Rosa Terribile
Rosa Terribile is in QA at Mipharm and she is a member of the AFI process validation working group.
Articles
Enhancing Process Validation for Sterile Liquid and Freeze-Dried Forms: Part 1
Francesca Speroni;Ilaria Franceschini;Maurizio Valleri;Mauro Silvestri;Matteo De Nigris ;Simona Bertolini;Luca Rizzo ;Alessia Garavaglia ;Camillo Bologna;Rosa Terribile;Stefano Pompilio;Enrico Modena;Stefano Selva;Lorenza Broccardo;Cesare Armetti;Marco Adami
October 16th 2020AFI representatives of the process validation working group explore and define key elements for an enhanced approach to process validation for sterile liquid and freeze-dried forms.
Enhancing Process Validation for Solid Oral Dosage Forms: Part 2
Francesca Speroni;Ilaria Franceschini;Maurizio Valleri;Mauro Silvestri;Matteo De Nigris ;Simona Bertolini;Luca Rizzo ;Alessia Garavaglia ;Camillo Bologna;Rosa Terribile;Stefano Pompilio;Enrico Modena;Stefano Selva;Lorenza Broccardo;Cesare Armetti;Marco Adami
October 16th 2020AFI representatives of the process validation working group explore and define key elements for an enhanced approach to process validation for solid oral dosage forms.
Latest Updated Articles
Published: October 11th 2024 | Updated: October 18th 2024
Buy, Sell, Hold: Cell and Gene Therapy - Part 1
Published: September 10th 2024 | Updated: September 18th 2024
CPHI Milan Announces 2024 CPHI Pharma Award Finalists
Published: November 6th 2024 | Updated: November 19th 2024
Automate Aseptic Filling: Closing the System at Full Modularity
Published: November 5th 2024 | Updated: November 19th 2024
Untethered Data: Unifying and Contextualizing Drug Discovery Data
Published: November 8th 2024 | Updated: November 19th 2024
Application of Validation Principles to the Training Quality System: Part 9, Quality Risk Management Hazard Identification
Published: November 4th 2024 | Updated: November 19th 2024
Strategies for Overcoming Common Challenges in Tech Transfer
