Zielsetzung
The EU GMP Conference is only offered every two years. This unique conference will discuss current and planned changes to the GMP regulation. All experts and managers involved in GMP compliance activities will have the opportunity to get a comprehensive GMP update and to talk to the leading experts from industry and authority
Although EU GMP is in the center of attention, a harmonized approach with cGMP from FDA will also be an important aspect of the agenda. For international operating companies both EU GMP and FDA compliance is important and the corporate quality systems need to cover the regulation of both regions.
The agenda will therefore focus on key GMP compliance developments. Attention will be paid on the implementation of these requirements into pharmaceutical quality systems. The ECA Foundation’s objective is to support industry, and therefore current activities as well as guidance documents and SOPs are presented during this conference.
Each Session will have speakers from industry and inspectorates to discuss both expectations and implementation aspects.
We wish you a successful and interesting conference.
Yours sincerely,
Richard M. Bonner
Chairman of the ECA Advisory Board
Zielgruppe
The conference is of particular interest for GMP experts of pharmaceutical companies (e.g. QA, QC, production, distribution, regulatory affairs), of GMP inspectorates and Regulatory Authorities.
Special bonus for each particpant:
Each participant will receive a set of documents developed by the ECA working and interest groups such as:
Latest version of the GMP Matrix (comparison of EU GMP, FDA cGMP and ISO 9001)
OOS SOP developed by the Analytical QC Group
Validation Good Practice Guide developed by the Validation Group
Current chapters of the GDP interpretation developed by the GDP Group in cooperation with PQG
Programm
Gesamtes Programm als PDF herunterladen
This session will discuss the latest changes and current initiatives in EU GMP and FDA GMP regulation
Update from recent EU GMP changes
Latest Changes in EU Regulations
Latest Revisions of the EU GMP Guide and its Annexes
New EMA Guidelines with impact to GMPs
Look over the pond - Important GMP developments in the US
Dr Bernd Renger
FDA´s focus on Data Integrity
What are the reasons behind the new inspection focal point?
Data integrity concerns in the US, India and Europe – are there any differences?
The culture of error – how to avoid data integrity problems
Dr Ajaz Hussain
Formalized Risk Assessment for Excipients – a new task for every pharmaceutical company
What does a QP require of an excipient manufacturer?
Do excipients pose a risk to GMP? What could go wrong?
Are there ways to assess and mitigate the risks?
Is a Technical Agreement and Supplier Audit required?
What are the acceptable standards to apply to excipient manufacturers
Richard Bonner
Trending of GMP data is under discussion in the pharmaceutical industry and in authorities. What kind of data should be used for trending? What is a trend in a set of data? What are the consequences of a trend? This will be discussed in presentations covering trends in production and analytical data.
Trending from the regulators point of view
Trending requirements
Authorities’ expectations
Inspection findings
Dr Franz Schönfeld
Case Study: Trending in production
SPC as trending tool
Case Study
Dr Ingolf Stückrath
The new Out of Trend Guidance developed by the ECA Foundation Analytical QC Working Group
Regulatory need for trending analysis
Overview of Analytical QC Working Group
Generation process of this guidance document
Structure and content
Current status and next steps
Dr Chris Burgess
The new EU GDP Guide will not only have a huge impact on Logistic Service providers but will also require from pharmaceutical Industry to establish a system to control and monitor the distribution supply chain of it´s medicinal products.
The enhanced GMP and GDP Inspection activities from the point of view of an EU GMP/GDP Inspector
Authorities requirements
What changed with the EU GDP Guideline revision?
Inspection findings
EU Inspector, to be named
New GDP Guidance Documents and their implementation
Implementation of the EU GDP Guide for medicinal products
The new GDP Guide for APIs
Track and Trace – what will come next?
Dr Afshin Hosseiny
The new PQG/ECA Guidance Documents on GDP implementation
Current status of the documents
Lessons learned from interpretation
Next steps
Dr Afshin Hosseiny
This session will highlight the recent draft Annex 15 to the EU GMP Guide and the relating EMA and FDA Guidance documents.
The new EU GMP Annex 15 from the point of view of an EU GMP inspector
History of validation guidelines in the EU
The EU GMP Annex 15 revision
Links to EMA Process Validation Guideline
What´s really new?
Klaus Eichmüller
Process validation regulations at a crossroad: What should you do tomorrow?
Comparing FDA Process Validation Guidance and EU Annex 15
Equipment qualification: EU and US approaches
Continued Process Verification challenge and opportunities
Continuous manufacturing today and in the future
Gert Moelgaard
Get involved in the ECA Working Groups. Each delegate will be invited to discuss the upcoming developments with the Chair/Co-Chairs of the working groups.
Agenda
You can address topics of interest for you and you can provide feedback on the currently planned activities. It is the aim of the Working Group to provide a platform of discussion with both colleagues from industry and regulatory authorithies.
Social Event at the Heidelberg Castle
On 09 June, participants and speakers are cordially invited to a social event at the Heidelberg Castle. We will have a guided tour of the Castle followed by a dinner at the Castle Restaurant. This is an excellent opportunity to share your experiences with colleagues from other companies in a relaxed atmosphere.
Dieses Seminar/Webinar kann nicht gebucht werden. Alternative Termine für dieses Seminar/Webinar und ähnliche Veranstaltungen finden Sie in der Liste aller Seminare.
Für viele Seminare und Webinare gibt es auch Aufzeichnungen, die Sie jederzeit bestellen und anschauen können. Diese Aufzeichnungen finden Sie in der Liste aller Aufzeichnungen.
Oder senden Sie uns Ihre Anfrage einfach über das folgende Kontaktformular.
Haben Sie noch Fragen?
Wir stehen Ihnen für weitere Auskünfte gerne zur Verfügung.
Tel.: +49 6221 84 44 0
E-Mail: info@concept-heidelberg.de
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