Regulatory Requirements for Membrane Filtration / Annex 1
This module provides an overview of the regulatory landscape applicable for filters in biopharmaceutical processes, as well as the requirements for filter validation
Who Should Attend
This training is primarily directed to production managers, quality control managers and validation managers
Course Overview
Our face-to-face training consists of theoretical as well as practical parts covering regulatory guidelines for filter testing and validation, with a special emphasis on the new EU GMP Annex 1 and the special requirements of PUPSIT in single-use processes as well as re-usable systems
Venue of the course: Language: Course Dates: | Training Hours: Training Fees: Type of Training: |
* For bundle option please indicate your course selection under "My Request" on the Registration Form below.
Venue of the course: Language: Course Dates: Mar 06, 2025 (English) | Training Hours: Training Fees: Type of Training: |
* For bundle option please indicate your course selection under "My Request" on the Registration Form below.
Venue of the course: Sartorius Application Center, Singapore Language: English Course Dates: Mar 20, 2025 | Training Hours: Day 3 of a 3-day training Training Fees: Three-day filtration course, combined with the Dead-End Filtration and Integrity Testing - 2250 SGD per person plus taxes Type of Training: Classroom Training |