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

New Certified Training: Laboratory Management Systems - ISO/IEC 17025:2017 🔬 The ISO/IEC 17025:2017 framework is crucial for any laboratory performing testing and calibration, offering a reliable protocol to ensure precise and trustworthy results. 👨🔬👩🔬 Who Should Enroll?  Perfect for QC lab analysts, pharmaceutical engineers, biotech researchers, quality assurance specialists, and laboratory managers. 📚 What Will You Learn? 👉 Understand the comprehensive structure of ISO/IEC 17025:2017 👉 Grasp the importance of impartiality and confidentiality in laboratory operations 👉 Learn the steps to achieve accreditation and understand the role of accreditation bodies, ensuring labs meet international standards. 👉 Master the documentation and management system requirements to improve operational quality and achieve consistent results. 👉 And much more! ✅ Practical Applications The tragic Therac-25 accidents in the 1980s, due to software faults in radiation therapy machines, highlight the life-saving importance of adhering to standards like ISO/IEC 17025:2017 for ensuring safety and reliability in medical testing and calibration. 🎓 A Unique Certification? Upon completing this course, you will receive a Certificate of Completion, widely recognized in over 45 countries. Proudly showcase your achievement on LinkedIn, and rest assured that its authenticity can be easily validated in case of audit through our online certificate checker tool. 🌐 Interactive Learning Online Engage with practical case studies and quizzes that reinforce your understanding throughout the course. Interested? Enroll now! https://lnkd.in/dvQX2-qw #labs #laboratorymanagementsystems #onlinecourse #certification

New Certified Training: 21 CFR Part 58 GLP: Good Laboratory Practice for Nonclinical Laboratory Studies This certified course offers a thorough understanding of the Good Laboratory Practice (GLP) principles as outlined in 21 CFR Part 58, which are crucial for the integrity and reliability of nonclinical laboratory studies. These guidelines are essential for any facility engaged in preclinical research, providing a structured approach to ensure data integrity and compliance with FDA regulations. Equip your team with the knowledge needed to uphold the highest standards in nonclinical trial testing. 👨🔬👩🔬 Who Should Enroll? Perfect for biomedical scientists, regulatory affairs specialists, laboratory technicians, pharmacists, and compliance officers, this course offers comprehensive insights into understanding and implementing GLP standards in nonclinical laboratory environments. 📚 What Will You Learn? - Grasp the importance of Good Laboratory Practices (GLP) in nonclinical laboratories. - Understand the comprehensive aspects of 21 CFR Part 58 GLP regulations. - Explore best practices for facility and equipment management under GLP standards. - Gain insights into documentation and reporting requirements in GLP compliance. And much more! ✅ Practical Applications The 1970s' data falsification issues at Industrial Bio-Test Laboratories highlighted the essential need for the 21 CFR Part 58 regulations to ensure integrity and reliability in nonclinical research through rigorous Good Laboratory Practices, safeguarding public health. 🎓 A Unique Certification? Upon course completion, you'll earn a prestigious certificate, backed by globally acknowledged CPD/CEU credits. This certificate is distinct, easily shareable on LinkedIn, and can be verified using our online certificate tracking system. 🌐 Experience Interactive Learning Online Engage with practical case studies and quizzes that reinforce your understanding throughout the course. Interested? Enroll now! 👇🏼

New Certified Training : Good Clinical Laboratory Practice (GCLP) 🔬 This new certified course offers a comprehensive understanding of the quality system framework necessary for the analysis of clinical trial samples, ensuring all laboratory processes and results meet GCLP standards. GCLP is a set of guidelines essential for any organization involved in the analysis of samples from Clinical Trials, ensuring compliance with Good Clinical Practice (GCP) requirements. 👨🔬👩🔬 Who Should Enroll? Perfect for Sponsors, Laboratory Managers, Project Managers, Clinical Research Associates (CRAs), and Quality Assurance Personnel, this course covers everything you need to know about maintaining compliance with GCLP standards. 📚 What Will You Learn? - Understand the key differences between GCP, GLP, and GCLP. - Learn the principles of GCLP, including organization, personnel, and quality control. - Develop comprehensive Clinical Trial Protocols and Analytical Plans. - Master effective methods for sample management and data integrity. - And much more! 🎓 A Unique Certification? After completing the course you'll receive an internationally recognized certificate, endorsed by CPD/CEU credits. Each certificate is unique, shareable on Linkedin and traceable thanks to our online certificate checker. 🌐 Experience Interactive Learning Online Engage with practical case studies and quizzes that reinforce your understanding throughout the course. Interested? Enroll now ! https://lnkd.in/d2FTxugK #clinicaltrials #gclp #gcp #onlinecourse #certification

