Showing all 92 results
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Aerosol Inhalers
PUF-1205An overview of the essential elements of aerosol inhalers, focusing on their purpose, key ingredients, benefits, limitations, typical… -
Anatomy of a Clinical Trial
CTM-1102An overview of the clinical trial process, from planning through closeout, this module delves into the design and… -
API Contamination Prevention
BGB-1203A comprehensive overview of the various types of contamination that can affect Active Pharmaceutical Ingredients (APIs) during production,… -
Basic Microbiological Techniques
PPM-1210An overview of essential microbiological techniques frequently performed in laboratory settings, emphasizing the preparation of different types of… -
Basic Microbiology
PST-1200Microorganisms and their threat to pharmaceutical and biologics products. It covers types of microorganisms, sources of contamination, and… -
Buildings & Facilities
PGI-1290An overview of the foundational principles of GMP-compliant pharmaceutical plant design, focusing on minimizing contamination risk through strategic… -
Centrifuges
PEA-1210An introduction to the theory and operation of centrifuges in API manufacturing, focusing on the principles behind batch… -
Chemical Laboratory Waste
PSY-1260A comprehensive guide to the categorization, storage, and safe disposal of chemical waste produced in pharmaceutical and laboratory… -
Chemical Reactions: Overview
PUA-1200An overview of chemical reactions in API (Active Pharmaceutical Ingredient) manufacturing, with a focus on controlling key process… -
Chemical Reactions: Properties
PUA-1201An in-depth look at the key physical and chemical properties that are critical for monitoring and controlling chemical… -
Chemical Reactor Design
PEA-1200An exploration of the design and operational principles of chemical reactors used in the production of Active Pharmaceutical… -
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… -
Crystallization
PUA-1220An introduction to the principles and techniques of crystallization used in API manufacturing. This module covers the formation… -
Dissolution Equipment Set-Up
PPL-1212Master the essential steps for preparing solutions and setting up equipment for the dissolution process. This module covers… -
Dissolution Testing
PPL-1213A comprehensive guide to the practical aspects of dissolution testing, covering the essential steps from setting operational parameters… -
Distillation & Reflux
PUA-1210The principles of distillation and reflux, focusing on their roles in active pharmaceutical ingredient (API) manufacturing. Learners will… -
Dosage Form Introduction
PUF-1201Explore the fundamentals of pharmaceutical dosage forms, including solids, liquids, aerosol inhalers, semisolids, and transdermal patches. Discover how… -
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,… -
Executive Responsibility in Pharma Manufacturing
RGM-1200This module provides executive management in pharmaceutical manufacturing with a comprehensive understanding of their legal and regulatory responsibilities… -
Filtration
PUA-1240An introduction to the filtration process in API (Active Pharmaceutical Ingredient) manufacturing, covering the theory behind filtration, the… -
Filtration for Finished Dose
PEF-1204An overview of filtration in pharmaceutical manufacturing with a focus on the plate and frame filter press. Learn… -
Finished Dose Contamination Prevention
PGB-1203An overview of how contamination can threaten the safety and effectiveness of finished dose drug products. This module… -
Fluidized Beds
PEF-1206An overview of the fluidized bed granulation process, explaining its purpose, equipment, and the steps involved in forming… -
Fundamentals of Process Validation
PVF-1130An overview of process validation in regulated industries, such as pharmaceuticals, biopharmaceuticals, active pharmaceutical ingredients, and medical devices.… -
Gas Sterilization
PST-1295Ethylene oxide (ETO) use in gas sterilization, covering applications, process, equipment, and critical sterilization parameters. It also explores… -
GCP Essential Documents: Investigators Brochure & Study Protocol
CTM-1202An overview of two key documents used in a clinical trial – the Investigator’s Brochure and the Study… -
General Safety Hazards in the Microbiology Lab
