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| Skip to content * Services Show submenu for {{ link.label }} + Quality Assurance + Global Supplier Audit Support + Regulatory Affairs + Clinical Affairs + Technical Consulting Services + Talent Acquisition * Industries Show submenu for {{ link.label }} + Medical Devices + Pharmaceutical + Biotechnology + Diagnostics + CLIA Labs + Food + Agriculture * About Us * Resources Show submenu for {{ link.label }} + FAQ + Blog + Case Studies + Digital Brochure + Glossary * Contact Us Show submenu for {{ link.label }} + Request a Quote Open main navigation Close main navigation * Services Show submenu for {{ link.label }} + Quality Assurance + Global Supplier Audit Support + Regulatory Affairs + Clinical Affairs + Technical Consulting Services + Talent Acquisition * Industries Show submenu for {{ link.label }} + Medical Devices + Pharmaceutical + Biotechnology + Diagnostics + CLIA Labs + Food + Agriculture * About Us * Resources Show submenu for {{ link.label }} + FAQ + Blog + Case Studies + Digital Brochure + Glossary * Contact Us Show submenu for {{ link.label }} + Request a Quote * Get Started Now Get Started Now The Medpoint Blog Learn best practices and gain new insights on quality assurance, regulatory strategy, and clinical affairs. Beyond the Metals Tariffs: Hidden Costs in Medical Devices July2025 On June 4, 2025, the United States raised the global tariff on aluminum and steel from 25% to 50%, w... Read more Unlocking the Power of Collaboration – The Key to Inspection Readiness May2025 In the highly regulated world of the pharmaceutical and medical device industries, a buzzword that h... Read more FDA Releases New Guidance on Weight-Reduction Medications: A Comprehensive Overview April2025 In January 2025, the FDA released a draft guidance titled Obesity and Overweight: Developing Drugs a... Read more Understanding the ISO 9001 Climate Change Amendment: What it Means for Certified Organizations March2025 The role of ISO 9001 in quality management is to provide a standardized framework for Quality Manage... Read more The Underappreciated Science of Soft Skills in Medical Device Audits: Insights from Andy Nichols January2025 Medical device audits are vital for ensuring compliance, maintaining quality, and safeguarding patie... Read more Post-Pandemic Lessons on Supply Chain Vulnerabilities January2025 The COVID-19 pandemic exposed significant vulnerabilities in global supply chains, challenging long-... Read more FDA’s New Draft Guidance on Clinical Trial Diversity: What Sponsors Need to Know November2024 Read more Cutting Costs or Cutting Corners? The True Cost of Skipping Supplier Audits. October2024 Read more QMSR: Harmonizing 21CFR820 & ISO 13485 – What is the impact on industry? August2024 The medical device industry operates under a complex web of regulations, with 21 CFR Part 820, commo... Read more How Does Quality Culture Contribute to Compliance? August2024 Creating a quality culture within the workplace is foundational to quality compliance. The keystones... Read more Subscribe Here! Recent Posts Beyond the Metals Tariffs: Hidden Costs in Medical Devices Unlocking the Power of Collaboration – The Key to Inspection Readiness FDA Releases New Guidance on Weight-Reduction Medications: A Comprehensive Overview Post tags * Regulatory Affairs * FDA Regulations * Medical Device * Audits * Technical Advising * Pharmaceutical * Medpoint Company News * QMS- Quality Management System * Biotechnology * Clinical Strategy First Prev 1 2 3 4 5 Next Last We strive to partner with medical device, pharmaceutical, and biotechnology companies to achieve and maintain global compliance in the areas of quality assurance, regulatory, and clinical affairs. 