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  1. Home/
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  3. Process Scale-up, Validation & Technology Transfer
Process Scale-up, Validation & Technology Transfer
Scale up
Pharma & Biotech
CMC

Process Scale-up, Validation & Technology Transfer

15 – 17 June 2026

Price available after dates are announced

TRAINING TIMES

  • 09:00 - 13:30Vienna
  • 08:00 - 12:30London
  • 03:00 - 07:30New York
  • 00:00 - 04:30Los Angeles
Online Training



LEARNING OBJECTIVES

Learning Objective

Understand industry approaches for Scale-up, Technology Transfer, and PV applying QbD principles

Understand industry approaches for Scale-up, Technology Transfer, and PV applying QbD principles

Learning Objective

Gain regulatory insights & guidance on how to realize Technology Transfers and PV

Gain regulatory insights & guidance on how to realize Technology Transfers and PV

Learning Objective

Explore proven best practices in Scale-up for solid dose manufacturing processes

Explore proven best practices in Scale-up for solid dose manufacturing processes

Learning Objective

Gain practical knowledge and tools during two interactive sessions and workshops

Gain practical knowledge and tools during two interactive sessions and workshops

Learning Objective

Take an excellent opportunity to discuss issues & challenges with industry peers and with an expert

Take an excellent opportunity to discuss issues & challenges with industry peers and with an expert



KEY TOPICS

QbD Principles during Process Development and Scale-Up
Scale-Up of Granulation and Tableting Process
Technology Transfer: Regulatory, Planning & Execution
Process Validation new guidance and requirements
Process Design Stage: Key input for Product and Process Quality
Process Performance Qualification
Continued Process Verification
Process risk assessment

TRAINER

Dr. Michael Braun

Dr. Michael Braun

Boehringer Ingelheim Pharma, Director Late Stage Drug Product Development

Michael Braun, Ph.D., is currently Director of Late Oral Drug Product Development at Boehringer Ingelheim Pharma GmbH & Co KG in Biberach, Germany. Michael has a Ph.D in Pharmaceutical Technology from University of Bonn, Germany. His career is spanning over 25 years in pharmaceutical R&D, from hands-on formulation work to strategic leadership in drug development and manufacturing. Michael's journey began in 1999 as a Formulation Scientist at Ratiopharm and later as Head of Pharmaceutical Development at Rentschler Pharma in 2003. His career has evolved through various roles in early and late stage drug product development, clinical trial manufacturing and project management at Boehringer Ingelheim since 2006. Over the past two years Michael has worked at the Ridgefield Site, CT as the Director of Solid-State Sciences & API Engineering, driving innovation at the interface of drug substance and product development.

Learn More →

Sneak peek

Sneak Peek

Take a sneak peek at the trainer's presentation.

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