advanced data analytics, augmented learning, and gamification.
Hundreds of leading life sciences companies worldwide like Novartis, Biocartis, Yusen Logistics, Polpharma, Pendulum, and many more trust Scilife to manage their quality processes, empower employees to take quality ownership, enhance efficiency, and reduce compliance risk. The impact? Improving patients’ lives.
Ready for the bright future of Smart Quality? ➡️ scilife.io
Thank you so much for your question, @eslamelsamahy7528! In the context of ISO 19011:2018, monitoring and reviewing are distinct but complementary activities that ensure the effectiveness and continuous improvement of an audit programme. - Monitoring involves the ongoing evaluation of the audit programme to ensure that its objectives are being achieved. It includes ongoing evaluation, continuous assessment, and feedback mechanisms. - Reviewing is a more comprehensive process that involves a systematic examination of the audit programme to identify needs for changes and opportunities for improvement. I hope this clarifies the difference for you. We're here to assist you with any further questions or clarification you may need! :)
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Hi, @aminebahlou9158! Thank you for your positive feedback and inquiry about ISO 19011 training support. While we don't currently offer specific training on ISO 19011, your interest is greatly appreciated, and we'll definitely keep it in mind for future content. In the meantime, feel free to explore our playlist covering risk-based auditing according to ISO 19011:2018 - ru-vid.com/group/PLXDFJne8VYYqV7u3WibBRHsXnaSB2OcUY&si=hP2BQtyiB3dRx67A We hope you find it beneficial! If you enjoy our content, don't forget to subscribe for more updates, and if you find the video helpful, please give it a thumbs up :)
Thanks for your comment, @ayshariaz1693! Absolutely, we'll be covering the rest of the ISO 19011 clauses in our upcoming videos. We drop a new video on our channel every week, so keep an eye out!
Thank you for acknowledging the explanation of 21 CFR Part 11! Regarding CSV trainings, we highly recommend considering "Quality Systems, Computer System Validation (CSV), and Data Integrity": www.scilife.io/events-and-webinars/qa-csv-data-integritry-with-yves-dene. Thank you for bringing the broken link to our attention. We sincerely apologize for the inconvenience this may have caused. We have now updated the link, and you can access the correct one here: QA CSV Data Integrity with Yves Dene. We appreciate your understanding and support.. This AMA Webinar, with Yves Dène, offers comprehensive insights into CSV practices, aligning with regulatory standards and emphasizing data integrity within the GAMP framework. Additionally, we attach two extra resources available on our website that complement your learning: - CSV vs. CSA: What are the main differences? www.scilife.io/blog/csv-csa-main-differences - GAMP 5 and GAMP 5 2nd Edition: What are the main differences? www.scilife.io/blog/gamp-5-and-gamp-5-2nd-edition-differences
@@Grace-jb7me Thank you for pointing out the issue with the link. We apologize for any inconvenience this may have caused. You can now access the correct link in the comment, or you can use this direct link: www.scilife.io/events-and-webinars/qa-csv-data-integritry-with-yves-dene. We appreciate your understanding and support!