PSY-1221Gain a comprehensive understanding of the critical safety hazards in a microbiology laboratory, from the handling of various… -
GLP – An Introduction
PGL-1220Provides personnel with a foundational understanding of Good Laboratory Practice (GLP), focusing on its significance in nonclinical laboratory… -
GLP – Working in the Laboratory
PGL-1221Gain a comprehensive understanding of Good Laboratory Practice (GLP) and its critical role in nonclinical studies. This module… -
GMP for APIs
BGB-1101Explores the foundations of Good Manufacturing Practices (GMP) in Active Pharmaceutical Ingredient (API) manufacturing, covering its historical development,… -
GMP for Finished Dose Forms
PGB-1101A foundational exploration of Good Manufacturing Practices (GMP) in the pharmaceutical industry, focusing on the historical events that… -
GMP for Microbiology
PGM-1200Explore the critical application of Good Manufacturing Practices (GMP) within a microbiology laboratory setting. This comprehensive module covers… -
GxP Computerized Systems Validation
CSV-1101An overview of the critical concepts and key requirements of Computerized Systems Validation (CSV) in regulated life sciences… -
HVAC and Cleanrooms
PST-1210Use of HVAC systems and HEPA filters in cleanroom environments. It covers the regulation of airflow, pressure, temperature,… -
In Vitro Dissolution
PPL-1211An in-depth overview of the in vitro dissolution testing process used in pharmaceutical laboratories. This module covers the… -
Instrumentation – Error Prevention
PPL-1205Gain essential knowledge on how to minimize errors when using spectrometry and pH measurement techniques in an analytical… -
Introduction to Microscopy
PPM-1211An essential overview of the role of microscopy in microbiology, this module details microscope components, lens systems, and… -
Introduction to Staining
PPM-1212Discover the essential techniques for preparing and staining bacterial smears to aid in the study and identification of… -
IT Use in Regulated Industries
GVC-1200Explore the critical role of Information Technology in the life sciences industry, from foundational concepts of IT systems… -
Laboratory Equipment Qualification
PVL-1200Gain a comprehensive understanding of laboratory equipment qualification, focusing on the critical stages that ensure accuracy, reliability, and… -
Laboratory GMP
PGL-1210Gain a comprehensive understanding of analytical laboratory Good Manufacturing Practice (GMP) requirements and their significance in maintaining the… -
Laboratory Information Management System
PGL-1206Explore the purpose and functionality of Laboratory Information Management Systems (LIMS) used in analytical laboratories. This module delves… -
Laboratory Safe Work Practices
PSY-1241An essential guide to ensuring safety in the chemical laboratory, focusing on the use of documented safety information… -
Liquid Dosage Forms
PUF-1204An overview of the essential characteristics, production methods, and practical considerations of liquid dosage forms, including solutions and… -
Method Validation Parameters
PVL-1210A comprehensive examination of the key parameters in analytical method validation, crucial for ensuring the accuracy and reliability… -
Moist Heat Sterilization
PST-1291An introduction to the principles and practices of moist heat sterilization using autoclaves. This module explains the science… -
New Drug Development and Clinical Trials
CTM-1100An essential overview of the drug development process, guiding learners through the stages from initial research to regulatory… -
Out of Specification and Atypical Results
PGL-1200An in-depth look at Out of Specification (OOS) and Atypical results in pharmaceutical quality control. It examines the… -
Overview of 21 CFR Part 11
GVC-1202Gain a clear understanding of the FDA's 21 CFR Part 11 regulation, which governs the use of electronic… -
Overview of GxP
GXP-1200The essential principles and regulations of Good Laboratory Practice (GLP), Good Clinical Practice (GCP), and Good Manufacturing Practice… -
Overview of Pharmaceutical Manufacturing
PGB-1100An overview of the foundational principles of pharmaceutical manufacturing, covering the different types of pharmaceutical products and the… -
Personnel and Training
PGI-1110An introduction to the roles, responsibilities, and regulatory requirements of personnel in pharmaceutical manufacturing environments. The module explains… -
Primary Packaging
