Quality Reviews in the Context of FDA, EU and ICH Requirements and Expectations
- EU-GMP: which types of Quality Reviews are required?
- EU Quality System Review (overview)
- How to achieve EU-GMP compliance
- ICH/US-FDA view on the situation (overview)
- EU Product Quality Review (PQR)
- Technical terms and aims of PQR
- What documents and data should be reviewed?
- Are EU-requirements the same for APIs & medicinal products?
- What about US-FDA and ICH?
PQR and APR
- How to combine PQR and APR in an efficient way
- Well-proven PQR/APR designs
- Interface to Regulatory Affairs
- Certainties (PQR/APR in Custom Manufacturing, how to deal with limited numbers of batches …)
EU Product Quality Reviews in the Light of Inspections – Expectations of the Agencies
- Inspectors view on critical parts of EU-PQR
- Practical implementation and inspection
- PQR and contract manufacturing
- Comparison EU-PQR and US-APQR (inspectors point of view)
Discussion of given PQR-Examples
Based on real examples, the speaker will discuss the content and lay-out of PQRs:
- What is useful?
- What is ambiguous?
- What could be improved?
Set up of efficient PQRs and APRs
- How to profit from existing QA Systems in PQR/APR and vice versa
- Best practices
- Time/efforts needed
- Ongoing data collection
- Foreseeable complications/advantages
- Well-proven examples
Management Review
- Definition, scope, objectives
- Organisation
- Participants, responsibilities
- Topics to be presented: input and output
- KPIs per system
- Examples and experience
Using KPI in Quality Reviews and in Communication with Authorities
- Current status of the requirements
- Key areas and data to be submitted
- How industry can prepare to meet the expectations
Quality Reviews in Contract Manufacturing
- Customer QMRs - content, scope, frequency, organisation
- Interface with Business Management Reviews
- Assessment of data, trending and decision making
- Actions, follow-up
- „Face to Face“ or telecon?
Kite Pharma Case Study: Management Review - from Data Collection to Evaluation and Reporting
- Collection and preparation of data: time/efforts needed, automatic vs. manual data capture
- Evaluation of deviations and changes
- Interpretation of data: what is the data telling us?
- How to report the data and information gained
Review Management: Bringing them all together in an efficient Way
- How to set up an integrated data, review and Report management
- How to avoid double work
Question and Answer Sessions
A set of live Q&A Sessions will give you the possibility to interact with the speakers and get answers to your questions.
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Pre-Course Session:
Quality Reviews in the Context of FDA, EU and ICH Requirements and Expectations
- EU-GMP: which types of Quality Reviews are required?
- EU Quality System Review (overview)
- How to achieve EU-GMP compliance
- ICH/US-FDA view on the situation (overview)
- EU Product Quality Review (PQR)
- Technical terms and aims of PQR
- What documents and data should be reviewed?
- Are EU-requirements the same for APIs & medicinal products?
- What about US-FDA and ICH?
PQR and APR
- How to combine PQR and APR in an efficient way
- Well-proven PQR/APR designs
- Interface to Regulatory Affairs
- Certainties (PQR/APR in Custom Manufacturing, how to deal with limited numbers of batches …)
EU Product Quality Reviews in the Light of Inspections – Expectations of the Agencies
- Inspectors view on critical parts of EU-PQR
- Practical implementation and inspection
- PQR and contract manufacturing
- Comparison EU-PQR and US-APQR (inspectors point of view)
Discussion of given PQR-Examples
Based on real examples, the speaker will discuss the content and lay-out of PQRs:
- What is useful?
- What is ambiguous?
- What could be improved?
Set up of efficient PQRs and APRs
- How to profit from existing QA Systems in PQR/APR and vice versa
- Best practices
- Time/efforts needed
- Ongoing data collection
- Foreseeable complications/advantages
- Well-proven examples
Management Review
- Definition, scope, objectives
- Organisation
- Participants, responsibilities
- Topics to be presented: input and output
- KPIs per system
- Examples and experience
Using KPI in Quality Reviews and in Communication with Authorities
- Current status of the requirements
- Key areas and data to be submitted
- How industry can prepare to meet the expectations
Quality Reviews in Contract Manufacturing
- Customer QMRs - content, scope, frequency, organisation
- Interface with Business Management Reviews
- Assessment of data, trending and decision making
- Actions, follow-up
- „Face to Face“ or telecon?
Kite Pharma Case Study: Management Review - from Data Collection to Evaluation and Reporting
- Collection and preparation of data: time/efforts needed, automatic vs. manual data capture
- Evaluation of deviations and changes
- Interpretation of data: what is the data telling us?
- How to report the data and information gained
Review Management: Bringing them all together in an efficient Way
- How to set up an integrated data, review and Report management
- How to avoid double work
Question and Answer Sessions
A set of live Q&A Sessions will give you the possibility to interact with the speakers and get answers to your questions.