GxP Training : #1 Certified Online Courses Provider for Life Sciences Professionals

🛡️ Keep your entire team certified, compliant and audit-ready with GxP Training. One catalog of certified courses covering GMP, GCP, GLP, GDP, pharmacovigilance, medical devices, regulatory affairs and AI. From preclinical development to post-marketing. Everything your team needs to stay audit-ready: 👥 Enroll up to 5,000 employees in one click 📊 One dashboard for every score, certificate and completion 📋 Audit-ready training records, generated automatically 🏅 21 CFR Part 11 compliant certificates with CPD/CEU credits 🔗 SCORM files to host in your own LMS 🧪 Custom courses built by our GxP experts The auditor asks for your training records. You already have them. ✅ 👉 Swipe to see how it works, then request a demo: https://lnkd.in/etzD4dbJ #GxP #GMP #QualityAssurance #LifeSciences #Compliance

🎉 New Course: ISO 9001:2026 Quality Management Systems ISO 9001:2015 is history. From now, ISO 9001:2026 is the standard that counts for auditors. This is the first full revision in eleven years. Every certificate must move by September 2029, and auditors will run out before the deadline. Five clauses changed: quality culture and ethics, climate change, policy tied to strategy, risks split from opportunities, wider awareness. Everything else is clarification. Our new ISO 9001:2026 course gets quality, regulatory and audit teams ready: understand, apply, transition. ✅ What you'll learn: * Spot the five real changes and the clarifications that only look like changes * Run PDCA and risk-based thinking an auditor can trace * Prove quality culture, integrity and ethical behavior at the top * Separate risks from opportunities and verify every planned change * Build a gap analysis and transition plan that passes the first 2026 audit Every lesson ends with what auditors look for. Eight real cases, from Kobe Steel to Philips Respironics. 👨🔬👩🔬 Who should enroll? QA and QC teams, regulatory and compliance specialists, internal auditors and process owners in pharma, medical devices, laboratories and their suppliers. 🏅 Your Reward? A worldwide recognized certificate, traceable and shareable on LinkedIn, with compliance validation via our online checker in case of audit. And CPD/CEU Credits. 👇 This course includes real-life examples, scenario-based quizzes, and a final exam to validate your knowledge. Enroll here: https://lnkd.in/ePeRqGkh #ISO9001 #QualityManagement #QMS #QualityAssurance #Pharma #MedicalDevices #GxP #LifeSciences

🎉 New Course: The Common Technical Document: CTD and eCTD (ICH M4 and M8) ICH M4 sets the one format every medicines regulator expects: five modules, one dossier, mandatory in its electronic eCTD form at the FDA and the EMA. One broken hyperlink or one checksum mismatch and your submission is refused at the technical gate, before anyone reads the science. Stop losing weeks to format errors. Learn to build, validate and submit a dossier that passes the gate the first time. Our new CTD and eCTD course helps regulatory affairs, CMC and clinical teams structure, publish and validate a compliant dossier with confidence. ✅ What you'll learn: * Place every quality, safety and efficacy document in the right CTD module * Tailor Module 1 to the US, the EU and Japan without touching the shared core * Build, sequence and update an eCTD with the XML backbone and four lifecycle operations * Pass technical validation and avoid the errors that get submissions refused Anticipate what comes next, from eCTD v4.0 to IDMP 👨🔬👩🔬 Who should enroll? Regulatory affairs associates and officers, submission publishing teams, CMC, nonclinical and clinical specialists who feed the dossier, and quality teams maintaining it after approval. One shared method, so the dossier passes the gate the first time. 🏅 Your Reward? A worldwide recognized certificate, traceable and shareable on LinkedIn, with compliance validation via our online checker in case of audit. And CPD/CEU Credits. 👇 This course includes real-life examples, scenario-based quizzes, and a final exam to validate your knowledge. Enroll here: https://lnkd.in/eqVz_NmZ #CTD #eCTD #RegulatoryAffairs #ICH #RegulatorySubmissions #Pharma #DrugDevelopment #GxPTraining

