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Pharmig Academy

Sep 21, 2015 12:30 PM - Sep 23, 2015 4:30 PM

Garnisiongasse 4/4, 1090 Vienna, Austria

Quality by Design

QbD concepts are becoming defacto best practice spearheaded by the FDA and EMA. But how can you implement ICH Q8-Q11 with confidence for small molecules and biotech products?

Overview

Making Next Generation Process Efficiency a Reality for Chemical and Biotech Product Development and Optimisation

Quality by Design (QbD) concepts are becoming the defacto best practice spearheaded by the FDA and EMA. But how can you implement ICH Q8-Q11 with confidence for small molecules and biotech products?
As part of our Chemical Manufacturing series, DIA brings together expert faculty from Regulatory agencies, academia and industry. ICH and DoE expertise will accompany you to building a practical knowledge base.

METHODOLOGY & OUTCOMES
By the end of this 2.5-day course, you will have enough knowledge and reference points to establish a Design Space and essential elements of the Control Strategy. Through a series of  case studies you will learn how to use Quality Risk Management (QRM), Process Characterisation, Design of Experiments (DoE), Development of a Design Space and Control Strategy, as well as the tools of Knowledge Management (KM).

Case scenarios include:

  • solid dosage form of a small molecule
  • manufacturing process for a biotech product

You will learn how to prioritise the potential critical formulation and process parameters with QRM, propose, execute and evaluate a DoE to define the critical parameters and eliminate non-critical parameters.
Knowledge Management will be introduced to keep the information and knowledge gained transparent and available for the full lifecycle of the product. The case study will investigate how a systematic approach to pharmaceutical development and optimisation, respectively, will be faster and will lead to robust processes. Potential internal savings and regulatory flexibility will be discussed with a key European regulator.
The course will also provide an overview on global requirements including new relevant EU regulations and discuss opportunities for an optimal QbD submission.

What participants from previous courses say:
"Thank you very much for comprehensive overview of the subject and well-organized training course!"
"I am fully satisfied with this training course. The basic kowlegde about the QbD completed with the experimental works could support my work in any case. I liked very much the presentation about the tools for process characterisation as well"

What you will learn

  • Quality by Design for biotech products and small molecules
  • Prior Knowledge, Knowledge Management and QTPP Development
  • Initial Risk Assessment (FMEA), Introduction to Process Characterisation and Design of Experiments
  • Experimental Work, Multi-variate Data Analysis (MVA) and Knowledge Space Establishment
  • Design Space Definition
  • Control Strategy
  • Technologies Assisting QbD Approach
  • Regulatory Flexibility and QbD submission strategies
  • Post-Approval Change Management Protocol

Who should attend?

  • Pharmaceutical scientists, chemists, biologists and engineers
  • Experts from industry (pharmaceutical companies, biotech companies, generic industry)
  • Regulators with experience in pharmaceutical, chemical and biotech development, manufacturing, quality assurance and CMC

Learning objectives

At the conclusion of this course, participants will be able to:

  • Understand what QbD for biotech and small molecules is
  • Define how critical formulation and process parameters are identified
  • Use Quality Risk Management in the context of QbD
  • Use tools of scientific process characterisation
  • Plan and evaluate basic experimental designs for a QbD submission
  • Develop a Design Space
  • Develop a Control Strategy
  • Develop a Knowledge Management structure
  • Understand how to submit QbD data and get regulatory flexibility

This course is a hands-on course full of practical work. It is necessary that you bring your laptop with you.

Participants will complete a knowledge check at the end of the course and will be provided with feedback to ensure learning objectives are attained.

Digital Learning Catalog

DIA Learning: eLearning Soultions
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Ways to register

Registration fee includes refreshment breaks, lunches and training course material.

This course has limited capacity. Register early!

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