NNIT’s Regulatory Affairs Intelligence Service provides Life Science company with all the relevant information and regulations from international conferences and EMA and FDA meetings – allowing you to stay updated and compliant in a more efficient way.
It is paramount for life science organizations to stay updated on regulatory affairs transformation – but it is also costly and time-consuming. To help companies navigate the increasingly complex and fast changing regulatory affairs and related IT systems, NNIT has developed the RA Intelligence Service.
On behalf of our clients, NNIT’s experts join international Regulatory Affairs conferences as well as EMA and FDA meetings and bring back the most relevant information and newest best practices. Following the event, the experts produce a meeting digest and present the conference take-aways at a live webinar. The presentation and a detailed summary of the event will be sent to you less than a week after the webinar.
NNIT’s experts have in-depth knowledge in areas such as XEVMPD, IDMP, RA systems (RIMS, EDMS) and RA regulations from EMA and FDA.
You stay updated using fewer resources. You do not need to spend valuable time and budgets on attending international conferences but can still keep your business updated on RA IT Regulation.
You gain insight into the most relevant regulations. NNIT’s experts will guide you through the most relevant information at the webinar. They will transform the new knowledge into practice for your company’s Regulatory Affairs team.
The participation fee is EUR 335 (DKK 2,500) per session you join. The price stated is per company with no limits on the number of employees taking part in the webinar.
You can indicate in advance whether you are interested in the conference, but only pay when and if you want to participate in the webinar.
Article written: June 2018