Check events

A comprehensive overlook on benefit risk assessment in PSUR and RMP

Connection between risk management with PBRERs and benefit-risk assessment and tools

Mastering Dissolution Testing: From Basics to Advanced Techniques

Managing CMOs with condence, insight and understanding

The Entry Level CMC Masterclass covers the general requirements for small molecules and biologics.

Develop new Approaches to the Difficult Challenges Facing Modern Audit Functions.

Biologics, Biopharmaceuticals, Biosimilars & ATMPs

A phenomena for complex therapeutics

Paving the Way from Development to Lifecycle Management

The training aims to generate a common understanding of how to best interlink two areas and create highly efficient processes.

International experiences

Integrating business concepts from the best-selling book The Great Game of Business

Integrating business concepts from the best-selling book The Great Game of Business

The EU Medical Device Regulation (MDR)

Why Attend Basel 4 Training on Credit Risk?

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

The Master Cell Bank is not only the starting point of GMPs but also the starting point of the therapeutical recombinant proteins and GTP

Aarons CLEAN Framework for chemical distribution

Five fundamental steps!

RBQM principles that align with regulatory expectations

RBQM principles that align with regulatory expectations

Aseptic Filling of Biologics & Finish

Aseptic Filling of Biologics & Finish

Key elements for a successful development of a drug product analytical development

Pharmacokinetics (PK) play a key role in drug development

Drug Interaction studies!

Optimizing drug development and translational medicine strategies

Understand the values of PK/PD studies in drug R&D from an industrial perspective

The latest revision to ICH GCP

Design stability studies for global marketing

Increase the likelihood of studies receiving regulatory approval

Global Medical Device regulations

Inspection readiness

Establishing, Maintaining and Demonstrating Sponsor Oversight

Regulatory requirements, sources, responsibilities, characterisation, management, and use

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

Join us in Budapest, on the 19th and 20th of February and be part of pharmaceutical packaging and labellings future!

Join our 10th Annual Internal Audit Forum to network and exchange information with experts from all across the world.

The biggest HR Conference in the Europe

Optimization of drug development and translational medicine strategies from pre-clinical to clinical proof-of-concept.

Pharmacokinetics (PK) play a key role in drug development

Key elements for a successful development of a drug product analytical development

This in-house training will inform about quality testing procedures of packaging materials such as AQL testing in packaging controls and reduced sampling procedures.

What are the key components of communication?

What are the key components of communication?

HSE360 will provide participants with a platform for information exchange and networking with experts from all across the world.

Key points for successful development and registration of products in US

Today, process validation comprises three main steps:

Key points for successful development and registration of your pharmaceutical products

NIS is helpful to obtain information forming hypotheses for new research projects.

QP`s role in clinical project setup will highlight the key points for quality and the qualified person (QP) to consider when setting up clinical trial.

This in-house training will give practical examples from method validation and method transfer & pitfalls. Also Participants can ask questions interactively.

This in-house training will address potential issues encountered when establishing cell banks and will discuss operational aspects for ensuring good quality cell banks. 

This In-house training provides deeper understanding on how process validation for biotechnological processes.

This in-house 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 In-house training will provide participants with an overview of approaches to forecasting ranging from the classical linearforecasting methods to non-linear approaches.

This In-house training covers the theory & practice of Blockchains/Distributed Ledger Technology. It provides far more than just an understanding of the technology. 

Blockchain for Pharma is an ideal candidate to address issued across supply chain, clinical trials and R&D.

This In-house training considers some of the tactics that could be used to hedge the associated market and credit risk of a fixed income portfolio.

The aim of this In-house training is to provide all those involved with IVDs a broad overview of the IVDR with practical guidance.

This In-house training will support you in collecting, sorting and proper understanding of the requirements of the serialisation Requirements.

This in-house training will provide an introduction to the Agile methodology and Outline the areas of focus for the audit and assurance review of Agile project.