This 3-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.
Understand the specific regulatory & legal environment concerning generic medicinal products. Update your knowledge on regulatory procedures for new applications and variations. Get an overview of the documentation for Generic applications. Understand the current integrated life-cycle approach from development to registration and maintenance, including ICH Q12.
Take advantage of this unique product that combines classroom training and online learning with the aim of maximizing the implementation of the information learned.
This 3-day master-class seminar will cover in-depth on the topic of well plugging and abandonment, an essential step of the decommissioning phase when well integrity must be assessed, repaired – if needed – and assured for a long time into the future.
In-depth look at the EU GDP Guidelines and their application in areas of transport. Topics covered during the training will highlight deficiencies identified during regulatory inspections of wholesale distributors involved in the transport of temperature sensitive medicinal products. This will include ambient medicinal products as they are also temperature sensitive products.