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Quality & Regulatory Requirements for Inhalation Drug Products

  • 22 – 24 May 2024
  • Online Live Stream | 13:00 CEST – 18:00 CEST | 12:00 UK Time – 17:00 UK Time
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Quality & Regulatory Requirements for Inhalation Drug Products

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Training features

Fully online

All sessions of this unique course online

Live interaction

Live interaction options between the delegates and trainer

On any device

Available via mobile, tablet or laptop

Course description

This course will cover the aspects of the human respiratory tract that are relevant to the delivery of medicines to the lungs. The course will cover Industry best practice to develop Metered Dose Inhaler (MDI) and Dry Powder Inhaler (DPI) products, the science and technology involved as well as aspects of safety, efficacy, quality, testing and stability testing for product & process understanding and generating data for regulatory product authorisations.

meet the training leaders
Tarlochan Singh Purewal | Speaker | Fleming
Linkedin
Tarlochan Singh Purewal, B.Sc. Pharmacy, PhD, MBA
Director
TSP Pharma Consulting Ltd, UK
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David Howlett | Speaker | Fleming
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David Howlett
Founder, Director
PharmaDelivery Solutions Ltd, UK
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Gerallt Williams | Speaker | Fleming
Dr Gerallt Williams
Director Scientific Affairs
Aptar Pharma, UK
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Brochure

Reveal the full schedule of the training as well as key topics, course objectives, key takeaways, special features, and the trainer bio!

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Quality & Regulatory Requirements for Inhalation Drug Products online live training organized by Fleming_Agenda Cover
Quality & Regulatory Requirements for Inhalation Drug Products online live training organized by Fleming_Agenda Cover
Quality & Regulatory Requirements for Inhalation Drug Products online live training organized by Fleming_Agenda Cover
key training

Topics

Formulation and development of pressurised Metered Dose Inhalers (MDI)

Methods of MDI manufacture & in-process quality control

Testing of Metered Dose Inhalers

Dry Powder Inhaler (DPI) Technology

Dry Powder Inhaler (DPI) Formulation

Dry Powder Inhaler (DPI) Regulatory Requirements

Dry Powder Inhaler (DPI) Manufacture

Dry Powder Inhaler (DPI) Testing

Key takeaways

  • Understand how to develop MDI & DPI medicinal products
  • Gain tips on how to keep development timelines as short as possible
  • Master design control for inhalation combination products
  • Discuss the challenges of developing, commercializing and registering inhalation products in the 2020’s
  • Get insights into current and evolving regulatory expectations for inhalation products
  • Best practices for testing product performance for both development and routine QC and product understanding
  • Explore how concepts such as, product design space, usability and risk management apply to inhalation products
Registration

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Contact us

Andrea Weber | Marketing Manager | Fleming
Linkedin
Andrea Weber
Sr. Manager for Pharma
Phone: +421 257 272 100
Email: event.inquiries@fleming.events

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