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Gain invaluable insights into the development, regulation, and deployment of AI-powered medical devices

The route to Strategic Business Advantage

The focus becomes strategic risk management

Pharmaceutical companies and patients/users interact through theInternet,Social media,and two-way communication.

Pharmaceutical companies and patients/users interact through theInternet,Social media,and two-way communication.

Understand how to qualify scale-down models

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

This masterclass helps business leaders understand how to take action to manage nature related risks

Knowledge of Basel and its EU form

Understand the Paris Agreement and Net Zero Goals

Understand the Paris Agreement and Net Zero Goals

From regulatory compliance to technical innovation, from financial scrutiny to operational efficiency

Current developments for impurities in small molecule APIs and respective medicinal products

QbD concept, process validation, and regulatory requirements!

A comprehensive overview of the BCBS framework on IRRBB and implementation

A comprehensive overview of the BCBS framework on IRRBB and implementation

How to design and implement the systems your company needs.

The latest revision to ICH GCP

Cutting edge methodologies, regulations and principles in driving sustainable change

Implementation of Quality by Design principles.

Implementation of Quality by Design principles.

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

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

Key points for successful development and registration of products in US

Development and validation of bioassays

Development and validation of bioassays

Beyond Child's Play

Beyond Child's Play

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.

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.

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

Biologics, Biopharmaceuticals, Biosimilars & ATMPs

A phenomena for complex therapeutics

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)

Aseptic Filling of Biologics & Finish

Aseptic Filling of Biologics & Finish

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

The biggest HR Conference in the Europe

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

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.

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.