🚨 In light of the FDA’s recent crackdown on GMP non-compliance, the importance of rigorous GMP training and certification has soared in case of audit. Our latest guide highlights essential trainings that not only ensure compliance but also advance your organization’s quality standards. Whether you're in pharmaceuticals, food safety, medical devices, or cosmetics, proper certification through targeted training is crucial. GxP Training issued certificates are unique and traceable. They can be verified during audits or inspections through our online certificate checker. 👍 https://lnkd.in/de9rr92Z #GMP #Compliance #QualityAssurance #AuditSuccess #Certification #ProfessionalDevelopment

🚀 Exciting News for Medical Device Professionals! 🚀 Are you looking to master the complexities of risk management and enhance patient safety in medical device manufacturing? Our new certified course, "Risk Management for Medical Devices," is exactly what you need! 👨🔬👩🔬 Who Should Enroll?   Ideal for Quality Managers, Regulatory Affairs Specialists, and development team members, this course dives deep into the ISO 14971 standard, ensuring you’re equipped to maintain the highest standards of product safety and efficacy. 📚 What Will You Learn? - Utilize the 5X5 Matrix for effective risk assessment.   - Develop and implement robust Risk Management Policies and Plans.   - Master the use of FMEA in risk management processes.   - Conduct thorough risk analyses to identify and mitigate potential hazards.   - And much more! 🎓 Your Takeaway? An internationally recognized GxP Training certificate, FDA / EMA compliant, traceable, complete with CPD/CEU credits, and the confidence to share it on Linkedin. 🌐 Experience Interactive Learning Online** Enjoy engaging content with case studies and quizzes designed to reinforce your learning throughout the course. Interested? Enroll now ! https://lnkd.in/enY7PX9b Let’s elevate the standards of safety and efficacy together! 💪 #medicaldevices #training #certification #onlinecourse #compliance #regulatory

🚨 New course : How to write SOPs for ISO standards ! Are you a quality manager, compliance officer, or involved in ensuring your organization meets ISO certification standards? Our Certified Course on Writing Effective SOPs is tailor-made for you! This certified course is designed to guide you through the intricate process of developing, managing, and optimizing SOPs. 📚 Course Highlights: - The lifecycle of an SOP - The control and management of SOPs - Practical tips for creating concise, one-page procedures - Strategies for managing procedures in complex or cross-departmental processes Don't miss this opportunity to certify your skills and advance your career in quality and compliance. Enroll today 🤩 #Certification #QualityManagement #ISOcertification #SOPs #Compliance #ProfessionalGrowth https://lnkd.in/d5-_CvCA

Ever heard of the massive scandals like Enron ? 🚀 We're dropping our latest gem: the Anti-Bribery and Anti-Corruption: ISO37001 Certified Course. In the wake of increasing global scrutiny, safeguarding your operations against bribery and corruption isn’t just ethical—it’s mandatory. Achieving ISO 37001 certification signals your unwavering commitment to integrity and excellence in all business practices. Course Highlights: * Expert-led insights by Josh Harrison, our seasoned Anti-Corruption and ISO Consultant with over 20 years of experience. *A deep dive into the historical background, framework, and structure of the ISO 37001:2016 standards. * Practical knowledge for the establishment, review, and management of an effective Anti-Bribery Management System (ABMS). Who Should Enroll ? This course is ideal for ALL professionals in life sciences, external and internal auditors, and anyone involved in or aspiring to specialize in anti-bribery management systems. Upon completion, earn a downloadable, traceable, and CPD/CEU accredited Certificate of Completion that’s 21 CFR PART 11 compliant, verifiable online, and shareable on LinkedIn. Ready ? Enroll now below 👇🏼 https://lnkd.in/dERvjVuN #compliance #antibribery #anticorruption #iso37001 #ethicalbusiness #certifiedtraining

