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Design, Qualification and Operation of HVAC Systems in Pharma This eLearning module discusses the need for HVAC systems in pharmaceutical plants, and its role in ensuring optimum conditions for product and personnel safety through temperature, dust and contamination control. 0.00 10/08/2020 21/08/2020 18
Equipment qualification and life cycle management This module is designed to introduce users of various pharmaceutical industry equipment to the different stages of equipment qualification such as design, installation, performance and general operations. 0.00 10/08/2020 10/08/2020 18
Water for Pharmaceutical Purposes: Generation and Quality Control This comprehensive eLearning module covers the fundamentals of pharmaceutical water systems designs, water quality testing and system validation processes, including Water for Injection (WFI). 0.00 05/08/2020 21/08/2020 18
An Interactive Guide to Good Warehouse Practice This exhaustive eLearning module on Good Warehousing practices gets you into the warehouse to investigate what works and what does not. 0.00 05/08/2020 21/08/2020 19
Covid-19 Preparedness: Getting Back to Work This eLearning module incorporates many short videos to educate employees on physical distancing, temperature checks, hygiene, and company policies, as they return to work after COVID associated lockdowns. 0.00 20/08/2020 20/08/2020 19
Intellectual Property: What is IP, and how to protect it This module is designed as an introduction you to Intellectual Property (IP) in the Pharmaceutical industry. It delves into the various types of IP, means of protection and how to design company policies around Intellectual Property. 0.00 05/08/2020 21/08/2020 19
10 golden rules of GMP This module reviews the good manufacturing practices (GMP) required in facility design and equipment, their upkeep, and the impact of quality-by-design on processes. It also reviews the importance of GMP in personnel training, role definitions, hygiene, and internal audits. 0.00 10/08/2020 12/08/2020 17
A Beginner's Guide to Process Validation This module focuses on the practical applications of the lifecycle approach to all stages of Process Validation (PV). It provides insight into regulations guidance, and best practices around PV utilized across the industry.. 0.00 20/08/2020 20/08/2020 17
A Complete Guide to Environmental Monitoring This module provides an in-depth review of the regulatory requirements of environmental monitoring (EM) of cleanrooms, parameters to be monitored and the tools and techniques used for environmental monitoring. 0.00 10/08/2020 21/08/2020 17
An Interactive Guide to Good Documentation Practice This module is designed to review some aspects related to creation, implementation, archiving, storage and destruction of documents in GxP environments. It goes onto discuss common failures in good documentation and steps to ensure integrity of data generated 0.00 05/08/2020 21/08/2020 17
Applications of Crystallization in API Manufacturing Crystallization is a purification technique involving solid formation. This modules covers crystallization in detail, and solution crystallization in particular. It also looks at factors affecting solution crystallization like concentration and temperature. 0.00 05/08/2020 21/08/2020 17
Aseptic Processes and Cleanroom Basics This eLearning module focuses on concepts of contamination, basic design of cleanrooms, their monitoring and manufacturing of aseptic products. 0.00 10/08/2020 21/08/2020 17
Cleanroom Design and Control of Contamination Cleanrooms are important parts of facilities that make sensitive products like pharmaceuticals, and semi conductors. This eLearning module explores how personnel and other sources of contamination impacts the final product. , and how to behave appropriately in a clean room to maintain sterile environment 0.00 10/08/2020 21/08/2020 17
Equipment Logbooks: Good Practices and Regulatory Requirements This eLearning module covers the regulatory expectations and practice related to equipment logbooks. 0.00 05/08/2020 21/08/2020 17
Maintaining Data Integrity in GMP Environments This eLearning module reviews the importance of data integrity in drug manufacturing, common failures in data integrity, and the necessary steps that must be taken to ensure integrity of the data generated at pharmaceutical organizations. 0.00 10/08/2020 21/08/2020 17
