Compliance training panel, Online Webinar
2018-10-23
Description :
In this webinar we will discuss the regulatory expectations that apply to the production and control of active pharmaceutical ingredients. The discussion will start with the introduction of ICH Q7, the internationally accepted GMP for APIs, and discuss how this is supplemented by contemporary guidance such as ICH Q10, the Pharmaceutical Quality System, ICH Q8, Pharmaceutical Development, ICH Q9 Quality Risk Management and ICH Q11, Development and Manufacture of Drug Substances. The impact of new FDA guidance on Process Validation and Quality Metrics will also be considered.
Why you should attend :
The objective of this webinar is to provide a contemporary quality system approach to the production and control of active pharmaceutical ingredients. Although ICH 7, Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients is only 15 years old, the pharmaceutical industry has gone through a significant transition to a quality system approach to development, compliance, production, and control. Compliance activities that include these contemporary concepts must be practiced in a compliant organization.
Areas Covered in the Session :
The following areas will be included: - Drug GMPs
- ICH Q7
- ICH Q8
- ICH Q9
- ICH Q10
- ICH Q11
- FDA Process Validation guidance
- Data Integrity
- Quality Metrics
Who Will Benefit: 1. In the API manufacturer 1. Senior management 2. Site managers 3. Materials 4. Production 5. Quality Control 6. Quality Assurance 1. Reviewer 2. Auditor 2. In the Drug Product Manufacturer 1. Purchasing agents 2. Quality Assurance 3. Quality Control 4. Quality auditor
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