10+
Years of experience
299
Events organized
3,410
Speakers
17,761
Attendees
A series of practical exercises will take place throughout the programme to give participants the opportunity to apply their knowledge under the guidance of our experienced trainers.
learn more >>Interaction between pharmaceutical companies and patients/users through the Internet. Social media and two-way communication.
learn more >>Participants in this online masterclass will learn which trials in minors make sense, and which ones are pointless and even harmful.
learn more >>This comprehensive and detailed online masterclass describes the PK/PD studies from an industrial perspective to achieve a successful regulatory submission.
learn more >>The use of PK during drug development will also be described.
learn more >>This online training will present you what is meant by “Contamination Control Strategy”?
learn more >>This course will explain the current state of developments as medical device manufacturers and marketing authorisation holders prepare for the new requirements
learn more >>This course will train you in CRO oversight, and teach you how to design and implement the systems your company needs.
learn more >>The purpose of this Master Class is to introduce participants to the cornerstones of patient access and its value in context of CGT.
learn more >>This online masterclass will address regulatory requirements related to cell bank establishment and testing.
learn more >>This masterclass helps business leaders understand how to take action to manage nature related risks
learn more >>This training will explore the key aspects of the pharmacovigilance audits, from planning audit programmes, conducting audits to delivering audit findings through audit reports.
learn more >>The Entry Level CMC Masterclass covers the general requirements for small molecules and biologics.
learn more >>The training aims to generate a common understanding of how to best interlink two areas and create highly efficient processes.
learn more >>The training aims to generate a common understanding of how to best interlink two areas and create highly efficient processes.
learn more >>The Entry Level CMC Masterclass covers the general requirements for small molecules and biologics.
learn more >>The MasterClass will cover these aspects that are relevant for non-toxicologists involved in drug development
learn more >>In this training course you will learn how to deal with requirements of individual and general monographs and how to apply general chapters
learn more >>This online training will present you what is meant by “Contamination Control Strategy”?
learn more >>This online masterclass will address regulatory requirements related to cell bank establishment and testing.
learn more >>This Masterclass will train you in CRO oversight, and teach you how to design and implement the systems your company needs.
learn more >>This course gives a detailed expert overview of the questions and the topics of GMP audits
learn more >>This 1 day online masterclass gives practical examples from method validation and method transfer.
learn more >>This MasterClass will provide best understanding on how process validation for biotechnological products, which is the collection & evaluation of data from the process design stage.
learn more >>In this training course you will learn about the correct use of official (pharmacopoeial) standards and regulatory requirements.
learn more >>This 2 days online masterclass gives practical examples from method validation and method transfer & pitfalls.
learn more >>Are you planning to enter the EU market and/or expand your market in the region?
learn more >>Stability studies in relation to Biopharmaceuticals and Biosimilars
learn more >>Organic synthesis of major and minor cannabinoids and derivatives and their characterization will be presented.
learn more >>This is a very interactive online course with a lot of workshops, putting the theoretical concepts into practice.
learn more >>The environment for recombinant proteins used as biotherapeutics is changing.
learn more >>This course gives a detailed expert overview of the questions and the topics of GMP audits
learn more >>The focus of this two days pharma online masterclass will be on providing an update of ongoing activities regarding medicines’ risk and signal management.
learn more >>Advanced e-PIL & E-Leaflet MasterClass provide the attendee with the building blocks for the establishment and delivery of an e-PIL strategic initiative identifying where the organisation most significantly impacted.
learn more >>This MasterClass will provide best understanding on how process validation for biotechnological processes.
learn more >>Years of experience
Events organized
Speakers
Attendees
"High attention to detail in course content and very well delivered"
"Very good training led by two knowledgeable and open experts. Excellent insight given on many complex topics. Interactive and highly useful"
"Great course, impressed with the knowledge of the trainers and ability to answer wide variety of questions!"