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  <title>This Week in Compliance - November 2024</title>
  <description>Stay Ahead of the Curve: ISO 9001 Revision Insights</description>
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  <pubDate>Fri, 22 Nov 2024 14:51:43 +0000</pubDate>
  <atom:published>2024-11-22T14:51:43Z</atom:published>
    <dc:creator>Don Weobong</dc:creator>
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    <div class='beehiiv'><style>
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</style><div class='beehiiv__body'><ul><li><p class="paragraph" style="text-align:left;"><b>ISO 9001 is evolving to meet modern challenges!</b> The upcoming 2025 revision introduces deeper risk integration, digital transformation, sustainability, and enhanced customer focus. Expect updates in supply chain management, climate change considerations, and streamlined integration with other ISO standards. Also, don’t forget to sign up for the <a class="link" href="https://us02web.zoom.us/webinar/register/WN_blxbAtrwSEafaWM1E5pI_Q?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-november-2024" target="_blank" rel="noopener noreferrer nofollow">Quality Culture webinar</a>.</p></li></ul><hr class="content_break"><h3 class="heading" style="text-align:left;" id="webinar-developing-a-culture-of-qua">Webinar: Developing a Culture of Quality</h3><p class="paragraph" style="text-align:left;"><b>Title</b>: Developing a Quality Culture that Drives Compliance & Business Success.</p><ul><li><p class="paragraph" style="text-align:left;">This <a class="link" href="https://us02web.zoom.us/webinar/register/WN_blxbAtrwSEafaWM1E5pI_Q?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-november-2024" target="_blank" rel="noopener noreferrer nofollow">engaging session</a> is designed to help you foster a culture of quality within your organization and connect quality outcomes with business success.</p></li><li><p class="paragraph" style="text-align:left;">Join us for an informative presentation and an interactive Q&A session with industry experts. Learn best practices for engaging employees in continuous improvement and applying these learnings in real-world scenarios.</p><p class="paragraph" style="text-align:left;">Webinar Details:</p><ul><li><p class="paragraph" style="text-align:left;">Date: <b>December 17th, 2024</b></p></li><li><p class="paragraph" style="text-align:left;">Time: <b>1:00 pm, Eastern Time EST</b></p></li><li><p class="paragraph" style="text-align:left;">Duration: 40 minutes</p></li></ul><p class="paragraph" style="text-align:left;"><span style="text-decoration:underline;"><b><a class="link" href="https://us02web.zoom.us/webinar/register/WN_blxbAtrwSEafaWM1E5pI_Q?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-november-2024#/registration" target="_blank" rel="noopener noreferrer nofollow" style="color: rgb(0, 123, 255)">Register Here</a></b></span></p><p class="paragraph" style="text-align:left;"></p></li><li><p class="paragraph" style="text-align:left;">Secure your spot today and take the first step towards cultivating a quality-driven culture in your organization. The dynamic Cassandra Harbour will be presenting this session. We look forward to seeing you at the <a class="link" href="https://us02web.zoom.us/webinar/register/WN_blxbAtrwSEafaWM1E5pI_Q?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-november-2024" target="_blank" rel="noopener noreferrer nofollow">webinar.</a></p></li></ul><p class="paragraph" style="text-align:left;"><b>Featured Article</b>:</p><h3 class="heading" style="text-align:left;" id="the-globally-trusted-iso-9001-stand">The globally trusted ISO 9001 standard for Quality Management Systems is undergoing a significant revision, set to release in 2025. This update addresses the evolving challenges and opportunities faced by organizations in today’s dynamic landscape. Here&#39;s a sneak peek at what to expect:</h3><ul><li><p class="paragraph" style="text-align:left;"><b>Deeper Risk Integration</b>: Strengthened risk-based thinking to identify and mitigate risks while fostering resilience proactively.</p></li><li><p class="paragraph" style="text-align:left;"><b>Digital Transformation</b>: Emphasis on leveraging digital tools for quality management and ensuring data security.</p></li><li><p class="paragraph" style="text-align:left;"><b>Sustainability Focus</b>: Aligning QMS practices with global sustainability goals and environmentally responsible practices.</p></li><li><p class="paragraph" style="text-align:left;"><b>Enhanced Customer Centricity</b>: New strategies to gather and act on customer feedback for continual improvement.</p></li><li><p class="paragraph" style="text-align:left;"><b>Supply Chain Management</b>: Addressing supply chain resilience and supplier quality assurance.