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Design stability studies for global marketing

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

Unlock the keys to successful market access in the pharmaceutical industry

The latest revision to ICH GCP

The concept of authentic leadership can help in overcoming difficulties in professional relationship building

The route to Strategic Business Advantage

Adoption of New Critical to Quality Requirements

Learn more about identification and control of Leachables and Extractables

Understand how to qualify scale-down models

Pharmacokinetics (PK) play a key role in drug development

Increase the likelihood of studies receiving regulatory approval

A comprehensive overview of the BCBS framework on IRRBB and implementation

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

Knowledge of Basel and its EU form

Scope of the ICH Guidelines Q6B for biotechnological products

The use of PK during drug development will also be described.

Ensure the adequate flow of any arising safety concerns!

The risk benefit ratio should be maintained at all times

 The course covers general requirements for small molecules and biologics

 Manufacturing pharmaceuticals, especially biological products, is complex and expensive

Unlock the keys to successful market access in the pharmaceutical industry

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

Including EU's latest on PSD3, PSR, FIDA

How to design and implement the systems your company needs.

In some minds, mentioning Securitisation raises the spectre of the global financial crisis precipitated by the mis-rating of and huge losses

How would you know if fraud was occurring in your organisation?

How would you know if fraud was occurring in your organisation?

Principles, advantages and potential challenges of the adaptive design methodology

Pharmacopoeias play a major role in quality standards for the manufacture and control of medicines in Europe and worldwide

Are you planning to enter the EU or UK market to expand your market in the region?

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

This intensive online training will be held over 4 consecutive half-day sessions for lawyers, and paralegals, working in the pharmaceutical industry.

 The MasterClass will cover aspects that are relevant for non-toxicologists involved in drug development

 Structured products are now used by professional investors, advisors and asset managers worldwide

A theoretical and practical understanding of stress testing methodology

Working knowledge of blockchain and understanding of strategic implications

Master the Time Management skill

Master the Time Management skill

 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?

Join our 9th Annual Internal Audit Forum to network and exchange information with experts from all across the world.

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

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.