header-image

GMP meets Development - Live Online Training

6-8 November 2023

Seminar-Nr. 20639

Referent:innen

Dr. Joachim Ermer

Dr. Joachim Ermer

Ermer Quality Consulting

Dr. Sue Mann

Dr. Sue Mann

Sue Mann Consultancy

Katja Kotter

Katja Kotter

Vetter Pharma-Fertigung

Dr. Ulrich Kissel

Dr. Ulrich Kissel

European QP Association (EQPA), KisselPharmaConsulting

Note: All times mentioned are CET.

Zielsetzung

During this Live Online Training Course, specialists will share their expert knowledge about all important GMP aspects in Pharmaceutical Development and Investigational Medicinal Product (IMP) Manufacturing. You will be able to elaborate and discuss both EU and FDA requirements.

Hintergrund

Not only in the manufacturing of marketed products (c)GMP Compliance is mandatory. Also in the manufacturing of IMP supplies, compliance with the applicable GMP Guidelines is obligatory. But which GMP requirements are the applicable ones? And do the requirements differ from clinical phase 1 to phase 3? And what is the role of ICH Q8, Q9, Q10 and Q12?
 
With the third revision of ICH E6 (ICH E6(R3)), the GMP for IMP principles will be expanded to the following: Risk-based approaches should be considered when implementing proportionate measures to ensure GMP and the appropriate shipping and handling of the IMP.
 
Previously, the WHO already published two new draft documents relating to Development and GMP for IMPs: „Good Practices for Research and Development Facilities of Pharmaceutical Products“ and „GMP for IMPs“.
 
In addition, instead of the current EU GMP Annex 13 (Manufacture of IMPs), the Detailed Commission guidelines on GMP for IMPs for human use apply since 31 January 2022.
 
Complex challenges have to be faced and resolved to guarantee high quality products. The safety of the drug and hence also the patient should always be the main focus. Terminated studies or studies without reliable results will lead to extensive extra costs and delays in the whole development and approval process.
 
This Live Online Training has been designed by the ECA to broaden your knowledge and to consolidate the various GMP aspects which need to be considered in a successful development of a new pharmaceutical product.

Zielgruppe

This Live Online Training Course has been designed for R&D personnel involved in Pharmaceutical Development, IMP Manufacturing, Quality Control, Quality Assurance, and Regulatory Affairs.

Technical Requirements

For our webinars, we use Cisco WebEx, one of the leading suppliers of online meetings.
At http://www.webex.com/test-meeting.html you can check if your System meets the necessary requirements for the participation at a WebEx meeting and at the same time install the necessary plug-in. Please just enter your name and email address for the test. If the installation is not possible because of your rights for the computer system, please contact your IT department. WebEx is a Standard nowadays and the necessary installation is fast and easy.

Programm

GMP meets Development - Live Online Training

Gesamtes Programm als PDF herunterladen

6 November 2023
 
Global GMP Requirements from Phase 1 to Scale-up and Transfer
  • Global requirements: applicable law, directives, guides and guidelines: what is really required
  • A comparison of FDA and European requirements and expectations
The GMP/GDP/GCP Interface
  • Reconstitution
  • Pre-requisites for randomisation and blinding
  • Distribution
  • Site-to-site Transfers
  • Shelf life extension
  • The QP: where does the responsibility end?
IMP Manufacturing: How much Qualification and Validation is needed?
  • Qualification vs. Validation
  • What can be found in the regulations
  • DQ/IQ/OQ of equipment
  • How much process validation is needed?
Case study / Interactive session 1
Transition of GMP Requirements from Phase 1 to Phase 3 and the Interface to Development Work
  • Challenges and Differences
  • How to apply phase appropriate GMPs
  • Managing a GMP Lifecycle
Q&A Session 1
 
 
7 November 2023
 
IMPs in the Context of ICH Q8-Q10, Q12 and Q14
  • How to integrate Quality by Design
  • Risk Analysis in pharmaceutical development
  • Life cycle concept
Cleaning Validation / Verification in Pharmaceutical Development
  • Cleaning validation vs. cleaning verification
Change Control for IMPs
  • What is required
  • What is important
  • What are the benefits
  • How to implement
Analytical Development (ICH Q14)
  • From method development to method validation
  • How to deal with genotoxic and other impurities
  • Quality control and IMP release
  • Analytical Qualification
Q&A Session 2
 
