Materials Selection and Damage Mechanisms in Hydrogen Service

This course looks at the hydrogen technologies in the overall hydrogen life cycle from the point of its production through transportation and storage up to the point of consumption of the hydrogen, most notably as fuel for energy production.
ASME BPV Code, Section V: NDE Procedures and Personnel

This training course provides detailed insight into ASME Boiler and Pressure Vessel Code (BPVC) Section V, specifically focusing on Non-Destructive Examination (NDE) procedures and personnel qualifications.
Mechanical Seals

This comprehensive training course provides an in-depth introduction to mechanical seals, essential components critical for ensuring the reliability, safety, and efficiency of rotating equipment across diverse industrial sectors, including refining, petrochemical, power generation, and process industries.
Fracture Mechanics

Fracture mechanics is essential to maintaining the integrity, safety, and operational reliability of high-risk industrial assets.
Hydrogen Hazard Management & Safety Requirements for Production, Transport and Storage

The course provides deep insights in the safety relevant chemical and physical properties of hydrogen and the carrier molecules, which are used to store and transport hydrogen.
Quality & Regulatory Requirements for Drug Device Combination Products in the EU

This course will cover the definition of combination products, EU regulatory pathways, and will explain the current state of developments as medical device manufacturers and marketing authorisation holders prepare for the new requirements.
Advanced Damage Mechanisms and Materials Investigation

This training course will provide you with the adequate knowledge and skills to be well prepared and equipped to pass the API 571 Exam.
Bioassays & Bioanalytical Methods

This practical Bioassays and Bioanalytical Methods online live training is focused on complex therapeutics, such as Biopharmaceuticals, Biologics and Biosimilars.
Signal Management in Pharmacovigilance

This practical course provides an in-depth understanding of signal detection, signal validation & assessment as well as signal communication.
Relief & Flare Systems

The course covers relief, flare and vent systems design. It describes why specific equipment like separators and heat exchangers require relief protection and how to determine the relief cases for these items.
Control Valves & Actuated On/Off Valves

This practical course provides an in-depth understanding of polymorphic and multi-component systems.
Market Access for Digital Health Technology

This hands-on workshop is designed to provide practical, real-world experience in navigating the regulatory, reimbursement, and market access challenges for digital health apps.
Fiscal Metering & Custody Transfer

This three-day course provides an overview of the key aspects of a metering station designed for fiscal metering or custody transfer.
Computerized Systems Validation & Data Integrity in Pharma & Biotech Videorecording

This course is a compilation of topics representing recent challenges related to CSV, and how CSV relates to data integrity assurance.
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.