GMP and Schedule M Audit Service for Pharmaceutical Facilities
All pharmaceutical manufacturing facilities in India are required to comply with the Schedule M guidelines. The guidelines are intended to change the way pharmaceuticals are manufactured in India bringing them at par with global standards. However, ensuring compliance...
Effective Risk-Based CAPA in Quality Management System
Corrective Action Preventive Action (CAPA) focuses on eliminating the root cause of non-conformities It is a systematic approach aimed at mitigating the risks of undesirable events and non-conformities. CAPA forms the core of quality management system (QMS) in...
5 Key Changes in Revised Schedule M: A Comprehensive Guide
Significant changes in Revised Schedule M guidelines have been introduced to safeguard patients and improve the Indian pharmaceutical industry’s reputation. These new guidelines are aimed at changing the way pharmaceuticals are manufactured in India. For further...
Securing CDSCO Wet Wipe Manufacturing License in India
Wet wipes are moistened pieces of paper or non-woven fabrics that are used to clean surfaces. These premoistened wipes are usually available in small packs and are disposable. They are used to gently cleanse the skin. Additionally, they are used to remove impurities...