FORUM Institut für Management courses

...them Why should pharmacovigilance be involved in product launches or licencing transfers? This online-seminar will provide the answers...

...off-label use and hospital exemption This online seminar provides information on early access programmes, HTA requirements, CUP and off-label use in Europe...

...Kazakhstan and Belarus This online seminar provides you within-depth knowledge on marketing authorisation, CMC documents and GMP-requirements in Russia... Learn about: Change Management, Operations Management, Operational Risk...

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

...novelties in China entail and which are significant for you as an European medical device manufacturer. Questions and discussions are explicitly welcome... Learn about: Medical training, Change Management...

...you every month with the latest updates and trends in clinical studies. Thus, you will always have essential information on the design and conduct of clinical trials... 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, Biotechnology Engineering, Biological Chemistry...

...Following each live meeting, you will be able to retrieve the recorded webcast (audio track and presentation) from our eLearning Centre, using your personal password...

...This e-Learning programme will provide you with detailed knowledge on the structure and content of the (electronic) common technical document...

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

...This e-Learning programme will provide you with detailed knowledge on the classification, grouping and submission of variations in the EU. It includes...

...in the course of the 'eCTD in the Middle East' live webcast series in April 2019. - Screening and editing essential marketing authorisation documents... Learn about: Marketing Tools, Communication Training, Marketing Processes...

...conditions, etc. - Orphan drugs and paediatric development - Preparing for referrals - Contracts in regulatory affairs - IP and generics development These... Learn about: Operational Risk, Operations Management, Change Management...

...knowledge of regulatory frameworks in Europe, the ICH region and the US; - an understanding of the chemical, physical and microbiological factors influencing stability testing... Learn about: Communication Training, Marketing Processes, Marketing Tools...

...CTD structure and applicable guidelines - Drug substance Part - ASMF and CEP - Drug product part This e-Learning programme will familiarise you with...

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

...its applications like smart contracts and especially, its limits. So after this e-learning you will be able to - explain what a smart contract...

...The introductory training course will inform you according to which criteria SMEs in Germany are segmented and defined. You will get an understanding about general aspects... Learn about: Financial Training, IT risk, Risk Analysis...

...remuneration and bonus payments, minimum salary... Learn about: Employment Law, IT Law, Labour Law...