12+
Years of experience
399
Events organized
3,710
Speakers
21,521
Attendees
Understand the values of PK/PD studies in drug R&D from an industrial perspective
learn more >>Scope of the ICH Guidelines Q6B for biotechnological products
learn more >>The use of PK during drug development will also be described.
learn more >>Ensure the adequate flow of any arising safety concerns!
learn more >>The risk benefit ratio should be maintained at all times
learn more >>The course covers general requirements for small molecules and biologics
learn more >>Manufacturing pharmaceuticals, especially biological products, is complex and expensive
learn more >>Unlock the keys to successful market access in the pharmaceutical industry
learn more >>The Entry Level CMC Masterclass covers the general requirements for small molecules and biologics.
learn more >>How to design and implement the systems your company needs.
learn more >>Principles, advantages and potential challenges of the adaptive design methodology
learn more >>Pharmacopoeias play a major role in quality standards for the manufacture and control of medicines in Europe and worldwide
learn more >>Are you planning to enter the EU or UK market to expand your market in the region?
learn more >>Microbiological contaminations can occur on many levels.
learn more >>Key elements for a successful development of a drug product analytical development
learn more >>This 2 days online masterclass gives practical examples from method validation and method transfer & pitfalls.
learn more >>This intensive online training will be held over 4 consecutive half-day sessions for lawyers, and paralegals, working in the pharmaceutical industry.
learn more >>Drafting the well structured, practical, clear and concise documents which achieve their objectives
learn more >>The MasterClass will cover aspects that are relevant for non-toxicologists involved in drug development
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 >>This online masterclass will address regulatory requirements related to cell bank establishment and testing.
learn more >>What the FDA is and how the entity is organized
learn more >>Interventional studies fall into the scope of Directive 2001/20/EC and will no be the object of this Masterclass.
learn more >>Guidance for conducting pesticide residue analysis, reviewing analytical results, or writing analytical reports
learn more >>Focus on topics and rules with a significant practical impact on routine residue analysis
learn more >>Learn more about identification and control of Leachables and Extractables
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!"