🌟 New course : ISO 13485:2016 Internal Auditor 🌟 This certified online course is designed for people working in medical devices : Quality Assurance Managers, Regulatory Affairs Specialists, and Quality Systems Engineers. 📚 Course Curriculum Highlights: - Introduction & Overview of ISO 13485:2016 - Lesson 1: Quality Management System - Lesson 2: Management Responsibility - Lesson 3: Resource Management - Lesson 4: Product Realization - Lesson 5: Measurement, Analysis, and Improvement - Glossary & Evaluation 🚀 Meet Your Instructor: Dr. Ciaran McEnister, a Senior Pharmaceutical Executive with over 25 years of experience, is at the helm of this course. His extensive background in Medical Device Development, Regulatory Compliance, and Quality Management, having served as a senior quality manager at renowned organizations such as Merckx, BioDevices, and IPSEN, brings invaluable insights and practical knowledge to the curriculum. 🏆 Certification: Achieve a traceable, uniquely numbered certificate of completion that stands as a testament to your updated auditing capabilities. This print-ready certificate, downloadable as a PDF, is a significant credential for your professional growth. Embark now on this journey to excellence with us 👇🏼 #MedicalDevice #QualityAssurance #InternalAuditor #ISO13485 #ProfessionalDevelopment #Certification #Leadership https://lnkd.in/dVXTuVQB

🌟 New: Clinical Research Associate (CRA) Certified Training Bundle 🌟 The landscape of clinical research is ever-evolving, and staying ahead requires not just knowledge, but deep, actionable insight. Our Clinical Research Associate Certified Bundle is your gateway to mastering the complexities of clinical trials and ensuring your compliance. 👩🔬 Who Should Enroll? - Clinical Research Associates (CRAs) - CRA Managers - Human Resources Specialists in Clinical Research - Quality Assurance and Quality Control Professionals in Pharma - Operational Staff and Production Managers aiming to branch into clinical research 👩🏫 Learn from the Best: Dr. Patricia Kay, with her extensive experience at Pfizer, GSK, and AstraZeneca, leads this program. Her practical approach ensures you gain skills that are not just academic but directly applicable to your day-to-day challenges in clinical research. 📚 What's in the Bundle? 1) ICH-GCP Training Refresher 2024 2) Introduction to Clinical Trial Protocols 3) Clinical Data Management 4) Management of Clinical Study Reports 5) Management of The TMF and ISF 6) Global Pharmacovigilance Awareness 🏅 Get Certified: Each course within the bundle leads to a unique, verifiable certificate, CPD/CEU accredited and FDA 21 CFR PART 11 compliant. Upon completion of the path, receive a unique and traceable certification 📈 Take Your Career to New Heights: Whether you're training a new team or upskilling yourself, this bundle equips you with the latest, industry-standard knowledge and skills. Join a community of professionals committed to excellence in clinical research. 🔗 Enroll Now https://lnkd.in/dPS9aUuV #ClinicalResearch #CRA #ProfessionalDevelopment #Pharmaceuticals #Training #CareerAdvancement #EnrollNow 🎓🔬🌐

Ready for More than Just Individual Courses? Discover Our 'Learning Paths' Bundles! Each bundle is a carefully curated collection of top-tier courses designed to help you master specific regulatory topics: GMP, GLP, GDP, GCP, GVP, GxP, or Medical Devices. 🏆 Upon completion of each course, earn a unique and traceable certificate - a testament to your enhanced skills and knowledge in these critical areas, and ready to be shared on your LinkedIn profile. Our Learning Paths aren't just courses; they're your roadmap to becoming an authority in your field. Whether you're starting out or looking to deepen your expertise, these paths are structured to guide you through every detail of the topic. Start your Training Journey with our GxP Learning Path curated by the finest experts in the industry.👇🏼 https://lnkd.in/exrM_dX6 #certification #gxp #gmp #gcp #gdp #glp #onlinecourses