CAPA Management: Technology to the Rescue April 18, 2023 If you have been struggling with corrective and preventive action (CAPA) management, it’s possible there is a tech solution that will lift the burden. CAPA technology helps streamline the process by automating many of the manual tasks involved in the corrective action process. For example, it can automate the following tasks: Issue Tracking: It can provide a centralized repository for tracking quality issues, allowing teams to see the status of corrective actions and prioritize their efforts. Workflow Management: CAPA technology can automate the workflow of the corrective action process, from the identification of an issue to the implementation of the corrective action and follow-up. This helps to ensure that all steps are taken in a timely manner and that nothing falls through the cracks. Notifications and Reminders: Software can send automated notifications and reminders to relevant stakeholders, ensuring that everyone is aware of their responsibilities and deadlines. This helps to keep the corrective action process moving forward and reduces the risk of delays. Data Collection and Analysis: CAPA tech solutions can automate the collection and analysis of data, such as production data, customer complaints, and field returns. This data can be used to identify potential quality issues and ensure that corrective actions are taken in a data-driven, evidence-based manner. Verification and Validation: It can automate the follow-up and verification process, ensuring that corrective actions have been effective in preventing the issue from recurring. By automating these tasks, CAPA technology helps to reduce the time and resources required to complete the corrective action process, making it more efficient and effective. This allows quality managers to focus on more strategic tasks, such as analyzing data and developing continuous improvement initiatives. Additionally, the centralized repository and real-time data provided by CAPA technology can help organizations to make informed, data-driven decisions about their quality management processes. Share via: Twitter LinkedIn Facebook Email
EVENT 7th Annual European Medical Device & Diagnostic Quality Assurance and Regulatory Affairs Conference Unlock tomorrow's standards today: Innovate, collaborate, and lead at the Quality Assurance and Regulatory Affairs Conference! The 7th Annual European Medical Device and Diagnostic Supplier Quality Management Conference aims to bring together the industry’s top-performing Supplier Quality Management (SQM) & QA QC professionals under one roof. Distinguished speakers will discuss cutting-edge strategies and procedures for meeting regulatory SQM & QMS requirements, implementing risk-based approaches, minimizing the risk of quality failures, and linking QA QC processes throughout the product life cycle. This two-day in-person conference will provide attendees with live content and highly interactive sessions supported by real-life business examples, case studies, Q&A sessions, panel debates, and interactive workshops. You’ll be able to network with your peers, including leading technology innovators and service providers, while exchanging ideas with the experts in a collaborative setting. We are Bronze Sponsors of the 2024 Medical Device QA & SQM Conference in Belgium. Learn more
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WEBINAR Discover How Gedeon Richter Transformed Their Quality Management Hear how leading European Pharmaceutical and Biotech company Gedeon Richter successfully implemented a digital quality management system to support their business goals and patient-centric mission. Learn more
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EVENT Honeywell Life Sciences Innovation Days Honeywell invites you to join us for one of our Life Sciences Innovation Days, a series offered throughout the globe in 2024. We will present a variety of process innovations to support the digital transformation of life sciences manufacturing. Themes will include orchestrating systems and data, preventing and containing cyber incidents, quality control and management, modular automation, and the Honeywell life sciences roadmap. Discussion will address streamlining manufacturing, creating batch records, and fulfilling regulatory reporting requirements. Learn more
EVENT Pharma Manufacturing World Summit Join us at Pharma Manufacturing World Summit on May 14, 2024 where Honeywell's Zillery Fortner will be co-presenting on "The Value of a Unified Life Sciences Solution in Pharma 4.0." Learn more
EVENT TUG Europe Join industry peers at one of these FREE events for TrackWise and TrackWise Digital customers, with two dates and locations to choose from. Enjoy a networking at our pre-event receptions, as we celebrate 30 years of TrackWise! Take advantage of a FREE TrackWise Digital pre-event training workshop. Learn more
EVENT RQA 2024: International QA Conference With diverse industry representation including regulatory authorities like the MHRA, it’s a hotspot for those in GCP, GLP, GMP, pharmacovigilance, and more. The conference has evolved to cover a wider scope, offering unparalleled networking opportunities across three dynamic days for delegates, sponsors, and exhibitors to engage on pivotal industry topics. Register to attend this insightful event where you can hear our Industry Business Development Director, Fabrizio Mangilio deliver one of this year's RQA 2024 keynote sessions. We are Platinum Sponsors of the RQA 2024: International QA Conference Learn more
EBOOK 5 Things to Know About EUDAMED EUDAMED (European database for medical devices) is a centralized database that aims to enhance the transparency and traceability of medical devices in the EU. Learn more
WEBINAR EUDAMED 2024 and Beyond: Preparing for the Future of Medical Device Oversight Watch our on-demand webinar and gain valuable insights into the transformative impact of EUDAMED on the Medical Device industry. Learn more
WHITE PAPER Future-Proofing a Pharma Manufacturing Legacy through Digital Quality Transformation As industries adopt technological advances and rapidly move into the fourth industrial revolution, it is essential to assess the impact of these isolated data pockets on the workforce, customers and the safety of patients. Learn more
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