Analytical method Quality Auditing
Quality assurance (QA) and independent audit is critical in the pharmaceutical industry to assure reliability of the products, adherence to approved specifications, and conformation of current good manufacturing practices (cGMP) to regulation. Manufacturers must establish a quality control unit that is responsible for quality-related activities required by the regulations. Quality is determined by whether the firm complies with GMP requirements and makes scientifically justified decisions. Pharmaceutical companies are now taking a proactive stance with the new GMP Systems approach, more effective internal auditing and increased regulatory awareness throughout the company.
- Pharmaceutical Manufacturing Environment
- Quality Control
- Analytical Instruments
- Quality Management System (QMS)
- Quality Management System (QMS)
- Laboratory Control System
Related Conference of Analytical method Quality Auditing
Analytical method Quality Auditing Conference Speakers
Recommended Sessions
- Analytical method Quality Auditing
- Audit Planning to Ensure Maximum Effectiveness and Efficiency
- Auditing Deviations, Product Complaints, and CAPA Systems
- Clinical and Bioanalytical laboratory Audits
- Clinical Audit in Pharmaceutical Development
- GMP in Food Industry
- Goals and Strategies to Meet Audit Requirements
- Importance of Audit in Pharmaceutical Industry
- Pharmaceutical Auditing for OTC Drugs
- Quality Assurance Audits in Pharma Industries
- Quality Assurance, Quality Control and Audit
- Quality Management System in Testing Laboratories
- Regulatory Affairs