Excipient Qualification and Supply Chain Controls
Excipients play an important role in formulating a dosage form. These are the ingredients which along with Active Pharmaceutical Ingredients make up the dosage forms. Excipients act as protective agents, bulking agents and can also be used to improve bioavailability of drugs in some instances, Excipients affect the physicochemical characters of the active pharmaceutical ingredient which may lead to formation of molecular complexes, increase in rate of chemical degradation etc.
- Excipient Specifications and Stability
- Excipient Consistency and Control
- Excipient Risk Assessment
- Supply Chain Issues
Related Conference of Excipient Qualification and Supply Chain Controls
Excipient Qualification and Supply Chain Controls Conference Speakers
Recommended Sessions
- Auditing Deviations, Product Complaints, and CAPA Systems
- Excipient Qualification and Supply Chain Controls
- Importance of Audit in Pharmaceutical Industry
- Quality Management System in Testing Laboratories
- Analytical method Quality Auditing
- Clinical and Bioanalytical laboratory Audits
- Clinical Audit in Pharmaceutical Development
- Contract & Sterile/Aseptic Manufacturing
- Current GMP Guidelines (cGMP) & GxP in Pharmaceuticals
- Current Regulations and Quality Standards
- Formulation Development
- GMP in Food Industry
- GMP in Microbiology and Biotechnology
- Goals and Strategies to Meet Audit Requirements
- Good Clinical Practices & Good Laboratory Practices
- Good Manufacturing Practices: The Gap within
- Pharmaceutical Auditing for OTC Drugs
- Quality Assurance
- Quality Assurance Audits in Pharma Industries
- Quality Assurance, Quality Control and Audit
- Quality Control
- Softwares in GMP and GCP
- Storage, Distribution, Transportation
- The Role of c in cGMP
- Validation