FORUM Institut für Management courses

...How to establish a successful PV system for a product launch - How to handle the launch phases - PV due diligence - Typical challenges and how to handle...

...Emagister has recently added to its educational catalogue the Patient Access: Early Access, Compassionate Use, Off-label Use course endorsed by FORUM Institut für Management...

...Moreover, you will be familiar with the change management requirements to achieve regulatory and GMP compliance. - Day three will provide you with in-depth... Learn about: Change Management, Operational Risk, Operations Management...

...for IDMP and informs you on ePI (structured electronic product information) - a digitalisation project potentially utilizing IDMP and... Learn about: Online training, Medical Devices, Online Weiterbildung...

...Product approval - NMPA (CFDA): Documents, procedures, fees - tips and tricks - Clinical pathways - PMS (post-market surveillance) &... Learn about: Medical training, Change Management...

...Do you work in clinical trials? Then we would like to invite you to our live webcast in which experts from clinical research will inform you about... Learn about: Clinical Studies...

...No problem! Following each live meeting, you will be able to retrieve the recorded webcast (audio track and presentation) from our eLearning Centre... Learn about: Quality Training, Biological Chemistry, Biotechnology Engineering...

...two months with the latest regulatory and legislative developments. Thus, you will always have the essential information and trends in regulatory affairs...

...5 CTD - CMC data required for Module 3 (drug substance and drug product) - Dossier requirements for generics and further abridged procedures...

...This e-learning programme will familiarise you with the regulatory affairs principles outside the ICH region and show you how to categorise the various... Learn about: Marketing Communications, Marketing Processes, Marketing Tools...

...It addresses the EU marketing authorisation procedures for the various products. It will also introduce you to post-authorisation duties. - Upon completion... Learn about: Marketing Communications, Communication Training, Marketing Processes...

...Module 6: Other Post-Authorisation Procedures This e-Learning programme will provide you with detailed knowledge on the classification, grouping and submission...

...Efficient baseline creation - eCTD compilation and submission - Flexible time and place - Multiple-choice tests and personalised certificate... Learn about: Marketing Tools, Marketing Processes, Communication Training...

...of processes in the marketing authorisation phase as well as throughout the life cycle. - Legal basis for marketing authorisations - Dealing with deadlines... Learn about: Change Management, Operational Risk, Operations Management...

...This e-Learning programme will focus on stability testing for chemical and biological products in the ICH region. This e-Learning will provide you... Learn about: Marketing Processes, Marketing Communications, Marketing Tools...

...Module 3 is an essential part of the CTD. It presents data on the quality of the drug substance and drug product. But what data is required?...

...and major European players. - compliance rules you have to consider for your collaboration. - insights on how industry can effectively contact patient... Learn about: Marketing Tools, Marketing Communications, Communication Training...

...In this e-learning you will be introduced to backgrounds and the history of the blockchain technology. From this basis, it is much easier to grasp...

...achieving reasonable RoE when working with SME. - Become competent in different classical financing instruments, learn first aspects about 'Off-balancesheet financing'... Learn about: IT risk, Financial Training, Risk Analysis...

...Understand and make use of the appropriate tools when engaging or dismissing employees, or restructuring your business. - German key vocabulary is introduced... Learn about: Labour Law, Employment Law, IT Law...