PGI-1271An overview of primary packaging processes in pharmaceutical manufacturing, covering essential components such as container types, contamination prevention,… -
Principles of Good Aseptic Technique
PPM-1200The fundamentals of aseptic techniques are essential for microbiological testing in pharmaceutical and biologics environments. Learn how to… -
Process Flow Diagrams
PUA-1260An introduction to Process Flow Diagrams (PFDs) used in the pharmaceutical and chemical industries to visually represent processes… -
Reciprocating Pumps
PEA-1240An overview of reciprocating pumps, focusing on their functionality, types, and applications in chemical and pharmaceutical processing. It… -
Records in API Manufacturing
BGI-1101Effective record-keeping is a critical aspect of API manufacturing operations. This module introduces the essential records used in… -
Records in Finished Dosage Form Manufacturing
PGI-1101An overview of the essential role of records in Finished Dosage Form Manufacturing, focusing on their purpose, types,… -
Regulation of the Pharmaceutical Industry
PGB-1102Explore how the pharmaceutical industry is regulated across major global drug markets, focusing on key regulatory authorities, the… -
Roles and Responsibilities under ICH GCP
CTM-1101An exploration of the principles and guidelines outlined in ICH Good Clinical Practice (GCP), focusing on the ethical… -
Rotary and Centrifugal Pumps
PEA-1241A focused exploration of rotary and centrifugal pumps, their operational principles, and their application in pharmaceutical processing. This… -
Secondary and Tertiary Packaging
PGI-1272An overview of the procedures and protocols involved in secondary and tertiary packaging in pharmaceutical manufacturing. This module… -
Semisolid Dosage Forms
PUF-1203An overview of semisolid dosage forms used in the pharmaceutical industry, including ointments, creams, gels, and pastes. Learners… -
Solid Dosage Forms
PUF-1202An introduction to the various types of pharmaceutical solid dosage forms, including tablets, capsules, and sachets. The module… -
Solution Preparation
PPL-1202A detailed guide to accurate solution preparation in analytical laboratories, covering essential techniques for preparing quantitative solutions from… -
SOPs in API Manufacturing
BGI-1100Explores the essential role of Standard Operating Procedures (SOPs) in Active Pharmaceutical Ingredient (API) manufacturing. It focuses on… -
SOPs in Finished Dosage Form Manufacturing
PGI-1100An overview of the critical role of Standard Operating Procedures (SOPs) in Finished Dosage Form Manufacturing. This module… -
Staining Techniques
PPM-1213Gain a detailed understanding of various microbiological staining techniques, essential for observing and identifying microorganisms. Delve into simple… -
Sterile Filtration
PST-1293An overview of sterile filtration in the pharmaceutical and biologics industries, explaining the principles and applications of this… -
Tablet Coater
PEF-1208An overview of the tablet coating process, explaining its purpose, equipment, and the steps involved in coating tablets.… -
Tablet Press
PEF-1207An introduction to the essential principles of tablet compression, focusing on the critical process of tablet formation, the… -
Understanding Dissolution
PPL-1210Explore the fundamentals of dissolution testing and its critical role in the pharmaceutical industry. This module provides a… -
Unknown Bacterial Identification
PPM-1230Dive into the essential methods for identifying unknown bacterial contaminants within pharmaceutical and biologics laboratories. This module covers… -
Warehousing
PGI-1220An overview of the essential functions of warehousing within pharmaceutical and biologics facilities, emphasizing its role in maintaining… -
Water Impurities & Treatment
PUA-1251An essential guide to understanding the various impurities found in water used in pharmaceutical manufacturing. It covers the… -
Water Types and Testing
PUA-1250An overview of the different grades of water used in pharmaceutical manufacturing, including Potable Water, Purified Water, and… -
Wet Chemistry
PPL-1206A comprehensive overview of essential wet chemistry techniques, focusing on skills that ensure accuracy in laboratory analysis. It… -
Working with Reactors
PEA-1201The key processes involved in the operation of reactors, including proper techniques for weighing, charging, and taking samples.…
