Preventing Contamination in Manufacturing
Showing all 22 results
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API Contamination Prevention
BGB-1203A comprehensive overview of the various types of contamination that can affect Active Pharmaceutical Ingredients (APIs) during production,… -
Aseptic Processing – Working with Closed Isolators
ASP-1107A detailed look at the use of closed isolators in aseptic processing of sterile products, covering their design,… -
Aseptic Processing: Cleanrooms and Control Technologies
ASP-1102Cleanroom design, use, and operation in aseptic processing, and the role of associated contamination control technologies such as… -
Aseptic Processing: Concepts and Controls
ASP-1101Aseptic processing concepts and associated technologies and techniques used for contamination control and prevention, including procedures to minimize… -
Aseptic Processing: Contamination Control
ASP-1104Contamination prevention measures, procedures, and practices that are typically implemented in aseptic processing including the use of cleanrooms,… -
Aseptic Processing: Decontamination and Sterilization Technologies
ASP-1105Methods typically used to decontaminate and sterilize equipment, consumables, containers/closures, and products as part of aseptic processing. Methods… -
Aseptic Processing: Essential Personnel Practices
ASP-1108In depth exploration of essential personnel practices in aseptic processing, presented through the manufacturing journey of a fictional… -
Aseptic Processing: Gowning
ASP-1103Gowning and its use in aseptic processing, including the different gowning requirements for different cleanroom classifications, the protective… -
Aseptic Processing: Working with Biosafety Cabinets
ASP-1106Principles of working with biosafety cabinets focusing on the role of Class II BSCs in contamination prevention. It… -
Clean in Place
BPU-1101Explains key concepts of Clean In Place (CIP) technology commonly used in the biotechnology and pharmaceutical industries. It… -
Cleaning of Equipment
PGI-1230An overview of essential cleaning practices for equipment in pharmaceutical and biologics manufacturing. This module explains the importance… -
Cleanrooms: Rules, Control Parameters, and Testing
PST-1265Rules, control parameters, and testing methods for cleanrooms used in pharmaceutical and biologics manufacturing facilities. It covers good… -
Contamination Control Strategy – Annex 1 and QRM
CCS-1101Explains the ‘why’ behind Contamination Control Strategy (CCS) and Quality Risk Management (QRM) for all employees involved in… -
Contamination Control Strategy – QRM in Practice
CCS-1102Unlocks the ‘how’ of using Quality Risk Management (QRM) to successfully devise, implement, and maintain your facility’s Contamination… -
Dress Codes for APIs
BGB-1204A detailed guide to the importance and implementation of dress codes in Active Pharmaceutical Ingredient (API) manufacturing. It… -
Dress Codes for Finished Dosage Form Manufacturing
PGB-1204An overview of contamination prevention in finished dose pharmaceutical manufacturing, highlighting the types and sources of contamination—microbiological, physical,… -
Finished Dose Contamination Prevention
PGB-1203An overview of how contamination can threaten the safety and effectiveness of finished dose drug products. This module… -
Gas Sterilization
PST-1295Ethylene oxide (ETO) use in gas sterilization, covering applications, process, equipment, and critical sterilization parameters. It also explores… -
HVAC and Cleanrooms
PST-1210Use of HVAC systems and HEPA filters in cleanroom environments. It covers the regulation of airflow, pressure, temperature,… -
Moist Heat Sterilization
PST-1291An introduction to the principles and practices of moist heat sterilization using autoclaves. This module explains the science… -
Sterile Filtration
PST-1293An overview of sterile filtration in the pharmaceutical and biologics industries, explaining the principles and applications of this…
