Pharma

Signal and Risk Management in Pharmacovigilance US MasterClass

Signal and Risk Management in Pharmacovigilance US MasterClass

23 - 26 May, 2022

The focus of this two days pharma online masterclass will be on providing an update of ongoing activities regarding medicines’ risk and signal management.

CRO Oversight MasterClass

CRO Oversight MasterClass

26 & 27 May, 2022

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

Viral Clearance MasterClass

Viral Clearance MasterClass

30 & 31 May, 2022

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

Advanced CMC MasterClass

Advanced CMC MasterClass

13 & 14 June, 2022

This online masterclass will go through the key scientific points for the development and registration of your medicine.

Decentralized Clinical Trials MasterClass

Decentralized Clinical Trials MasterClass

21 & 22 June, 2022

This online masterclass will provide an overview in regards to the planning and conduction of Decentralized Clinical Trials for sponsors, Contract Reasearch Organizations and site.

Process Validation for Biotechnological Products MasterClass

Process Validation for Biotechnological Products MasterClass

20 - 23 June, 2022

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.

Contamination Control Strategy MasterClass

Contamination Control Strategy MasterClass

27 & 28 June, 2022

 This online training will present you what is meant by “Contamination Control Strategy”?

Advanced Quality Risk Management MasterClass

Advanced Quality Risk Management MasterClass

13 & 14 July, 2022

This Masterclass will provide you to gain insight into how quality risk management (QRM) can be integrated into a modern pharmaceutical quality management system.

Deviation and Change Control Management in Pharma MasterClass

Deviation and Change Control Management in Pharma MasterClass

01 & 02 September, 2022

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

Pharmacovigilance System Master File MasterClass

Pharmacovigilance System Master File MasterClass

05 - 06 September, 2022

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

Pediatric Drug Development MasterClass

Pediatric Drug Development MasterClass

05 - 07 September, 2022

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 Asian MasterClass

Advanced Stability Testing of Pharmaceuticals Asian MasterClass

05 - 08 September, 2022

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

Pharma M&A MasterClass

Pharma M&A MasterClass

06 - 09 September, 2022

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

CRO Oversight MasterClass

CRO Oversight MasterClass

07 & 08 September, 2022

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

Method Validation and Transfer with focus on the new ICH Q2(R2) MasterClass

Method Validation and Transfer with focus on the new ICH Q2(R2) MasterClass

12 September, 2022

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

PK/PD in Drug Discovery and Development for the US market MasterClass

PK/PD in Drug Discovery and Development for the US market MasterClass

12 - 15 September, 2022

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

Pharmacovigilance Audit and Inspections US MasterClass

Pharmacovigilance Audit and Inspections US MasterClass

13 - 15 September, 2022

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

Pharma M&A MasterClass

Pharma M&A MasterClass

19 - 20 September, 2022

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

Behavioural Good Manufacturing Practices MasterClass

Behavioural Good Manufacturing Practices MasterClass

19 & 20 September, 2022

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

Clinical Project Management MasterClass

Clinical Project Management MasterClass

26 - 29 September, 2022

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

Leading a Strategic Account Management Approach in Pharma MasterClass

Leading a Strategic Account Management Approach in Pharma MasterClass

27 - 28 September, 2022

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

Viral Clearance MasterClass

Viral Clearance MasterClass

03 - 04 October, 2022

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

Vaccine Development MasterClass

Vaccine Development MasterClass

03 - 05 October, 2022

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

Process Validation for Biotechnological Products Asian MasterClass

Process Validation for Biotechnological Products Asian MasterClass

18 - 21 October, 2022

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.

10+

Years of experience

299

Events organized

3,410

Speakers

17,761

Attendees

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Testimonial

Our success stories

"High attention to detail in course content and very well delivered"

Simon Halsey
Product Development Manager
Essentra Packaging
United Kingdom

Our success stories

"Very good training led by two knowledgeable and open experts. Excellent insight given on many complex topics. Interactive and highly useful"

Aurelie Vivicorsi
USP PD Team Manager
Celonic AG
Switzerland

Our success stories

"Great course, impressed with the knowledge of the trainers and ability to answer wide variety of questions!"

Emilia Szwej
Manager, Senior Investigator
MT Sword Laboratories (BMS)
Germany