Overview and Classification of Topical Dosage Forms This eLearning module is designed to explain what topical medication is, and why topical dosage forms are preferred. The module also categorizes different dosage forms based on their physical properties, and formulation bases. 0.00 05/08/2020 21/08/2020 17
Overview of GMP and Quality Concepts in Pharmaceuticals and Biotechnology This module covers the basics of Good Manufacturing Practice (GMP) including the importance of following personal hygiene and data integrity in the drug companies. 0.00 20/08/2020 20/08/2020 17
Personal Hygiene in GMP Environments This eLearning module reviews hygiene and sanitation at the workplace including personnel, premises, equipment, apparatus, processes, and raw materials. It investigates all sources of contamination of the final product, with a primary focus on personal hygiene. 0.00 10/08/2020 21/08/2020 17
Personnel Qualification and training in GxP environments The eLearning module looks at the key principles of training and development, and the different types of training methods in GxP environments. It also reviews the various stages of training in a typical biotech or pharmaceutical organization. 0.00 10/08/2020 21/08/2020 17
Process Filtration in the API Industry. Filtration is the process through which the active ingredients are separated from byproducts after a chemical reaction. This e-module explains the “what”, “why”, and “how” of process filtration in API manufacturing 0.00 10/08/2020 10/08/2020 17
Understanding the "Why" and "How" of GMP Audits This GMP course is specifically designed to explain the fundamental concepts of GMP auditing for the pharmaceutical industry, including regulatory audits and self inspections. 0.00 10/08/2020 21/08/2020 17
A Practical Guide to pH Measurement and Controls This eLearning module explores pH and why measuring it accurately is essential during drug manufacturing, The module also provides an overview of the proper controls and procedures to use a pH meter and associated probes, 0.00 10/08/2020 21/08/2020 8
A Practical Guide to Sample Preparation Techniques - Part 1 Part 1 of this two-part module covers the basics of sample preparation focusing on weighing, crushing and grinding, sonication, shaking, dilutions and glassware handling 0.00 20/08/2020 20/08/2020 8
A Practical Guide to Sample Preparation Techniques - Part 2 Part 2 of this two-part module covers the basics of sample preparation focusing on pipetting, filtration, centrifugation and vial filling. 0.00 20/08/2020 20/08/2020 8
A Practical Guide to Titrations in Quality Testing This module looks at the basics of potentiometric and Karl Fischer titrations. It provide an overview of the components of an autotitrator and different titration methods. 0.00 20/08/2020 20/08/2020 8
Atomic Absorption Spectrometry and its Applications The module covers the basic principles of atomic absorption spectroscopy and provides an overview of the components and operation of the spectrometer . 0.00 20/08/2020 20/08/2020 8
Disintegration Testing of Oral Solid Dosage Forms This module answers the “why” and “how” of a disintegration test, and best practices to follow while performing disintegration testing. 0.00 20/08/2020 20/08/2020 8
Dissolution Testing of Oral Solid Dosage Forms The module looks at dissolution testing as a proxy for the bioavailability of a drug in human body. It also provides an overview of the components and operation of the dissolution apparatus 0.00 20/08/2020 20/08/2020 8
Drying of pharmaceuticals: Theory and Practice This module gives an overview of the fundamental principles of drying as well as terms commonly used in drying processes. It also explores novel drying technologies. 0.00 20/08/2020 20/08/2020 8
Fourier Transform Infrared Spectroscopy and its Applications This eLearning module is a comprehensive review of IR spectroscopy - used for identification of molecules by utilizing their vibrational properties. 0.00 20/08/2020 20/08/2020 8
Gas chromatography and its Applications This eLearning module is an introduction to gas chromatography. It delves into identification and separation techniques based on component volatility and polarity. 0.00 10/08/2020 21/08/2020 8
Halogen Moisture Analysis (HMA) and its Applications This module covers the principles and basics of moisture determination using Halogen Moisture Analyzer. It provides a visual guide to the components and operation of an analyzer. 0.00 20/08/2020 20/08/2020 8
Handling Out-of-Specification (OOS) Events This eLearning module is designed to provide essential training for conducting Out of Specification (OOS) investigations in GMP environments. 0.00 20/08/2020 20/08/2020 8
