Artificial Intelligence & Cloud: Validation and Data Integrity in a BioPharma GxP Environment
This course is a compilation of topics representing recent challenges related to CSV of AI or cloud-based systems in a GxP regulated context, and how CSV relates to data integrity.
Advanced RBI for Process Industry
This course will provide inspectors and analysts with advanced knowledge and skills in Risk-Based Inspection (RBI) based on the framework defined in API RP 580 and an in-depth understanding of the calculations performed according to the API RP 581 for fixed equipment and piping.
Cross-Contamination Risk Assessment in Pharma Manufacturing
The training will share approaches how systematic risk management of cross-contamination risks can be performed and implemented in the QA system.
Pharmacovigilance Inspections & Audits Updates
This course will provide a comprehensive, yet practical guide to pharmacovigilance audits and inspections best practice to help navigate what is required to demonstrate compliance.
Well Completions and Interventions
This course uses 4 online half-day modules to provide an in-depth introduction to well
completions and interventions for the oil and gas industry.
Produced Water Treatment & Management
The course is presented by an independent consultant, well recognized in the petroleum industry, who has travelled around the world to provide assessments of water systems and treatment options and who is well-updated on the latest technologies under development and qualified by the industry.
CCUS Technologies – CO2 Capture, Processing and Storage
The use of fossil fuels will continue to be key for ensuring energy supply stability in the incoming decades.
High Tech Maintenance Management
This Modern Maintenance Management course provides an in-depth insight into understanding reliability and maintenance.
Well Plugging and Abandonment
This 4-day master-class seminar will cover in depth how and why wells are plugged and abandoned at the end of their useful life.
Monoclonal Antibodies
This unique 3-day course is designed for advanced persons & specialists in the field of protein therapeutics or participants who have emphasis to jump into this exciting new business field.
Toxicology, ADME & Early Drug Development Plan
Building an Integrated Safety Testing Strategy based on ADME and Toxicology. The purpose of this Toxicology, ADME & Early Drug Development Plan is to understand the concept of a combined ADME-Toxicology approach.
Good Laboratory Practice & GCP for Laboratories
This two-day course with workshop and case examples is designed for Managers and Sponsors of GLP and/or GCP Studies to develop a working knowledge of GLP and GCP requirements to support implementation of the Quality Management System in a GLP and/or GCP setting.
Gas Treatment and Sulphur Recovery
This course will take the participants through the different types of processes, describing how each functions and look at the strengths and weaknesses of each process.
Clinical Trials Quality & Inspection Updates
This practical course provides an in-depth understanding of current and planned GCP requirements and their practical implications as well as insights into the current GCP inspection focus and hot topics.
Quality & Regulatory Requirements for Inhalation Drug Products
This course will cover the aspects of the human respiratory tract that are relevant to the delivery of medicines to the lungs.
STO Planning & Scheduling
This course includes specific checklists, procedures, and strategies to improve your current shutdown planning, scheduling, and execution.
Advanced Protein Aggregation & Characterization
This practical Advanced Protein Aggregation & Characterization course provides an insight into the diversity of aggregates and particulates present in biopharmaceuticals revealed by new orthogonal methods.
Stability & Shelf Life of Cell & Gene Therapy Products
This 2-day practical workshop is focused on ATMPs & brings a comprehensive overview on stability and shelf-life regulatory landscape, as well as analytical methods for stability assessment of your cell & gene therapy products.
Big Data & Process Analytics
Data Science is one of the newest technologies that will bring significant benefits to Chemical Process plant Operation now and will become increasingly important in the near future.
Computerized Systems Validation, Data Integrity & Cloud Computing in Pharma & Biotech
This course is a compilation of topics representing recent challenges related to CSV of cloud-based systems in GxP regulated context, and how CSV relates to data integrity assurance.
