Navneet Sharma, PhD, is an Assistant Professor at Amity Institute of Pharmacy, Amity University, India.Vikesh Kumar Shukla, PhD, is an Associate Professor and Centre Head at Amity Institute of Pharmacy, Amity University, India.Sandeep Arora, PhD, is a Professor and Director at the Amity Institute of Pharmacy, Amity University, India.

• 1. US Pharma Manufacturing Standards: Cfr 210 & 2112. A Comprehensive Review on the Good Manufacturing Practices Standards: Directive 91/356 of the European Commission3. Integration Of Cgmp & Gamp-5 In Pharmaceutical Manufacturing4. Medical Device and Ivds Global Harmonization Task Force Guidance Documents5. Current Scenario and Future Perspective of Good Laboratory Practices6. Advancing Laboratory Excellence: A Comprehensive Review of Quality Audits7. Introduction of Good Automated Laboratory Practices (Galp): Principles and Comparative Analysis Across Regulatory Authorities - Usfda, Ema, Cdsco, And Tga8. A Framework to Understanding E-Records Under 21cfr Part 119. Current Trends in Good Distribution Practices (Gdp)10. Navigating The Pharmaceutical Supply Chain: Ensuring Integrity Amidst Challenges11. Optimizing Pharmaceutical Quality: Exploring Out of Specification, Total Quality Management, Change Control12. Insights Into the Six Sigma Concept13. Good Regulatory Practices and Validation Plans in Pharmaceutical Practices14. Critical Utility Validation: An Innovative Approach to Pharmaceutical Best Practices15. International Council of Harmonization: Reception to Implementation16. ISO-13485 and Schedule MIII – Quality Management System

Navneet Sharma, PhD, is an Assistant Professor at Amity Institute of Pharmacy, Amity University, India.Vikesh Kumar Shukla, PhD, is an Associate Professor and Centre Head at Amity Institute of Pharmacy, Amity University, India.Sandeep Arora, PhD, is a Professor and Director at the Amity Institute of Pharmacy, Amity University, India.

• 1. US Pharma Manufacturing Standards: Cfr 210 & 2112. A Comprehensive Review on the Good Manufacturing Practices Standards: Directive 91/356 of the European Commission3. Integration Of Cgmp & Gamp-5 In Pharmaceutical Manufacturing4. Medical Device and Ivds Global Harmonization Task Force Guidance Documents5. Current Scenario and Future Perspective of Good Laboratory Practices6. Advancing Laboratory Excellence: A Comprehensive Review of Quality Audits7. Introduction of Good Automated Laboratory Practices (Galp): Principles and Comparative Analysis Across Regulatory Authorities - Usfda, Ema, Cdsco, And Tga8. A Framework to Understanding E-Records Under 21cfr Part 119. Current Trends in Good Distribution Practices (Gdp)10. Navigating The Pharmaceutical Supply Chain: Ensuring Integrity Amidst Challenges11. Optimizing Pharmaceutical Quality: Exploring Out of Specification, Total Quality Management, Change Control12. Insights Into the Six Sigma Concept13. Good Regulatory Practices and Validation Plans in Pharmaceutical Practices14. Critical Utility Validation: An Innovative Approach to Pharmaceutical Best Practices15. International Council of Harmonization: Reception to Implementation16. ISO-13485 and Schedule MIII – Quality Management System