🎉 New Category: Artificial Intelligence for Life Sciences Your teams already use ChatGPT, Claude and Copilot at work, and most were never trained. FDA, EMA and the EU AI Act now expect proof that your people use AI responsibly. One bad prompt is an audit finding. That is why we opened a new category with 3 certified courses dedicated to AI and more to come... ✅ The 3 new AI courses: * Practical AI for Healthcare and Pharma * AI Compliance in Life Sciences * EU AI Act for Pharmaceuticals and Medical Devices Take one, or all three: use the tools, build the program, know the rules. 👨🔬👩🔬 Who should enroll? Quality assurance, regulatory affairs, clinical operations, pharmacovigilance, IT/CSV validation and data management professionals, plus anyone in a regulated role who opens an AI assistant during the working day. 🏅 Your Reward? A worldwide recognized certificate, traceable and shareable on LinkedIn, with compliance validation via our online checker in case of audit. And CPD/CEU Credits. 👇 Each course includes real-life examples, scenario-based quizzes, and a final exam to validate your knowledge. Swipe through the carousel for the details. Explore the AI courses: https://lnkd.in/eFnEC4Vs #ArtificialIntelligence #AICompliance #EUAIAct #GenerativeAI #Pharma #MedicalDevices #QualityAssurance #LifeSciences

🎉 New Course: The Decentralised Procedure (DCP) One dossier. One Reference Member State. 27 markets. 210 days. That is the Decentralised Procedure under Directive 2001/83/EC, and it is unforgiving: one failed validation or one unresolved objection sends your file to CMDh referral, then arbitration, and your European launch slips by a year. Our new Decentralised Procedure (DCP) course helps regulatory affairs, CMC, clinical and quality professionals run the procedure with confidence. ✅ What you'll learn: * Choose between the DCP and the MRP * Pick the right Reference Member State * Submit a dossier that passes validation * Run the Day 0 to Day 210 timeline * Handle CMDh referral and arbitration 👨🔬👩🔬 Who should enroll? Regulatory affairs officers and submission teams, CMC, clinical and pharmacovigilance specialists, project managers choosing between European routes, and quality teams maintaining authorisations after approval. 🏅 Your Reward? A worldwide recognized certificate, traceable and shareable on LinkedIn, with compliance validation via our online checker in case of audit. And CPD/CEU Credits. 👇 This course includes real-life examples, scenario-based quizzes, and a final exam to validate your knowledge. Enroll here: https://lnkd.in/eUjsEXki

🎉 New Course: EU AI Act for Pharmaceuticals and Medical Devices In August 2026, the EU AI Act will be applied in each member state in Europe, and compliance is mandatory. Most AI in pharma and medical devices is classified high-risk, with its core obligations applying from August 2026. You could face fines up to €35 million or 7% of global turnover, refused CE marking and product withdrawal. Our new EU AI Act for Pharmaceuticals and Medical Devices course gives regulatory, quality and AI teams a clear method to meet every requirement and prove it in an audit. ✅ What you'll learn: * Classify any AI system into the correct risk tier under Article 6 * Apply the seven core requirements for high-risk AI under Articles 9 to 15 * Map the duties of providers, deployers, importers and distributors * Align the Act with the MDR, IVDR, GxP and data integrity expectations * Build a conformity file and CE marking that pass EU inspection 👨🔬👩🔬 Who should enroll? Regulatory affairs, quality assurance, AI and data science owners, medical device and IVD manufacturers, and clinical, pharmacovigilance and manufacturing leaders deploying AI in regulated environments. 🏅 Your Reward? A worldwide recognized certificate, traceable and shareable on LinkedIn, with compliance validation via our online checker in case of audit. And CPD/CEU Credits. 👇 This course includes real-life examples, scenario-based quizzes, and a final exam to validate your knowledge. Enroll here: https://lnkd.in/eBJ-YMPe #EUAIAct #ArtificialIntelligence #MedicalDevices #Pharmaceuticals #RegulatoryAffairs #AICompliance #LifeSciences