Case study / Interactive session 2
Stability Studies throughout the Development of a new Product
  • Different types of products in CT studies (and support)
  • APIs and various dosage forms
  • Late stage stability strategies
The Role of the QP in Pharmaceutical Development and IMP Release
  • Responsibilities
  • Co-operation with Head of Production and Head of Quality Control
  • Confirmation of Compliance, certification and batch release
  • Comparators
  • Complaints and recalls
Q&A Session 3
 
 
8 November 2023
 
How to handle Deviations in an R&D Environment
  • Why we need a process for Deviations
  • What we need to know
  • How to do it
The FDA Pre-Approval Inspection (PAI)
  • Involvement of the R&D Department
  • What the FDA will look for
  • What happens at FDA during and after the PAI
  • Responding to FDA after the PAI
Important Documents in Pharmaceutical Development
  • Early documentation
  • CTD
  • PSF: style and Content
  • Case studies
Q&A Session 4

Case study / Interactive session 3
Data Integrity
  • Manufacturer‘s understanding of data integrity, needs and benefit
  • Regulatory expectations
  • Hybrid systems (paper and electronic records) - how to ensure data integrity?
Packaging and Supply of Clinical Trial Materials
  • GMP requirements
  • Quality control of packaging and labelling
  • Handling and sourcing of comparators
  • Randomisation and blinding
Q&A Session 5

Dieses Seminar/Webinar kann nicht gebucht werden. Alternative Termine für dieses Seminar/Webinar und ähnliche Veranstaltungen finden Sie in der Übersicht nach Thema..

Für viele Seminare und Webinare gibt es auch Aufzeichnungen, die Sie jederzeit bestellen und anschauen können. Diese Aufzeichnungen finden Sie in einer themensortierten Liste.

Oder senden Sie uns Ihre Anfrage einfach über das folgende Kontaktformular.

* auch unkompliziert per Kreditkarte bezahlbar
American Express Visa Mastercard

icon
Weitere Termine vor Ort
Weitere Termine vor Ort nicht verfügbar
icon
Weitere Termine online
Weitere Termine online nicht verfügbar
icon
Aufzeichnung nicht verfügbar

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

Frau mit Headset

Zurück

Teilnehmerstimmen - das sagen andere über unsere Seminare:

Guter, breit gefächerter Überblick mit interessanten Verknüpfungen zur Praxis,
welche die Theorie super veranschaulicht.”
Marina Kicoranovic, Labor Hartmann GmbH
GMP/Basis-Einstiegsschulung (B 14), September 2023

Die Referenten waren sehr gut! Sie haben sehr klar gesprochen, nur sehr wenige englische Begriffe
verwendet (super) und waren sehr praxisbezogen.”
Astrid Gießler, Regierungspräsidium Karlsruhe
Live Online Seminar - Basiskurs Computervalidierung & Datenintegrität im GxP Umfeld (B 3), Juni 2023

Sehr guter Bezug zur Schulung für einen GMP-Anfänger. Habe mich sehr gut abgeholt gefühlt.”
Dr. Harald Werner, Infraserv GmbH & Co. Höchst KG
GMP-Basisschulung (B 1), Juni 2023

NEWSLETTER

Bleiben Sie informiert mit dem GMP Newsletter von Concept Heidelberg!

GMP Newsletter

Concept Heidelberg bietet verschieden GMP Newsletter die Sie auf Ihren Bedarf hin zusammenstellen können.

Hier können Sie sich kostenfrei registrieren.

Kontakt

Kontaktieren Sie uns

Haben Sie Fragen?

Concept Heidelberg GmbH
Rischerstraße 8
69123 Heidelberg

Tel. :+49622184440
Fax : +49 6221 84 44 84
E-Mail: info@concept-heidelberg.de

zum Kontaktformular