844-MEDPOINT info@medpoint.com * Home * Industries * About Us * Resources * Contact Us Subscribe to our Blog We strive to partner with medical device, pharmaceutical, and biotechnology. © 2026 Medpoint, LLC. All rights reserved. Privacy Policy | Cookie Policy | Skip to content * Services Show submenu for {{ link.label }} + Quality Assurance + Global Supplier Audit Support + Regulatory Affairs + Clinical Affairs + Technical Consulting Services + Talent Acquisition * Industries Show submenu for {{ link.label }} + Medical Devices + Pharmaceutical + Biotechnology + Diagnostics + CLIA Labs + Food + Agriculture * About Us * Resources Show submenu for {{ link.label }} + FAQ + Blog + Case Studies + Digital Brochure + Glossary * Contact Us Show submenu for {{ link.label }} + Request a Quote Open main navigation Close main navigation * Services Show submenu for {{ link.label }} + Quality Assurance + Global Supplier Audit Support + Regulatory Affairs + Clinical Affairs + Technical Consulting Services + Talent Acquisition * Industries Show submenu for {{ link.label }} + Medical Devices + Pharmaceutical + Biotechnology + Diagnostics + CLIA Labs + Food + Agriculture * About Us * Resources Show submenu for {{ link.label }} + FAQ + Blog + Case Studies + Digital Brochure + Glossary * Contact Us Show submenu for {{ link.label }} + Request a Quote * Get Started Now Get Started Now The Medpoint Blog Learn best practices and gain new insights on quality assurance, regulatory strategy, and clinical affairs. Beyond the Metals Tariffs: Hidden Costs in Medical Devices July2025 On June 4, 2025, the United States raised the global tariff on aluminum and steel from 25% to 50%, w... Read more Unlocking the Power of Collaboration – The Key to Inspection Readiness May2025 In the highly regulated world of the pharmaceutical and medical device industries, a buzzword that h... Read more FDA Releases New Guidance on Weight-Reduction Medications: A Comprehensive Overview April2025 In January 2025, the FDA released a draft guidance titled Obesity and Overweight: Developing Drugs a... Read more Understanding the ISO 9001 Climate Change Amendment: What it Means for Certified Organizations March2025 The role of ISO 9001 in quality management is to provide a standardized framework for Quality Manage... Read more The Underappreciated Science of Soft Skills in Medical Device Audits: Insights from Andy Nichols January2025 Medical device audits are vital for ensuring compliance, maintaining quality, and safeguarding patie... Read more Post-Pandemic Lessons on Supply Chain Vulnerabilities January2025 The COVID-19 pandemic exposed significant vulnerabilities in global supply chains, challenging long-... Read more FDA’s New Draft Guidance on Clinical Trial Diversity: What Sponsors Need to Know November2024 Read more Cutting Costs or Cutting Corners? The True Cost of Skipping Supplier Audits. October2024 Read more QMSR: Harmonizing 21CFR820 & ISO 13485 – What is the impact on industry? August2024 The medical device industry operates under a complex web of regulations, with 21 CFR Part 820, commo... Read more How Does Quality Culture Contribute to Compliance? August2024 Creating a quality culture within the workplace is foundational to quality compliance. The keystones... Read more Subscribe Here! Recent Posts Beyond the Metals Tariffs: Hidden Costs in Medical Devices Unlocking the Power of Collaboration – The Key to Inspection Readiness FDA Releases New Guidance on Weight-Reduction Medications: A Comprehensive Overview Post tags * Regulatory Affairs * FDA Regulations * Medical Device * Audits * Technical Advising * Pharmaceutical * Medpoint Company News * QMS- Quality Management System * Biotechnology * Clinical Strategy First Prev 1 2 3 4 5 Next Last We strive to partner with medical device, pharmaceutical, and biotechnology companies to achieve and maintain global compliance in the areas of quality assurance, regulatory, and clinical affairs. 844-MEDPOINT info@medpoint.com * Home * Industries * About Us * Resources * Contact Us Subscribe to our Blog We strive to partner with medical device, pharmaceutical, and biotechnology. © 2026 Medpoint, LLC. All rights reserved. Privacy Policy | Cookie Policy |
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