Veeva Solutions
Get a strong start with Veeva RIM Suite

- Rowan Nidd, Advisory Director, Regulatory Affairs, NNIT
Veeva RIM is excellent for managing regulatory documents, drug submissions and registrations. And the right partner can help you ensure that everything runs smoothly from the start.
Get the terminology right from the start
– Many of the terms used by Veeva are similar to those used in a typical pharma company, but in some cases they can mean different things. That is why you should choose an implementation partner with in-depth knowledge of both Veeva RIM and pharma business processes, Rowan Nidd, Advisory Director, Regulatory Affairs at NNIT, explains.
Plan for regulatory changes
This is an area where a partner like NNIT can provide guidance and ask all the right questions, also after go-live.
Valuable lessons about Veeva RIM
Among other things, our vast experience with Veeva RIM has taught us that it is important to:
Consider starting small: For organizations with limited resources, starting out with specific products like Submissions or Registrations may be better than trying to implement the entire Veeva RIM all at once. Begin by identifying the areas where migrating to Veeva provides the most value and use standard templates and best practices to keep configuration efforts to a minimum.
Replace documents with data: With Veeva RIM, you are able to work at data level, meaning that you can send data packages instead of producing pdf documents. This enables greater use of automation and machine-to-machine communication.
Prioritize change management: Training and organizational change management are essential – and often overlooked – prerequisites for success with Veeva RIM.
Get a trusted partner: Maximizing the value you gain from Veeva RIM requires continuous work and a long-term focus. This is much easier to achieve with the assistance of an experienced partner that can apply both life sciences insights and hands-on Veeva experience.
Where are you on the journey to Veeva operational maturity?
