Trainings
Here are some of our upcoming events:
Planning and Scheduling Shutdowns and Turnarounds
This course will explain the efficient shutdown & turnaround management process step by step with deep insights and important guidelines/best practices. You’ll learn the concepts associated with the successful planning and execution of major plant shutdowns. You’ll gain competence in the use of modern, well proven approaches, tools and techniques to achieve the desirable end result.
#Oil&gas/Energy
ADVANCED MAINTENANCE MANAGEMENT
This course is designed for all Maintenance Managers/Engineers, Supervisors, and Planning
Engineers. It is also suitable for those in operations, engineering, and purchasing/materials
divisions and who would like to understand how the quality of the maintenance function
affects their department, and their organization's bottom line.
#Oil&gas/Energy
Granulation & Tabletting
The training content is intended to impart sufficient knowledge and understanding of the manufacturing process to enable the participants to be proficient in their work environment. This three-day course covers relevant information with regards to wet granulation, granule drying, the tableting process, the automation of the press, tablet fault finding, tablet defects, ancillary equipment, IPC testing, granule particle size testing, and scale up concerns.
#Pharmaceuticals/Biopharmaceuticals
Analytical Methods Validation
The training content is designed to learn on how to design efficient and practically
relevant experimental validation, verification, and transfer studies, to calculate suitable performance parameters, to learn how to optimise the precision of the reportable result by a scientifically based replication strategy, to learn how to derive suitable acceptance criteria, to get an overview on USP and Ph.Eur. General chapters on verification of Compendial procedures, and on analytical transfer guidelines.
#Pharmaceuticals/Biopharmaceuticals
Data Analysis to Understand the performance of analytical procedures
The training content is designed to learn on how to design efficient and practically
relevant experimental validation, verification, and transfer studies, to calculate suitable performance parameters, to learn how to optimise the precision of the reportable result by a scientifically based replication strategy, to learn how to derive suitable acceptance criteria, to get an overview on USP and Ph.Eur. General chapters on verification of Compendial procedures, and on analytical transfer guidelines.
#Pharmaceuticals/Biopharmaceuticals
