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.
Corrosion Under Insulation
The most complete and comprehensive CUI course in the market running since 2014. Your guide to understanding and managing CUI.
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.
Quality & Regulatory Requirements for Drug Device Combination Products in the UK & US
This interactive course will bring clarifications on quality & regulatory requirements for combination products in the UK & US.
Well Integrity Management
This 4-day master-class seminar will provide a comprehensive, in-depth introduction to the discipline of well integrity, and discuss in detail how we can achieve it effectively and efficiently during the design and operational phases, as well as after wells are abandoned.
Lipid Nanoparticles for Drug/mRNA Delivery
After the successful development of lipid nanoparticles (LNPs) comprising messenger RNA (mRNA) for vaccination against Covid-19, the interest in mRNA and nanoparticle systems for various therapeutic applications has surged tremendously.
Well Integrity Management for Geothermal Wells
This 4-day master-class workshop will provide a comprehensive introduction to the discipline of well integrity as it applies to geothermal wells.
Pharma & Biotech CSV in the Cloud (IaaS/PaaS/SaaS)
This course is meant to be an advanced CSV course focusing on selected topics where validating cloud-based systems differ from on-premise solutions.
Technical Safety Management
The purpose of this 3-day training course is to highlight the safety life cycle pathway from initial major accident hazard identification through to long term sustained and safe operation of a process where a safety instrumented system(s) provides a layer of protection.
MIC (Microbiologically Influenced Corrosion) in Oil Production, Pipeline and Storage Facilities
Join this course to learn about the best practices to identify and control the MIC in your assets and facilities.
Quality & Regulatory Requirements for Biosimilars in the EU
The training aims to create deeper understanding why biotechnological products – and as a consequence Biosimilars – are a unique product category and what aspects have to be considered in R&D and Drug Regulatory Affairs.
Gas Chromatography in Oil & Gas Industry
The course covers all the elements of gas chromatography technique, from sample preparation and introduction, separation and detection systems.
