Prepare for IDMP with the #1 Solution in Readiness

Are you confident your regulatory systems will be able to standardize the data to be IDMP compliant? Will you be able to test in advance of the EU deadline? 

With LifeSphere IDMP, you can be assured that you will remain compliant throughout the regulatory lifecycle. 



Go Beyond IDMP Compliance

IDMP data standards are forcing companies to capture more data than ever before — and effective data management can be time-consuming and costly. Get ahead of changing regulations and timelines with the right technology and processes in place.

Prepare today, save time (and stress) tomorrow

We have reimagined and enhanced our solution with future standardization in mind, and are a leader in IDMP according to Gens and Associates.

As ISO countries adapt and adopt their versions of IDMP, we will be ready to implement their requirements ensuring that you remain compliant, saving you time, money, and stress. 

Built with Industry

LifeSphere IDMP was developed in partnership with top life sciences organizations. Our partnerships and adherence to Regulatory best practices will continue to inform our development.

Secure Open Architecture

Through Open Architecture LifeSphere IDMP allows for seamless integration throughout your organization, maintaining data integrity and ensuring IDMP compliance across the drug development lifecycle. 

Implementation Available Now

Implement LifeSphere IDMP today so you can test in advance of the approaching EU deadline. 

Future Proofed Compliance

LifeSphere Regulatory was designed to accommodate IDMP in EU along with all future iterations of IDMP and other standards. 

LifeSphere IDMP is designed to help Eisai stay in step with changing regulations with ease and reduce the burden on Regulatory teams.

Below is curated content on how ArisGlobal can help Eisai prepare for IDMP and future regulations compliance.

IDMP Readiness Checklist: A Guide to Preparing for the New ISO Standard.

With IDMP, every aspect of your organization will be affected: from discovery to post-market authorization, all referentials will need to be uniform. 

To Prepare for IDMP, Organizations Must Think Years Ahead – Not Months.

IDMP is fast approaching, but life science organizations would be wise to vet long-term solutions over quick-fix stopgaps.

Leveraging IDMP Across All Business Functions to Proactively Manage Global Regulatory Affairs.
Remaining compliant is increasignly difficult, and as ISO countries finalize IDMP standards, many organizations are taking a pause to see if they are ready to remain compliant.