Pharma

In this online masterclass course you will not only learn about the theory, but for each topic examples from practice will also be shown.

This MasterClass shall describe the pharmacovigilance system and support/document its compliance with the requirements.

Participants in this online masterclass will learn which trials in minors make sense, and which ones are pointless and even harmful.

Advanced Stability Testing of Pharmaceuticals MasterClass will cover the scientific principles of chemical & physico-chemical degradation of active substances & pharmaceutical products.

This specialized online training event will address the particular issues which affect Pharmaceutical M&A work.

CRO Oversight online masterclass provides an overview of the key concepts and best practices for CRO management in a global clinical trial setting.

This Masterclass will sensitize participants for the value patient engagement and provide a brief introduction.

This 1 day online masterclass gives practical examples from method validation and method transfer.

This comprehensive and detailed online masterclass describes the PK/PD studies from an industrial perspective to achieve a successful regulatory submission.

This training will explore the key aspects of the pharmacovigilance audits, from planning audit programmes, conducting audits to delivering audit findings through audit reports.

This Masterclass is intensive, and aimed at participants who wish to understand the various legal aspects of M&A in its different facets.

This Masterclass will ensure that value added changes in compliance are achieved and more importantly sustained.

Advanced Stability Testing of Pharmaceuticals MasterClass will cover the scientific principles of chemical & physico-chemical degradation of active substances & pharmaceutical products.

The training aims to provide deeper understanding on how process validation for biotechnological processes, which is the collection and evaluation of data from the process design stage through commercial production.

This is a very interactive online course with a lot of workshops, putting the theoretical concepts into practice.

This 2 days online masterclass gives practical examples from method validation and method transfer & pitfalls.

Viral Clearance online masterclass will give an overview of the sources and impacts of viral contaminations of biotherapeutics.

This online masterclass guides through the technical, scientific & political paradigm shifts of vaccine development.

 This training will present Technical and regulatory requirements for developing a medicinal product which are becoming stricter every day, the products themselves become more and more complex.

This MasterClass shall describe the general increase in combination products and in particular products now regulated by both drug and medical device regulation.

This public training course will cover the scientific principles of chemical and physico-chemical degradation of active substances and pharmaceutical products.

The Online training Course's goal to cover the technical and organisational requirements and procedures of pharma and healthcare packaging and technical operations in a 360-degree coverage.

The focus of this online training is on the ICH guideline Q6B.

This Online MasterClass will provide best understanding on how process validation for biotechnological products, which is the collection and evaluation of data from the process design stage through commercial production.

This 1 day online masterclass gives practical examples from method validation and method transfer. The new draft ICH guideline for method validation ICHQ2(R2) has been published for comment.

This Online Training will provide how to develop and lead your organisational SAM/KAM strategy and through best practice tools and techniques.

This online masterclass will address regulatory requirements related to cell bank establishment and testing.