Part 3: Characterizing amorphous materials

The final event in our three-part series focuses on the characterization of amorphous materials.

Such forms of active pharmaceutical ingredient (API) gain increasing attention due to their improved solubility. However, it is vitally important to fully understand their stability behavior in order to ensure a reliable drug product (with sufficient shelf-life) can be realized.  In this case, a multi-technique approach including structural, thermal and morphological analysis should be adopted. Our experts will present case studies, demonstrating advantages of this way of materials characterization. 

You will also have the option to ask questions to our experts, Dr Gabriele Kaiser, Dr David Fengas and Dr Natalia Dadivanyan. If this time doesn’t suit you, register for the later session here

Join our upcoming series of "Everything pharmaceutical scientists need to know about solid form characterization"

  • Webinar 1: API selection. Register here
  • Webinar 2: Formulation and Process Development. Register here
  • Webinar 3: Characterizing amorphous materials


Tipo de medición:
Crystal structure determination
Phase identification
Phase quantification
November 17 2021 - November 17 2021
10:30 - 11:30
Eastern Time [US & Canada]
Tipo de evento:
Webinar - Live
Aeris range
Empyrean range
Mastersizer 3000
Morphologi 4
X-ray Scattering
X-ray Diffraction (XRD)
Laser Diffraction
Morphologically Directed Raman Spectroscopy (MDRS)
Differential Scanning Calorimetry (DSC)
Pharmaceutical formulation development
Drug discovery


What will you learn?

  • Expand your understanding of amorphous materials
  • Learn about monitoring the stability of amorphous materials
  • Learn about the impact of solid form transition of size and shape of API particles


  • Dr Gabriele Kaiser - Business Field Manager Pharmacy, Cosmetics and Food, Netzsch
  • Dr Robert Taylor - Product Technical Specialist, Malvern Panalytical
  • Dr Natalia Dadivanyan - Field Application Scientist X-ray Products, Malvern Panalytical

Preguntas más frecuentes

Who should attend?

  • Anyone involved in API development
  • Anyone engaged in stability assessment
  • Anyone developing pharmaceutical formulations