Veeva eTMF

Electronic Trial Master Files management is one of the important tasks in clinical trials. Integrity of these files is critical for regulatory submissions. Veeva’s eTMF solution enables trial master files management streamlined. Companies can maintain all files related to all studies across all CRO’s and sites in one centralized location. This provides better control and compliance that is more efficient in accessing status, content or reports.

We help with strategy, scoping, business process and workflow definition, ensuring functional needs are aligned with Veeva and configurations are in line with business need. We create required compliance, system and training documentation that is user centric. We help with testing, validation, data migration, integration, training and post implementation support.

Don’t worry about sounding professional. Sound like you. There are over 1.5 billion websites out there, but your story is what’s going to separate this one from the rest. If you read the words back and don’t hear your own voice in your head, that’s a good sign you still have more work to do.

Be clear, be confident and don’t overthink it. The beauty of your story is that it’s going to continue to evolve and your site can evolve with it. Your goal should be to make it feel right for right now. Later will take care of itself. It always does.