Improve your Quality Reviews & pre-course session Statistical Process Evaluation and Reporting
Im Auftrag der ECA Academy

Improve your Quality Reviews & pre-course session Statistical Process Evaluation and Reporting Im Auftrag der ECA Academy

Barcelona, Spain

Seminar Nr. 17299


Kosten

Non ECA Member: EUR 2290,--
ECA-Member: EUR 1990,--
EU/GMP Inspectorates: EUR 1145,--
APIC Member Discount: EUR 2190,--
QP Member Discount: EUR 1990,--

Alle Preise zzgl. MwSt.

Rückfragen unter:
Tel.: 06221 / 84 44 0 E-Mail: info@concept-heidelberg.de

Sprecher

Dr Rainer Gnibl, GMP Inspector for EMA
Prof Edwin van den Heuvel, University of Technology Eindhoven
Dr Andreas König, Fidelio Healthcare
Dr Jens-Uwe Rengers, Consultant
Pia Lise Sandau, Novo Nordisk

Zielsetzung

This course examines regulatory requirements, provides insight into inspectors’ expectations and explains tools for improving your documented review processes.

Based on real examples you will learn how you can implement and improve your Quality Reviews and use them more efficiently.

Hintergrund

Quality Reviews and Metrics are critical GMP elements. They are an integral part of a pharmaceutical quality system and provide an opportunity to assess and control relevant processes.

Both parts of the EU-GMP Guidelines require the Product Quality Review (PQR) to verify the consistency and appropriateness of existing processes,  but also to identify product and process improvement opportunities.

The FDA 21CFR 211 requires an Annual Product Review (APR) to evaluate annually the quality standards of each drug product.

All relevant guidance do also consider a Management Review to be an appropriate instrument to assess adequacy and effectiveness of quality systems.
All these different reviews could result in a tremendous work load or they can be performed in an efficient way with useful results – depending on how they are organised. Therefore it is very important to understand the requirements and the idea behind it and to see how these tools can be used more efficiently.

Zielgruppe

This Education Course is designed for managers, supervisors and all other staff members in the pharmaceutical and API industry who are involved in preparing and compiling Quality Reviews and Metrics.

Every participant will get:

  • an example for  PQR SOP Annexes
  • an example for a Management Review SOP
  • real PQR examples
  • extracts from real Management Reviews

Programm

Pre-course Session Statistical Process Evaluation and Reporting
This pre-course session will provide you with recommendations, tools and examples to apply statistical principles in your day-to-day business and it will help you to meet future challenges.

You will gain understanding of the consequences of appropriate and inappropriate performance parameters and a sound evaluation of data also by working with statistical simulation tools.

The Application of statistical Tools in Data Review
  •  Introduction
    •  Ongoing/data collection and management
    •  Interpretation, comparison and presentation of  data
    •  Describing process capability and performance
    •  Control Charts; what is a trend and how to deal with it?
    •  Quality Metrics
    •  Documenting the outcomes; are we in control?
  •  Quality Review Summary Report
    •  Descriptive statistics
    •  Outlier detection
    •  Normality testing
  •  Quality Review Performance
    •  Control Charts
    •  Capability indices
The Session includes a Workshop with a statistical software to explain and understand: What are the Data telling us?

A case study on analysing and interpreting process performance data.

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?
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)
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 …)
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
Workshop: Evaluation of given PQR-Examples
Evaluate with other delegates the content and lay-out of given PQR-examples and discuss it with the speakers:
  •  What is useful?
  •  What is ambiguous?
  •  What could be improved?
Management Review
  •  Definition, scope, objectives
  •  Organisation
  •  Participants, responsibilities
  •  Topics to be presented: input and output
  •  KPIs per system
  •  Examples and experience
Novo Nordisk 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
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?
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
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

Zurück

GMP Seminare nach Thema

Cookies helfen uns bei der Bereitstellung unserer Dienste. Durch die Nutzung unserer Dienste erklären Sie sich damit einverstanden, dass wir Cookies setzen. Weitere Informationen

OK