</p></li><li><p class="paragraph" style="text-align:left;"><b>Climate Change Considerations</b>: Preparing organizations for climate-related challenges and integrating these into QMS strategies.</p></li><li><p class="paragraph" style="text-align:left;"><b>Streamlined Integration</b>: A high-level structure for easier alignment with other ISO standards.</p></li></ul><p class="paragraph" style="text-align:left;">These updates ensure <a class="link" href="https://quality.eleapsoftware.com/advancing-beyond-the-basics-navigating-the-importance-and-complexity-of-quality-management-systems-qms/?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-november-2024" target="_blank" rel="noopener noreferrer nofollow">ISO 9001</a> remains a robust framework for quality excellence, adaptability, and global competitiveness.</p><h3 class="heading" style="text-align:left;" id="e-brief">eBrief:</h3><p class="paragraph" style="text-align:left;"><b>Title</b>: Comprehensive Guide to ISO 14971: Risk Management for Medical Devices</p><iframe allow="accelerometer; autoplay; clipboard-write; encrypted-media; gyroscope; picture-in-picture" allowfullscreen="true" class="youtube_embed" frameborder="0" height="100%" src="https://youtube.com/embed/oOEhJig2Tww" width="100%"></iframe><ul><li><p class="paragraph" style="text-align:left;"><b>Summary</b>: ISO 14971 is the global standard for risk management in the medical device industry. <a class="link" href="https://www.eleapsoftware.com?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-november-2024" target="_blank" rel="noopener noreferrer nofollow">eLeaP</a> provides an in-depth guide to understanding and implementing the risk management process, from identifying hazards to post-market monitoring. </p></li><li><p class="paragraph" style="text-align:left;"><b>View Video</b>: <a class="link" href="https://youtu.be/oOEhJig2Tww?si=YaWmQAc5Ebx-YNQA&utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-november-2024" target="_blank" rel="noopener noreferrer nofollow">https://youtu.be/oOEhJig2Tww?si=YaWmQAc5Ebx-YNQA</a></p></li></ul><h3 class="heading" style="text-align:left;" id="6-case-study">Resources:</h3><p class="paragraph" style="text-align:left;"><b>Title</b>: Access and download resources from our site</p><ul><li><p class="paragraph" style="text-align:left;"><a class="link" href="https://knowledgeessentials.eleapcourses.com/v7/computer-system-validation-fda-warning-letters-case-studies-lessons-learned-174386.html?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-november-2024" target="_blank" rel="noopener noreferrer nofollow">Computer System Validation – FDA Warning Letters Case Studies – Lessons Learned</a></p></li><li><p class="paragraph" style="text-align:left;"><a class="link" href="https://knowledgeessentials.eleapcourses.com/v7/the-gamp-approach-to-21-cfr-part-11-compliance-148301.html?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-november-2024" target="_blank" rel="noopener noreferrer nofollow">The GAMP Approach to 21 CFR Part 11 Compliance</a></p></li><li><p class="paragraph" style="text-align:left;"><a class="link" href="https://quality.eleapsoftware.com/resources/?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-november-2024" target="_blank" rel="noopener noreferrer nofollow">SOP Templates</a></p></li></ul><h3 class="heading" style="text-align:left;" id="about-us">About us:</h3><p class="paragraph" style="text-align:left;"><span style="color:rgb(13, 13, 13);font-family:Roboto, Noto, sans-serif;font-size:15px;">eLeaP is a trusted platform specializing in learning, compliance, and performance management for highly regulated industries such as life sciences, aviation, manufacturing, finance, and technology. Our platforms help organizations meet rigorous regulatory requirements like 21 CFR and 14 CFR, develop high-performing teams, and achieve exceptional results. Learn more at </span><span style="color:rgb(13, 13, 13);font-family:Roboto, Noto, sans-serif;font-size:15px;"><a class="link" href="https://www.eleapsoftware.com?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-november-2024" target="_blank" rel="noopener noreferrer nofollow">www.eleapsoftware.com</a></span></p></div><div class='beehiiv__footer'><br class='beehiiv__footer__break'><hr class='beehiiv__footer__line'><a target="_blank" class="beehiiv__footer_link" style="text-align: center;" href="https://www.beehiiv.com/?utm_campaign=4f35ee33-aaa6-4365-a334-132aa569ac5e&utm_medium=post_rss&utm_source=eleap_compliance">Powered by beehiiv</a></div></div>
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  <title>This Week in Compliance - August 2024</title>
  <description>Breakthrough in Gene Therapy – Latest Industry Insights!</description>
  <link>https://eleapcompliance.com/p/week-compliance-august-2024</link>
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  <pubDate>Fri, 16 Aug 2024 12:09:00 +0000</pubDate>
