Partnership for Public Service’s Post

Navigating the DPDPA: The Act's impact on the rapidly growing ed-tech industry presents challenges but also significant opportunities for trust, innovation, and global alignment. Discover what ed-tech institutions need to follow and how they can leverage this opportunity. Explore this in our latest blog. Read the full blog here: https://lnkd.in/gffFer95 #EdTech #DataProtection #DPDPA #Compliance #Innovation

Don't miss this intriguing series about how industry leaders utilize Artificial Intelligence, presented by our Innovative Technology Action Group - ITAG! Learn more at: https://lnkd.in/eCnU4j4X #ArtificialIntelligence #AI #Technology #ChesterCounty

Let's coordinate for efficiency and compliance. Can we obtain regulatory exemptions for greater efficiency? Let's talk about it in upcoming virtual workshop - attend this 1 hour webinar hosted by Wayne Dunnington - sign up today! https://lnkd.in/gK9bDrMk #doingitright

There's a BRAND NEW episode of Pathways to Success - Conversations with Clinical Experts out! In this episode, Karen Welsh, VP of Clinical & Reimbursement Excellence, is joined by George Douaire, CEO of Stride Tech Medical, Inc., to discuss the role of technology in patient care, regulatory issues, and much more! Watch the full episode below!

The FDA's recently released IT Operating Plan outlines a strategic roadmap for modernizing the agency's technology infrastructure and operations. This plan emphasizes transparency, collaboration, and accountability, all of which are crucial for ensuring the safety and efficacy of FDA-regulated products. As a leading provider of Quality Management software, ACCELQ can play a significant role in helping the FDA achieve its IT Operating Plan goals in several key areas: Boost Efficiency and Speed Accelerate Test Automation: Say goodbye to #manualtesting bottlenecks. ACCELQ automates a wide range of #tests , from #ui to #api , freeing up resources for higher-level activities. Continuous Integration & Delivery (CI/CD): Seamlessly integrate ACCELQ into your #cicd pipeline for rapid, #automatedtesting with every code change, ensuring early defect detection and faster releases. Enhance Regulatory Compliance Pre-Built Compliance Libraries: Simplify adherence to 21 CFR Part 11 and other regulations with built-in compliance checks and audit trails. Data Integrity: Maintain pristine data integrity with robust version control, traceability, and tamper-proof audit trails. Improve Software Quality AI-powered Test Case Generation: Generate comprehensive test cases automatically with AI, covering a wider range of scenarios and edge cases. Smart Test Execution: Optimize test execution based on risk and impact, prioritizing critical areas and maximizing test coverage. Empower Collaboration: Centralized Platform: Consolidate testing efforts across teams and projects for improved visibility, collaboration, and knowledge sharing. Real-time Reporting & Analytics: Gain real-time insights into test results, defect trends, and team performance, facilitating data-driven decision-making. Specific Examples: Streamline Medical Device Software Testing: Automate complex medical device testing with pre-built modules for specific functionalities, ensuring compliance and safety. Modernize Clinical Trial Platform Testing: Quickly test and validate clinical trial platforms with ACCELQ's no-code approach, accelerating research and development. Strengthen Internal Applications: Ensure the stability and security of internal FDA applications through comprehensive, automated testing. The ACCELQ Advantage: Cloud-based and Scalable: Easily scale testing efforts to meet evolving needs and ensure seamless collaboration across distributed teams. Intuitive and No-code: Empower everyone, regardless of coding expertise, to contribute to the testing process, democratizing quality assurance. Proven Success: Trusted by leading healthcare and life sciences organizations to deliver high-quality, compliant software. By partnering with ACCELQ, the FDA can achieve its IT Operating Plan goals in software development and testing, ultimately delivering safer, more effective medical products to the public. #ACCELQ #FDA #ITOperatingPlan #qualitymanagement #AI #softwaredevelopment 🚀💻

Fish’s 2023 Post-Grant Report takes a deep dive into the cases, trends, and statistics that shaped post-grant practice throughout the year and how they might affect practitioners going forward. https://lnkd.in/gdCDwmJ7 #FishRichardson #PTAB 

The Biden Administration opened a public comment period for its Draft Interagency Guidance Framework for Considering the Exercise of March-in Rights. This advisory outlines the new framework's potential implications on drug pricing, university-industry technology transfer, and federally funded intellectual property more broadly. #BayhDole #MarchInRights #techtransfer #drugpricing #intellectualproperty

We published the FDA IT strategy last year with the promise of an IT Operating plan which would provide details of the actions underway to deliver on the strategy. As we tune future initiatives via the lens of the strategy and priorities, we expect to see much tighter alignment with mission goals and business priorities.

📣 The next instalment of our TLT #TechKnow series from my colleagues Louisa Williams and Lauren Shinfield is out! Discussing Labour's plans for the new Digital Information and Smart Data Bill and how that is different (and not so different!) from the previous Government's plans. Well worth a watch! #TechKnow #Data #DataProtection #Datalawyers #DataLaw #TLT #ForWhatComesNext

Check out the latest blog post on the history of technology: "The Real Reason LaserDisc Failed Spectacularly." Learn about the rise and fall of this unique technology and why it ultimately didn't succeed. Gain valuable insights into the world of digital media by reading the full article here: https://ift.tt/UMcaoml