eSTAR Office Hours

Free consultancy on how to adapt to the mandatory eSTAR submission process.

  • Video call with our eSTAR experts

  • Zero cost (we are happy to support the RA community on this challenging transition)

eSTAR Office Hours

30-min of free consultancy on how to adapt to the mandatory eSTAR submission process

Essenvia Customer for 3+ Years

“

Essenvia greatly shortens the time to submission. It saved us countless hours in managing files, edits, and even major updates at the last minute for very complex submissions. We can’t live without the platform”

Essenvia greatly shortens the time to submission. It saved us countless hours in managing files, edits, and even major updates at the last minute for very complex submissions. We can’t live without the platform”

John Landsdown

GM - Quality, Regulatory and Compliance

Essenvia Customer for 2+ Years

“

With the help of the Essenvia Platform, we have successfully obtained clearance both in the UK and in the EU! Essenvia has truly been instrumental in our success, and we are grateful for your continued support”

With the help of the Essenvia Platform, we have successfully obtained clearance both in the UK and in the EU! Essenvia has truly been instrumental in our success, and we are grateful for your continued support”

VP of Clinical, Regulatory, and Quality Affairs

A global publicly traded In Vitro Diagnostics company

Navigate the complex world of regulatory compliance with confidence.

Get a Free Demo Today

Get a Free Demo Today

Get a Free Demo Today

Get a Free Demo Today

Essenvia Customer for 3+ Years

“

We completed and successfully submitted our first FDA eSTAR submission using Essenvia.  Thanks to Essenvia our team was able to work together in one single place at any time to author, edit, and review the submission. As a regulatory leader, I also love seeing the total progress of the submission and individual sections as it’s being prepared and completed”

We completed and successfully submitted our first FDA eSTAR submission using Essenvia.  Thanks to Essenvia our team was able to work together in one single place at any time to author, edit, and review the submission. As a regulatory leader, I also love seeing the total progress of the submission and individual sections as it’s being prepared and completed”

Marta Stepien

VP of Clinical, Regulatory and Quality Affairs

Essenvia Customer for 2+ Years

“

Essenvia's PMA automation tool has revolutionized our regulatory affairs operations. By streamlining administrative tasks and enhancing data visibility, we saved time and improved accuracy. The eSTAR and RIM systems ensure 100% submission accuracy and project tracking, while the submission edit features expedite processes and facilitate collaboration. They provided exceptional customer service, and the Essenvia technology exceeded our expectations, proving to bean invaluable asset to our company”

Essenvia's PMA automation tool has revolutionized our regulatory affairs operations. By streamlining administrative tasks and enhancing data visibility, we saved time and improved accuracy. The eSTAR and RIM systems ensure 100% submission accuracy and project tracking, while the submission edit features expedite processes and facilitate collaboration. They provided exceptional customer service, and the Essenvia technology exceeded our expectations, proving to bean invaluable asset to our company”

VP of Clinical and Regulatory Affairs

A global leader in the preservation and perfusion of organs

Accelerate global market access, reduce costs, and focus on what your company does best: Innovation!

Get a Free Demo Today

Get a Free Demo Today

Get a Free Demo Today

Get a Free Demo Today