13+
Years of experience
500+
Events organized
3,970
Speakers
23,714
Attendees
From regulatory compliance to technical innovation, from financial scrutiny to operational efficiency
learn more >>Current developments for impurities in small molecule APIs and respective medicinal products
learn more >>QbD concept, process validation, and regulatory requirements!
learn more >>How to design and implement the systems your company needs.
learn more >>The latest revision to ICH GCP
learn more >>Implementation of Quality by Design principles.
learn more >>Implementation of Quality by Design principles.
learn more >>Key elements for a successful development of a drug product analytical development
learn more >>This online masterclass gives practical examples from method validation and method transfer.
learn more >>Key points for successful development and registration of products in US
learn more >>Development and validation of bioassays
learn more >>Development and validation of bioassays
learn more >>Beyond Child's Play
learn more >>Beyond Child's Play
learn more >>The Entry Level CMC Masterclass covers the general requirements for small molecules and biologics.
learn more >>Paving the Way from Development to Lifecycle Management
learn more >>The training aims to generate a common understanding of how to best interlink two areas and create highly efficient processes.
learn more >>A comprehensive overlook on benefit risk assessment in PSUR and RMP
learn more >>Connection between risk management with PBRERs and benefit-risk assessment and tools
learn more >>Mastering Dissolution Testing: From Basics to Advanced Techniques
learn more >>Managing CMOs with condence, insight and understanding
learn more >>Biologics, Biopharmaceuticals, Biosimilars & ATMPs
learn more >>A phenomena for complex therapeutics
learn more >>International experiences
learn more >>The EU Medical Device Regulation (MDR)
learn more >>This online masterclass will address regulatory requirements related to cell bank establishment and testing.
learn more >>The Master Cell Bank is not only the starting point of GMPs but also the starting point of the therapeutical recombinant proteins and GTP
learn more >>RBQM principles that align with regulatory expectations
learn more >>RBQM principles that align with regulatory expectations
learn more >>Aseptic Filling of Biologics & Finish
learn more >>Aseptic Filling of Biologics & Finish
learn more >>Key elements for a successful development of a drug product analytical development
learn more >>Pharmacokinetics (PK) play a key role in drug development
learn more >>Drug Interaction studies!
learn more >>Optimizing drug development and translational medicine strategies
learn more >>Understand the values of PK/PD studies in drug R&D from an industrial perspective
learn more >>Today, process validation comprises three main steps:
learn more >>Key points for successful development and registration of your pharmaceutical products
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!"