2025 ISPE March Training
Deep Dive into Pharma Training Courses
Gain solutions to your company's immediate goals to lower production costs, improve process efficiency, increase production quality, and meet regulatory requirements.
- Real World Practice: Courses present exercises that use current problems and situations common to the industry.
- Experienced Instructors: Subject matter experts and top leaders in the pharmaceutical industry who have years of experience in their field of study.
- Global Training to Fit Your Needs: With eLearning
In-Person Training Events Online Live Training Events
In-Person Training Events
Advancing Pharmaceutical Quality (APQ) Quality Management Maturity
18 - 19 March 2025
In this training, you will be led through the APQ guide series for Quality Management Maturity including how to leverage structured tools using a tested industry best-practice approach to coordinating, conducting, presenting, and reporting out on assessment outcomes. You will learn how the APQ methodology is used to improve the current state of quality and how it can benefit your organization through the Assess, Aspire, Act, Advance Framework.
Training Venue:
6110 Executive Blvd Suite #600
North Bethesda, MD 20852
Instructors
Aseptic Processing & Annex 1
19 - 20 March 2025
In-person after the 2025 ISPE Aseptic Conference
This course will focus on aseptic processing and quality management around the most important pharmaceutical technology.
Training Venue:
2799 Richmond HWY
ARLINGTON, VA 22202, USA
Hotel & Reservations: +1 703-418-1234
Instructor
Online Live Training Events
Oral Solid Dosage Forms
4 - 7 March 2025
This training course examines current technology and provides scenario-based exercises for system troubleshooting and investigational events for process deviations, discusses quality management and GMP inspection preparation, and provides guidance on advanced asset lifecycle management strategy.
Instructor
Biopharmaceuticals: CMC Aspects
10 - 13 March 2025
This new instructor led course is an advanced level course on Chemistry, Manufacturing and Controls (CMC) aspects of biopharmaceutical development. The purpose of this course is to provide an advanced understanding of the CMC considerations of biopharmaceuticals from development to commercialization. An emphasis will be placed on using Quality by Design principles to develop, manufacture and guide the product lifecycle.
Instructor
Cleaning Validation Principles
24 - 27 March 2025
This course covers the risk-based approach to cleaning development and verification; risk analysis; procedures and evaluation tools including FMEA / FMECA, master planning, risk control, PAT, periodic assessment and monitoring, risk review and communication.
Instructor
Overview of Biopharmaceutical Manufacturing Processes
24 - 27 March 2025
Explore commonly used manufacturing process operations including cell culture and fermentation; harvest and recovery; viral removal and inactivation; purification processes such as tangential flow filtration, centrifugation, size exclusion, and adsorptive chromatography.
Instructor
Facility Project Management
25 - 28 March 2025
This course will focus on aseptic processing and quality management around the most important pharmaceutical technology.
Instructor
