Sterile products processing relates to how sterile drug products are manufactured using aseptic (or free from contamination) process methods where the drug substance, excipients, and vehicle (e.g., saline or water for injection) are combined and filled into a container (such as a syringe)
Video
Medical Device Sterilization with FDA
Medical Device Sterilization with FDA Complimentary Learning Level: Intermediate/Advanced Session…
iSpeak Blog
New ISPE Guide Highlights Best Practices and Benefits of Unique Identification of Glass Containers
Although parenteral products make up only 1% of global pharmaceutical prescriptions by volume, at…
PE Articles
Continuous Buffer Management System: Large-Scale Buffer Preparation
Content originally published in Pharmaceutical Engineering® May/June 2024, Volume 44, Number 3…
PE Articles
A Guide to Unique Identification of Glass Primary Containers
The new ISPE Good Practice Guide: Unique Identification of Glass Primary Containers in…
PE Articles
Fulfilling Annex I in Sterile Drug Production: When to Use Automatic Loading and Unloading Systems for Freeze Dryers
Sterile drug production has always been a challenging task to perform in the pharmaceutical industry…
Product
Good Practice Guide: Unique ID of Glass Primary Containers
Published: May 2024 Pages: 86 Table of Contents Special Pricing for Emerging Economies Many current…
PE Articles
Continuous Buffer Management System: Large-Scale Buffer Preparation
Although traditional tank farm systems have long been the cornerstone of buffer preparation, they…
iSpeak Blog
Empowering the Aseptic Workforce: Training and Continuous Learning as an Enabler for Success
In the pharmaceutical industry, which is highly regulated, aseptic processing is a critical…
iSpeak Blog
ATMP Cleanroom Facilities: A Roadmap for Success
What is the Route to Successful ATMP Cleanroom Development? Mitch Gonzales, Vice President of…
iSpeak Blog
Pharma 4.0 Enabling Technologies: Use Cases, Benefits and Constraints
At the 2023 ISPE Pharma 4.0™ & Annex 1 Conference in Barcelona, Spain and virtual, Track #6 will…
iSpeak Blog
Eco-friendly Pharma: Sterilization and Sustainable Practices
In the intricate world of pharmaceuticals, where precision and safety are paramount, the marriage of…
Video
Implementing X-Ray for Single-Use Systems Sterilization: Current Status
Complimentary Learning Level: Basic/Intermediate Session Length: 1 hour Sterilization by gamma…
Guidance Documents
Manufacturing Operations (1)
Microbiological & Viral Contamination Control (1)
Community Discussions
Community Discussions
Nov 14, 2024
Sustainable Facilities, HVAC, & Controlled Environments
Manufacturing Operations
Nov 04, 2024
Information Systems
Management
Pharma 4.0™
Project Management
Nov 04, 2024
Regulatory
Supply Chain
Active Pharmaceutical Ingredients
Good Manufacturing Practice
Nov 03, 2024
Women in Pharma®
Nov 02, 2024
GAMP®
Lifecycle Management
Oct 31, 2024
Regulatory
Quality
Good Manufacturing Practice
Sustainable Facilities, HVAC, & Controlled Environments
Oct 30, 2024
Validation
Webinars
iSpeak Blog Posts
Pharmaceutical Engineering® Magazine
A Guide to Unique Identification of Glass Primary Containers
The new ISPE Good Practice Guide: Unique Identification of Glass Primary Containers in…
Continuous Buffer Management System: Large-Scale Buffer Preparation
Although traditional tank farm systems have long been the cornerstone of buffer preparation, they…
Enhanced Intervention Detection in Aseptic Fill Using AI/ML
We will show how continuous, real-time capturing of data with immediate data analysis by an ML…
Communities of Practice Profiles: Meet the Sterile Products Processing CoP
The members of the Sterile Products Processing (SPP) Community of Practice (CoP) Steering Committee…
Message From the Chair: Heading Toward a New Annex 1 and ISPE Annual Meeting
Summer is over and we are all back to our workplaces. This year has been different than the two…
Validation of Aseptic Processes Using Media Fill
Aseptic process simulation (APS) is essential for validation of an aseptic manufacturing process and…
Safeguarding Vial Container Closure Integrity: A Systematic Approach
Any systematic pharmaceutical engineering approach for ensuring vial container closure system (CCS)…
2021 ISPE Aseptic Conference Regulatory Panel
The 30th ISPE Aseptic Conference culminated in the interactive regulatory panel, which offered…
ISPE Aseptic Conference Turns 30
The ISPE Aseptic Conference will celebrate its 30th year with the virtual conference on 15–17 March…
Using CFD Multiphase Modeling to Predict Bioreactor Performance
Computational fluid dynamics (CFD) can reduce or eliminate the need to perform bioreactor scale-up…
2020 ISPE Barrier Survey: Tracking the Journey of Barrier Technology
For over two decades, the ISPE Barrier Isolator Survey has gathered meaningful data on the…
Videos
Professional Development Training
Aseptic Processing & Annex 1 Training Course
This course will focus on aseptic processing and quality management around the most important pharmaceutical technology.
White Papers
September / October 2024
PIC/S in Latin America: Harmonization of cGMP Procedures Cover: This article offers an overview of…
July / August 2024
The explosive growth of advanced therapy medicinal products (ATMPs), particularly cellular…
May / June 2024
The commercialization of personalized medicine has ushered in demand for a new type of facility—…
