The course provides practical, hands-on experience in eCTD specifications, eSubmission requirements and data integrity for IDMP, SPOR and XEVMPD.
This advanced seminar is designed as an advanced course and will focus on all relevant topics for an expert in the field of medical scientific information. Our speakers will update you on all the applicable key issues.
This course will give you an in-depth knowledge on the CMC requirements for the marketing authorisation.
This international conference will take place on October 23 - 24, 2019. Stakeholders from every corner of the medical device world will meet in Amsterdam to discuss the latest trends and issues in regulatory affairs.
Do you need essential European regulatory affairs knowledge? This course gives you a compact overview about all important issues. Each day may be booked separately according to your needs!