Quality Assurance
- Quality Assurance is responsible for the site compliance, realization, and specific maintenance further development of internal Quality Management Systems. Quality Assurance ensures that APIs and Intermediates produced from various stages of manufacturing comply with CGMP requirements. Following are a few of the important activities handled by the Quality Assurance team.
- Document control & Annual Product reviews
- Monitoring of all validations including cleaning validations
- Change control compliance, batch release & product recall
- GMP training & awareness
- Vemed Pharmaceuticals aims at achieving a high degree of quality in our products and services through investing in modern technologies and upgrading manufacturing facilities from time to time. Our vision is to achieve international standards of quality, through persistent hard work and better implementation of knowledge by the people and having a quality policy in place. Our quality systems are designed as per ICHQ Guidelines and to implement these standards. We have a thorough training and re-training program in place.
- The quality department at Vemed is well equipped with various instruments, stability chambers, retain samples, etc., for all necessary testing and studies.
