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Mastering Pharmaceutical Rheology From Formulation Development to Scale-Up and Quality Control

Formation de base

As pharmaceutical products move from formulation development to commercial manufacturing, maintaining product performance, processability, and quality becomes increasingly critical. Rheology helps scientists and production teams understand how materials behave under real-world processing conditions, supporting better decisions throughout development, scale-up, technology transfer, and manufacturing.

Join us for this technical seminar to explore how rheological characterization supports pharmaceutical workflows from early formulation development through commercial production. Through practical examples, attendees will learn how rheology helps reduce scale-up risk, improve communication between R&D, manufacturing, and quality teams, and support compliant workflows.

Key Highlights

  • Understand how rheology supports pharmaceutical product development and manufacturing.

  • Use rheological measurements to optimize formulations and predict processability.

  • Apply rheological data to support scale-up, technology transfer, and QC.

  • Learn about relevant standards including USP <912>, USP <1912>, ISO 11040, and ISO 7886-1.

  • See practical application examples and a live instrument demonstration. 
     

Dr. Michael Toifl (Langues: English)

Lieu: Hyderabad, India, Anton Paar India - Hyderabad Office Hyderabad
Fin de l'inscription: 30 juil. 2026

Personne à contacter et inscription:
Mr. Vijaya Saradhi
Tél.: 9599600359
vijaya.saradhi[at]anton-paar.com