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Signal and Risk Management in Pharmacovigilance MasterClass

Signal and Risk Management in Pharmacovigilance MasterClass

09 & 10 December, 2021

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

The EU Clinical Trial Regulation MasterClass

The EU Clinical Trial Regulation MasterClass

16 & 17 December, 2021

This Online MasterClass will provide an essential understanding to help with compliance with the new EU Clinical Trial Regulation (536/2014) and associated implementing acts for carrying out clinical trials in the EU.

Vendor/CRO Management and Oversight MasterClass

Vendor/CRO Management and Oversight MasterClass

12 & 13 January, 2022

On this MasterClass Training you will learn how to prepare a request for proposal (RFP), evaluate and select the right CRO and establish procedures for vendor oversight for projects you need to outsource.

Process Validation for Biotechnological Products MasterClass

Process Validation for Biotechnological Products MasterClass

17 - 20 January, 2022

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

Vendor/CRO Management and Oversight MasterClass

Vendor/CRO Management and Oversight MasterClass

19 & 20 January, 2022

On this MasterClass Training you will learn how to prepare a request for proposal (RFP), evaluate and select the right CRO and establish procedures for vendor oversight for projects you need to outsource.

Regulated LC-MS Bioanalysis Masterclass

Regulated LC-MS Bioanalysis Masterclass

26 & 27 January, 2022

This training is intended for professionals who work in the field of analytical chemistry, focusing on HPLC, UHPLC and LC-MS. This training will provide effective method development, sample analysis and comprehensive troubleshooting.

Advanced Stability Testing of Pharmaceuticals MasterClass

Advanced Stability Testing of Pharmaceuticals MasterClass

01 - 04 February, 2022

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

Advanced E-PPI and E-Leaflet US MasterClass

Advanced E-PPI and E-Leaflet US MasterClass

07 & 08 February, 2022

This Training will provide Key Points for the Establishment, Development and Implementation of E-PPI strategy and E-Leaflets.

Advanced CMC MasterClass

Advanced CMC MasterClass

07 - 08 - 09 February, 2022

 This training will present key points in CMC which are currently the focus of Health Authorities + 1 Day training on How to submit variations in Europe.

Leading a Strategic Account Management Approach in Pharma MasterClass

Leading a Strategic Account Management Approach in Pharma MasterClass

08 - 09 February, 2022

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

Process Validation for Biotechnological Products MasterClass

Process Validation for Biotechnological Products MasterClass

14 - 17 February, 2022

This 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.

The Future of Internal Audit MasterClass

The Future of Internal Audit MasterClass

10 & 11 February, 2022

The Internal Audit Online MasterClass Provides a Best Opportunity to Develop new Approaches to the Difficult Challenges Facing Modern Audit Functions.

CCR and CCP Risk Management MasterClass

CCR and CCP Risk Management MasterClass

21 & 22 February, 2022

This training is intended to provide an appreciation of central counterparty clearing particularly in relation to the clearing of OTC derivatives.

Pharmacovigilance Audit and Inspections MasterClass

Pharmacovigilance Audit and Inspections MasterClass

22 - 24 February, 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 Analysing and Drafting Commercial Contracts MasterClass

Pharma Analysing and Drafting Commercial Contracts MasterClass

22 - 25 February, 2022

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

Alternate Approaches to Validating a Computer System MasterClass

Alternate Approaches to Validating a Computer System MasterClass

28 February - 01 March, 2022

This MasterClass will take a deep dive into the mechanics, documentation, and compliance requirements for completing a validation effort.

US Pharma Contract Drafting MasterClass

US Pharma Contract Drafting MasterClass

28 February - 03 March, 2022

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

Critical Quality Attributes of Recombinant Proteins for Therapeutic Use MasterClass

Critical Quality Attributes of Recombinant Proteins for Therapeutic Use MasterClass

07 & 08 March, 2022

Critical quality attributes of recombinant proteins for therapeutic use Masterclass will address the understanding of quality attributes, the purpose of assessing their criticality and how to select critical quality attributes.

CRO Contracting and Oversight MasterClass

CRO Contracting and Oversight MasterClass

07 & 08 March, 2022

This Masterclass will train you in CRO oversight, and teach you how to design and implement the systems your company needs.

Regulatory and Technology Considerations for the Design of Medical Device Software MasterClass

Regulatory and Technology Considerations for the Design of Medical Device Software MasterClass

07 - 09 March, 2022

This MasterClass Will Cover Medical Device Classification and Regulatory Requirements and also Participants will understand Implication of lifecycle management.

EU Clinical Trial Regulation MasterClass

EU Clinical Trial Regulation MasterClass

07 - 09 March, 2022

This Masterclass will provide the attendees with an understanding of the new processes and requirements for EU sponsors of clinical trials as the new regulation is published.

Advanced CMC MasterClass

Advanced CMC MasterClass

09 & 10 March, 2022

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

LifeSciences | Making Print Personal MasterClass

LifeSciences | Making Print Personal MasterClass

21 & 22 March, 2022

This Masterclass will explore how the adoption of Digital capabilities, specifically the Inkjet Drop on Demand (DOD) technology can generate benefit and opportunity.

Advanced Stability Testing of Pharmaceuticals MasterClass

Advanced Stability Testing of Pharmaceuticals MasterClass

21 - 24 March, 2022

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

Agile Audit and Assurance MasterClass

Agile Audit and Assurance MasterClass

22 - 24 March, 2022

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

Safety Data Exchange Agreements (SDEAs) and PV Arrangements with External Vendors MasterClass

Safety Data Exchange Agreements (SDEAs) and PV Arrangements with External Vendors MasterClass

23 & 24 March, 2022

This Online MasterClass Provides How to assure that all safety information is captured and collected in the Safety Databases.

Advanced Quality Assurance MasterClass

Advanced Quality Assurance MasterClass

28 & 29 March, 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.

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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