Handling Product Complaints and Recall In this eLearning course you will learn all relevant aspects of complaint handling and recall system as per current GMP requirements in the pharmaceutical industry. 0.00 10/08/2020 06/09/2020 8
HPLC and its Applications This GMP course is designed to explain the fundamental concepts of HPLC, a technique used to separate individual compounds in a mixture by passing a highly pressurized solvent containing the mixture through a column filled with a solid adsorbent material 0.00 10/08/2020 21/08/2020 8
Melting Point Determination and its Applications This module reviews the basics of melting point determination, its applications, and the operation and best practices for its measurement 0.00 20/08/2020 20/08/2020 8
Particle Size Analysis and its Applications This eLearning module explores the principles of particle size analysis, especially using the Malvern instrument. It will also provide an overview of components and operation of the analyzer. 0.00 20/08/2020 20/08/2020 8
Pharmaceutical Applications of the Distillation Process This eLearning module covers the distillation process in API manufacturing - fundamental theory to applications to its applications. 0.00 20/08/2020 21/08/2020 8
Refractive Index and its Applications This module is an introduction to the concepts of refraction, refractive index and its application in determining the purity of substances. 0.00 20/08/2020 20/08/2020 8
Semi Solid Dosages: Manufacturing and Quality Evaluation This eLearning module covers the properties and manufacturing methods of high quality semi solid dosage forms through structured development and a process design approach. 0.00 20/08/2020 20/08/2020 8
Specific Optical Rotation and its Applications This module is to understand the basics of Specific Optical Rotation (SOR) and principle of polarimetry. It gives and an overview of the components and operation of a polarimeter. 0.00 20/08/2020 20/08/2020 8
Thermal analysis by Differential Scanning Calorimetry (DSC) The module looks DSC and its application in measurement of thermal transitions in samples. It also provides a visual guide to the operation of a typical differential scanning calorimeter. 0.00 20/08/2020 20/08/2020 8
Understanding Stability Testing of Biological Products This eLearning module reviews the regulatory guidelines specific to biologics. Biotechnological drugs need to be managed differently from chemical drugs as they are complex, more sensitive, and require extensive testing. 0.00 10/08/2020 21/08/2020 8
UV Absorption Spectroscopy and its Applications This module is on Ultraviolet (UV) Visible absorption spectroscopy: a spectro-analytical procedure for the quantitative determination of compounds containing chromophores that absorb UV. 0.00 20/08/2020 20/08/2020 8
X-Ray Diffraction and its Applications This eLearning module is on the basic principles and applications of X-Ray Diffraction - a technique used in the study of crystal structures, and atomic spacing. characterization 0.00 20/08/2020 20/08/2020 8
A Beginner’s Guide to Biosimilarity This eLearning module reviews the fundamental concepts of of biologics and biosimilars. It investigates how biologics are different from chemical drugs and generics. It also looks at manufacture and evaluation of biosimilars, and their safety and efficacy comparison with the innovator drugs. 0.00 10/08/2020 21/08/2020
An Interactive Guide to Good Clinical Practice This eLearning module reviews the basics of GCP, an ethical and scientific quality standard that assures that clinical data and results are credible and accurate, and that the rights, integrity and confidentiality of trial subjects are respected. 0.00 10/08/2020 21/08/2020
An Interactive Guide to Good Laboratory Practice This eLearning module reviews basics of GLP, and provides a historical background on how and why Good Laboratory Practices were introduced, and documented. 0.00 10/08/2020 21/08/2020
Maintaining Safety in Laboratory: A Practical Guide This eLearning module helps in identifying health and safety hazards in a pharmaceutical laboratory. It delves into procedures and systems that ensure a safe working experience in a laboratory, and the steps that must be followed to avoid hazardous exposures 0.00 10/08/2020 21/08/2020
Permit to Work (PTW) and Maintaining a Safe Workplace This eLearning module answers when and why a PTW is needed in pharmaceutical set-ups. It also looks at and how PTW helps mitigate risks at the workplace., and typical procedures to be followed to raise a PTW. 0.00 20/08/2020 21/08/2020