  <atom:published>2024-08-16T12:09:00Z</atom:published>
    <dc:creator>Don Weobong</dc:creator>
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</style><div class='beehiiv__body'><p class="paragraph" style="text-align:left;"><b>Welcome Message</b>:</p><ul><li><p class="paragraph" style="text-align:left;"><b>Introduction</b>: Welcome to the latest edition of This Week in Compliance (TWIC), your go-to source for the latest developments in quality and compliance. This month, we delve into groundbreaking research, expert opinions, and critical regulatory updates.</p></li></ul><hr class="content_break"><p class="paragraph" style="text-align:left;"><b>Featured Articles</b>:</p><h3 class="heading" style="text-align:left;" id="1-industry-news">1. Industry News</h3><p class="paragraph" style="text-align:left;"><b>Title</b>: Gene Therapy Breakthrough: A New Era in Medicine</p><ul><li><p class="paragraph" style="text-align:left;"><b>Summary</b>: Discover how the latest advancements in gene therapy are set to revolutionize treatment options. Recently, the FDA approved a novel gene therapy for the treatment of hemophilia B, offering a potential cure rather than lifelong management of the condition.</p></li><li><p class="paragraph" style="text-align:left;"><b>Read More</b>: <a class="link" href="https://www.pfizer.com/news/press-release/press-release-detail/us-fda-approves-pfizers-beqveztm-fidanacogene-elaparvovec?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-august-2024" target="_blank" rel="noopener noreferrer nofollow">here</a> and <a class="link" href="https://www.fda.gov/vaccines-blood-biologics/cellular-gene-therapy-products/beqvez?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-august-2024" target="_blank" rel="noopener noreferrer nofollow">here</a>.</p></li></ul><h3 class="heading" style="text-align:left;" id="2-research-highlights">2. Research Highlights</h3><p class="paragraph" style="text-align:left;"><b>Title</b>: Multi-Omics: The Future of Personalized Medicine</p><ul><li><p class="paragraph" style="text-align:left;"><b>Summary</b>: An in-depth look at how <a class="link" href="https://youtu.be/ieornWvarPE?si=h5-LmC3_9GWPz27P&utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-august-2024" target="_blank" rel="noopener noreferrer nofollow">multi-omics</a> is transforming biomedical research and clinical applications. Multi-omics approaches integrate genomics, proteomics, metabolomics, and more to provide a comprehensive view of biological processes and disease mechanisms. </p></li><li><p class="paragraph" style="text-align:left;"><b>AI in Multi Omics</b>: ​​Read about the leading innovators in AI-assisted multiomics within the pharmaceutical industry. AI in multiomics involves using AI and machine learning to integrate and analyze data from various omics sources, enhancing understanding of biological systems and improving diagnosis, treatment, and drug discovery. Key players include Illumina, BostonGene, and NantWorks, among others. The report highlights the innovation intensity and geographic reach of these companies&#39; patents, emphasizing the transformative impact of AI on pharmaceutical research and development.</p></li><li><p class="paragraph" style="text-align:left;"><b>Read More</b>: <a class="link" href="https://www.genome.gov/research-funding/Funded-Programs-Projects/Multi-Omics-for-Health-and-Disease?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-august-2024" target="_blank" rel="noopener noreferrer nofollow">here</a> and <a class="link" href="https://www.pharmaceutical-technology.com/data-insights/innovators-ai-ai-in-multiomics-pharmaceutical/?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-august-2024" target="_blank" rel="noopener noreferrer nofollow">here</a>.</p></li></ul><h3 class="heading" style="text-align:left;" id="3-expert-interview">3. Expert Interview</h3><p class="paragraph" style="text-align:left;"><b>Title</b>: Interview with Cassandra Harbour, Quality Management QMS Expert | RAQA Manager | ISO 13485 | ISO 900</p><ul><li><p class="paragraph" style="text-align:left;"><b>Summary</b>: Ms. Harbour shares her insights on various quality and compliance topics.</p></li><li><p class="paragraph" style="text-align:left;"><a class="link" href="https://quality.eleapsoftware.com/expert-interview-with-cassandra-harbour/?