Edicent Quality Registrar Private Limited EQR

15/08/2025

14/08/2025

DPMO Vs Sigma Score

12/08/2025

📢 Today’s EQR training session is ongoing at a reputed 🌐 MNC, focusing on enhancing 🏭 production, 🎨 designing, ✅ quality, and 📦 supply chain processes in line with 🌍 international standards.
💡 In a global culture of business, 🌱 sustainability and 🏆 business excellence go hand in hand—requiring not just 📜 compliance, but effective ⚙️ implementation and thorough 🗂️ documentation.
🚀 By strengthening systems across all levels, we aim to create a robust foundation for 📈 continuous improvement, ensuring our partner stays ahead in 🔝 performance, quality, and global competitiveness.

09/08/2025

📢 Awareness Training on ISO 17258:2015 🌍
📚 Covering all clauses, from the Introduction to detailed applications, this video is your complete guide to the Benchmarking Standard for quality, performance, and productivity improvement.

🔍 What You’ll Learn:
✨ Benchmarking Basics – Method, levels of comparison, quality & performance measurement, state-of-the-art approaches, improvement programs, quantifying progress 📊
📏 Evaluation Metrics – Regulatory compliance ✅, financial performance 💰, reference points 📌, transparency 🔎, and universal principles 🌐
🔄 Benchmark & Six Sigma Principles – Sigma measure 📉, 0–10+ scale, world-class standard 🌟 (3.4 DPMO), excellence in products & services 🏆, applicability to all sectors 🏭, and the link with DMAIC & DFSS 🔧
⚙️ Criteria & Defects – Understanding measurement standards & error reduction 🛠️
🚚 Supply Chain Benchmarking – From raw material to final product/service 📦, quality totals, competitive benchmarking 💪, and chain efficiency optimization 📈
📜 Methodology – Establishment process, levels of quality, performance & productivity, good benchmarking practices 📖
📚 Normative Reference – ISO 13053-1: Quantitative methods in process improvement – Six Sigma – Part 1: DMAIC methodology 📑
🧾 Terms & Definitions – Benchmarking method (logical sequence, quantitative attributes, specified scale) 📏
🔤 Symbols & Abbreviations – For quick reference and clarity 📝

💡 Perfect for:
✔️ Quality Managers 🧑‍💼
✔️ Process Improvement Teams ⚡
✔️ Supply Chain Professionals 🚛
✔️ Continuous Improvement Leaders 📈

📺 Watch now and take your organization’s performance to the next level of excellence! 🚀

Edicent Quality Registrar (EQR)Services: Certification, Training and Advising Contact Details: +91-8802650960; info@edicentcertification.org📢 Awareness Trai...

01/08/2025

ISO 17258:2015 Awareness Training Coming Soon!!

"📊 Six Sigma isn’t just about reducing defects — it’s about knowing where you stand. ISO 17258 helps you benchmark better. 💡"

"🚀 Performance. 📈 Progress. 🧠 Insight. ISO 17258:2015 shows how Six Sigma benchmarking truly works."

"Want to compare your Six Sigma success with the best? 🌟 ISO 17258 gives you the framework.

"🔍 Understand. 📏 Measure. 🎯 Improve. ISO 17258:2015 turns Six Sigma benchmarking into a strategic tool."

29/07/2025

📌 AIAG CQI-8 Layered Process Audit (LPA) – Full Awareness Training | All Clauses & Introduction Covered!
🔍 Dive deep into the Layered Process Audit (LPA) as defined in AIAG CQI-8, through this awareness training that covers all clauses and the full introduction – perfect for professionals looking to enhance process control, compliance, and communication.

🧠 What You'll Learn in This Video:
✅ LPA Definition & Purpose: A robust management tool used to verify conformance to established standards across any defined process for product or service creation
✅ LPA Value: Improved performance metrics, reduced quality incidents, first-hand feedback, and minimized cost of poor quality (COPQ)
✅ Boost two-way communication, drive shared ownership, and enhance more verification than control

🛠️ Roles & Responsibilities:
👤 LPA Process Owner (PO): Oversees results, corrective actions, new process facilitation, documentation & communication
🧑‍💼 Operations & Area Managers: Plan, conduct, and review LPAs with resource availability and corrective action implementation
🤝 LPA Planning Team: Cross-functional team from across departments, guided by PO, defines scope and audit criteria

📋 Core Topics Covered:
📌 LPA Scope: Identification of critical process characteristics, relation to internal/third-party MSA, fully documented and approved processes
📈 Process Prioritization: LPA-first approach, review by severity, frequency & performance
📊 LPA Metrics: Development of meaningful indicators to measure LPA effectiveness
🗂️ Templates & Reporting: Standardized, controlled formats for checklists, corrective actions, and follow-ups
👥 Audit Layers: Engagement from multiple levels, including corporate executives, promoting visibility and communication
🤝 Stakeholder Buy-in: Achieving cross-departmental support through planning, communication, and structured ex*****on

🎓 Why Watch?
Get a complete awareness training on LPA

All clauses and the introduction of CQI-8 are clearly explained

Improve audit performance, KPI alignment, and business results

Align your LPA process with ISO 9001, IATF 16949, and customer-specific requirements

👉 Ideal for: Quality Professionals, Process Engineers, Auditors, and Operations Managers seeking a structured and effective LPA program.

🔔 Don’t forget to like, share, and subscribe for more training content on automotive standards, quality tools, and process improvement!

🚗📘✅

Edicent Quality Registrar (EQR)Services: Certification, Training and Advising Contact Details: +91-8802650960; info@edicentcertification.org📌 AIAG CQI-8 Lay...

