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An Introduction to Technology Transfer for Solid Dosage Forms Training Course

This course covers technology transfer for solid dosage forms, focusing on best practices, strategies, and real-world challenges through interactive sessions and case studies.

4 July 2025
+ 14 November 2025, 6 March 2026 »

from £649

Need help?  Enrol/reserve

Course overview

This course offers a foundational understanding of technology transfer specific to solid dosage forms, blending theoretical insights with practical applications. Through interactive sessions and case studies, participants will explore best practices for scale-up and technology transfer, strategise for smooth transitions, and master the critical do’s and don'ts of the process. Real-world examples will be analysed to highlight practical challenges and solutions, equipping learners with the tools needed for effective implementation in the pharmaceutical industry.

This course is part of our GxP training (Good x Practice) course collection, which features a variety of topic areas to ensure you comply with the most recent quality guidelines. For more information on the latest EU GMP regulations, see our GMP training course covering the Annex 1.

Benefits of attending

  • Gain practical knowledge from interactive sessions and case studies
  • Learn an outline of the proven best practices for scale-up and technology transfer
  • Discover how to strategise for a seamless technology transfer
  • Enhance your understanding of the do’s and don’ts during technology transfer
  • Analyse real-world examples to understand practical application and challenges

Who should attend?

  • Project managers
  • Tech transfer specialists
  • CMO managers
  • R&D process managers
  • Manufacturing project managers

Enrol/reserve

This course will cover:

Quality by design principles during process development and scale-up

  • Pharmaceutical QbD: why is it needed? What is it?
  • The importance of a good quality target product profile
  • How to best identify critical quality attributes, critical material attributes and critical process parameters
  • Examples of QbD for different formulations

Quality by design principles during process development and scale-up

  • Risk and science-based development: how to apply ICH Q9
  • Process control strategy: how to build an appropriate control strategy
  • Risks for solar dosage formulations: overview and examples
  • Case study in groups

Technology transfer challenges

  • When/why to perform a technology transfer
  • How to perform a technology transfer: ideal vs real life examples
  • Outsourcing and its challenges (also from a CMO perspective)

Planning for a seamless technology transfer

  • How to assemble a tech transfer team
  • Planning: activiteit and documentation
  • Example: best practices at sending and receiving site
  • The importance of engineering runs
  • Case study

Enrol/reserve

Laura Buttafoco
Protea

Laura’s areas of expertise include CMC strategy, technology transfer, process scale-up, validation, program management, GMP compliance and risk management. Laura has spent nearly 20 years in the industry where she has contributed to both small and large molecule projects. Acting as the main point of technical contact, as well as project/program manager, she has been responsible for completion of technology transfer and exhibit batches production in cooperation with various CMOs in EU, India and China. Currently she operates as independent consultant for Protea, her own company (www.protea.services). In this role, she has worked on a variety of therapeutics and she has a proven track record of successfully closed large Capex assignments on behalf of medium as well as large and well-established pharmaceutical companies.

More details

NEW higher discounts for multiple bookings - bring your colleagues to make your training budget go further:

  • 30% off the 2nd delegate*
  • 40% off the 3rd delegate*
  • 50% off the 4th delegate*

Please contact us for pricing if you are interested in booking 5 or more delegates

4 July 2025

Live online

09:00-16:30 UK (London) (UTC+01)
10:00-17:30 Paris (UTC+02)
04:00-11:30 New York (UTC-04)
Course code 15568

  • GBP 649 749
  • EUR 909 1,049
  • USD 1,043 1,199

Until 30 May

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Not ready to book yet?

for 7 days, no obligation

14 November 2025

Live online

09:00-16:30 UK (London) (UTC+00)
10:00-17:30 Paris (UTC+01)
04:00-11:30 New York (UTC-05)
Course code 15571

  • GBP 649 749
  • EUR 909 1,049
  • USD 1,043 1,199

Until 10 Oct

View basket 

 
Not ready to book yet?

for 7 days, no obligation

6 March 2026

Live online

09:00-16:30 UK (London) (UTC+00)
10:00-17:30 Paris (UTC+01)
04:00-11:30 New York (UTC-05)
Course code 15572

  • GBP 649 749
  • EUR 909 1,049
  • USD 1,043 1,199

Until 30 Jan

View basket 

 
Not ready to book yet?

for 7 days, no obligation

* Early booking discounts may not be combined with other discounts or offers. As such, the discounts for 2nd/3rd/4th delegates are based on the full price; and apply only when booking multiple delegates on the same date.

Run An Introduction to Technology Transfer for Solid Dosage Forms Live online for your team

1 day

Typical duration

Pricing from:

  • GBP 500
  • Per attendee, based on 10 attendees
  • Course tailored to your requirements
  • At your choice of location, or online

 

We can customise this course to your requirements and deliver it on an in-house basis for any number of your staff or colleagues.

Contact our in-house training experts Aleksandra Beer and Yesim Nurko to discuss your requirements:

Multiple colleagues? See above for details of our discounts for 2, 3, or 4 delegates. For more, talk to one of our training experts to discuss how to:

Run this course conveniently and cost-effectively in-house for your staff and colleagues

Aleksandra Beer

Aleksandra BEER
Training expert

Yesim Nurko

Yesim NURKO
Training expert

+44 (0)20 7749 4749

inhouse@ipi.academy