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-august-2024" target="_blank" rel="noopener noreferrer nofollow">Read More</a></p></li></ul><h3 class="heading" style="text-align:left;" id="4-e-brief"><b>4. </b>eBrief</h3><p class="paragraph" style="text-align:left;"><b>Title</b>: <span style="color:rgb(13, 13, 13);">Understanding the FDA Pre-Market Approval (PMA) Process for Medical Devices</span></p><div class="image"><a class="image__link" href="https://youtu.be/huAsGIx4YpU?si=NzoYe8EP3nsPL3JZ&utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-august-2024" rel="noopener" target="_blank"><img alt="" class="image__image" style="" src="https://lh7-rt.googleusercontent.com/docsz/AD_4nXddsZx3r3mtOPBZFN7oH-AONhkbt6HEOvZnf4Iok5rT9b_fkeBkiQ1C1JUAf5Arv-zP450hOrUaC1uiBWGaVUXh2cTb0w0G2WbvmrHLeV_LCTB5SiwqD9JT2Zn0FA-Vj3v3iPu_yKOHYLpnDP5hMfyp1jA?key=un7nTIequyKGaiMdKjt4EA"/></a></div><ul><li><p class="paragraph" style="text-align:left;"><b>Summary</b>: <span style="color:rgb(13, 13, 13);">Introduction to PMA: Understanding the stringent regulatory pathway for Class III medical devices. Importance of PMA: Why ensuring the safety and effectiveness of high-risk medical devices is crucial before they reach the market.</span></p></li><li><p class="paragraph" style="text-align:left;"><b>View Video</b>: <a class="link" href="https://youtu.be/huAsGIx4YpU?si=piMOnwn6CL-8dRQE&utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-august-2024" target="_blank" rel="noopener noreferrer nofollow">https://youtu.be/huAsGIx4YpU?si=piMOnwn6CL-8dRQE</a> </p></li></ul><h3 class="heading" style="text-align:left;" id="5-regulatory-updates">5. Regulatory Updates</h3><p class="paragraph" style="text-align:left;"><b>Title</b>: Navigating New FDA Regulations</p><ul><li><p class="paragraph" style="text-align:left;"><b>Summary</b>: Key changes in FDA regulations and what they mean for your organization. The FDA has recently updated its guidelines on the approval process for cell and gene therapies, aiming to streamline the pathway for innovative treatments.</p></li><li><p class="paragraph" style="text-align:left;"><b>Read More</b>: <a class="link" href="https://www.fda.gov/vaccines-blood-biologics/biologics-guidances/cellular-gene-therapy-guidances?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-august-2024" target="_blank" rel="noopener noreferrer nofollow">here</a> and <a class="link" href="https://www.aabb.org/news-resources/news/article/2024/04/30/regulatory-update--fda-issues-draft-guidances-related-to-cell-and-gene-therapy?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-august-2024" target="_blank" rel="noopener noreferrer nofollow">here</a>.</p></li></ul><h3 class="heading" style="text-align:left;" id="6-case-study">6. Case Study</h3><p class="paragraph" style="text-align:left;"><b>Title</b>: Success Story: AI-Discovered Clinical Oncology Programs</p><ul><li><p class="paragraph" style="text-align:left;"><b>Summary</b>: How one startup Iambic Therapeutics leveraged innovative solutions to achieve significant milestones. Focusing on personalized cancer therapies Iambic Therapeutics successfully raised $150 million in Series B funding and achieved promising results in early clinical trials including IAM1363, a highly selective, brain penetrant small molecule inhibitor.</p></li><li><p class="paragraph" style="text-align:left;"><b>Read More</b>: <a class="link" href="https://www.businesswire.com/news/home/20240618665195/en/Iambic-Therapeutics-Closes-50-million-Series-B-Extension-to-Broaden-its-Pipeline-of-AI-Discovered-Clinical-Oncology-Programs?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-august-2024" target="_blank" rel="noopener noreferrer nofollow">Link to full article</a></p></li></ul><h3 class="heading" style="text-align:left;" id="6-case-study">7. Resources</h3><p class="paragraph" style="text-align:left;"><b>Title</b>: Access and download resources from our site</p><ul><li><p class="paragraph" style="text-align:left;"><a class="link" href="https://knowledgeessentials.eleapcourses.com/v7/computer-system-validation-fda-warning-letters-case-studies-lessons-learned-174386.html?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-august-2024" target="_blank" rel="noopener noreferrer nofollow">Computer System Validation – FDA Warning Letters Case Studies – Lessons Learned</a></p></li><li><p class="paragraph" style="text-align:left;"><a class="link" href="https://knowledgeessentials.eleapcourses.com/v7/the-gamp-approach-to-21-cfr-part-11-compliance-148301.html?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-august-2024" target="_blank" rel="noopener noreferrer nofollow">The GAMP Approach to 21 CFR Part 11 Compliance</a></p></li><li><p class="paragraph" style="text-align:left;"><a class="link" href="https://quality.eleapsoftware.com/resources/?utm_source=eleapcompliance.com&utm_medium=newsletter&utm_campaign=this-week-in-compliance-august-2024" target="_blank" rel="noopener noreferrer nofollow">SOP Templates</a></p></li></ul></div><div class='beehiiv__footer'><br class='beehiiv__footer__break'><hr class='beehiiv__footer__line'><a target="_blank" class="beehiiv__footer_link" style="text-align: center;" href="https://www.beehiiv.com/?utm_campaign=461d8862-260e-4188-b948-3c1bbbbf6074&utm_medium=post_rss&utm_source=eleap_compliance">Powered by beehiiv</a></div></div>
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