Knowledge, Tools and Experience
are what separate the best from the rest.
Do it right and do it quickly.
Reliable, Innovative Regulatory Compliance Software
MedXview is the leading provider of regulatory compliance software solutions to the life science industry, including pharmaceutical companies, generic drug, and medical device manufacturers. Our software and service offerings ensure that your company complies with the latest regulations and policies and meets the strict standards of regulatory authorities all over the globe.
MedXview has the power to understand your document management and publishing needs. Trust our team of experts to help your company achieve quality, accuracy, and data integrity to deliver regulatory reports and submissions in a timely and efficient manner. You can either use our eSubmission software or have us submit the necessary documents for you to obtain FDA approval.
Our Key Capabilities
eCTD
We were one of the six software vendors at DIA eCTD showcase in 2004. We have been working on eCTD over 20 years.
SPL
Our SPL was one of the first five SPL labels that was listed on the FDA webpage in 2005.
eData
The CDISC board of directors for three years. SAS programming, data management, and submission data validation since 1998
eDMS
A reliable platform for online documents management, partnered with IBM since 2005.
Let’s Talk
Contact us today for more information about our regulatory submission software.
- Providing Services Worldwide
- Over 30 Years of Industry Experience
- In Business for More Than 24 Years
Contact us today to learn more about our software and outsourcing services.
Get in Touch
Address
50 California St., Suite 1500, San Francisco, CA 94111