27/07/2025

🔍 Coming Soon: Master the Art of Layered Process Audits (LPA)! 🎯
Based on AIAG CQI-8, our upcoming training video will help you understand and implement LPA as a powerful quality management tool to ensure process compliance, drive continuous improvement, and boost operational discipline 🚀
✅ Improve accountability
✅ Enhance process standardization
✅ Detect issues before they become defects
✅ Build a culture of quality
Whether you're in automotive manufacturing or general operations excellence, this is your chance to elevate your systems to world-class standards! 🌍
🎥 Stay tuned. Hit the 🔔 notify button and don’t miss out!
🎓🛠️📊

https://www.youtube.com/-Quality

26/07/2025

"On this 26th July, we salute the bravery, honor the sacrifice, and remember the heroes who proved that for them, the nation was above all. Kargil Vijay Diwas — an eternal inspiration."

24/07/2025

🔷 Awareness Training on Standard Requirements for Medical Device QMS (MDQMS) | All Clauses Covered 🔷
Welcome to our comprehensive Awareness Training Session, where we break down all standard clause requirements essential for building, implementing, and maintaining an effective Medical Device Quality Management System (MDQMS). This training is tailored to guide organizations—regardless of their size, type, or complexity—through the key concepts, processes, and regulatory expectations in line with international standards.
💡 What This Training Covers:
✅ Introduction & General Requirements
Understanding the complete product lifecycle
Role of interrelated organizations (excluding voluntary external parties
Identifying regulatory and technical requirements
Strategic importance and influence of MDQMS
Need for uniformity and structured implementation
✅ Clarification of Key Concepts
ons of "appropriate", "risk", "documentation", "product & service"
Regulatory requirements and proper verbal forms:
✅ Process Approach
Input ➝ Output ➝ Input loop
Linked processes, value addition, performance, and effectiveness monitoring
Process improvement and continuous compliance
✅ Relationship with ISO 9001
Alignment with general QMS regulatory requirements
Addressing particular needs for the medical device industry
✅ Compatibility with Other Management Systems
Integration with broader QMS
Limitations and system coherence
✅ Demonstrating Compliance
Meeting both customer and regulatory expectations
Applicability across all organization types and sizes
Vendor responsibility and design & development exclusions
✅ Normative References & Definitions
Role of ISO 9000
Key terms: advisory notice, authorized representative, clinical evaluation, importer, distributor, implantable medical device, and more
✅ General & Documentation Requirements
Documenting QMS, processes, responsibilities, procedures
Managing outsourced processes, risks, and software validation
Structure and contents of the Quality Manual
✅ Medical Device File
Requirements per device: specs, measurements, installation & servicing procedures
✅ Control of Documents & Records
Approval, updates, accessibility, legibility
Management of external and obsolete documents
Record confidentiality, traceability, and retention
📚 Whether you're new to medical device quality systems or seeking to deepen your understanding, this training provides a structured, clause-by-clause awareness necessary for compliance and excellence.
👉 Don’t forget to Like, Share & Subscribe for more training content on ISO standards and regulatory systems.



📩 For training, certification, and advisory services, contact us:
📧 info@edicentcertification.org
📞 088026 50960

Edicent Quality Registrar (EQR)Services: Certification, Training and Advising Contact Details: +91-8802650960; info@edicentcertification.org🔷 Awareness Trai...

20/07/2025

Internal Audit
Get an inside look at our Internal Audit process, a crucial step in maintaining our ISO 14001:2015 certification for our Environmental Management System (EMS)! 🌎💼 This audit ensures we're meeting the highest standards for environmental responsibility and sustainability. Check out our latest video to learn more about our commitment to reducing our ecological footprint:

Edicent Quality Registrar (EQR)Services: Certification, Training and Advising Contact Details: +91-8802650960; info@edicentcertification.orgWith the help of ...

20/07/2025

Performance Evaluation
Elevate your organization's environmental management system with our latest Performance Evaluation video, now available! 📹️ This in-depth session provides a comprehensive overview of and EMSTraining, offering actionable insights, practical expertise, and strategic guidance to enhance your organization's performance and ensure a sustainable future. 💡️ You'll gain a deeper understanding of how to identify areas for improvement, set meaningful targets, and develop effective strategies to minimize your environmental footprint. Additionally, discover the benefits of integrating environmental considerations into your business operations, including cost savings, improved brand reputation, and increased stakeholder trust. Watch now to optimize your environmental performance, mitigate risks, and capitalize on opportunities:

Edicent Quality Registrar (EQR)Services: Certification, Training and Advising Contact Details: +91-8802650960; info@edicentcertification.orgWith the help of ...

19/07/2025

Watch full video at our YouTube official channel 🔴 ISO 45001:2018 Full Training | Complete Clause-wise Explanation (Clause 1 to 10)

Welcome to Edicent Quality Registrar's official training video on ISO 45001:2018 – Occupational Health & Safety Management System (OH&SMS).

This comprehensive video covers the entire structure of the standard, including:

✅ Introduction to ISO 45001
✅ Clause 1 to Clause 10 – Detailed Explanation
✅ Practical insights for implementation
✅ Alignment with legal and organizational compliance

Whether you're a professional, auditor, safety officer, or management system learner, this video is designed to:

🔹 Enhance your understanding of OH&SMS
🔹 Support your preparation for the Lead Auditor Examination
🔹 Improve your competency and implementation skills
🔹 Strengthen your company’s safety culture and compliance practices

🎯 After watching this video, you will have a clear grasp of how ISO 45001:2018 works, how to interpret each clause, and how to apply it effectively in your organization.

👉 Don’t forget to Like, Subscribe, and Share to support more such quality learning content.

📩 For training, certification, and advisory services, contact us:
📧 info@edicentcertification.org
📞 +91-8802650960
🌐 www.edicentcertification.org