Princeton, NJ - Please+Publish, a leading Document automation software, proudly announces the expansion of groundbreaking automation tools designed specifically for regulatory publishing, quality control (QC), and document formatting within the Life Sciences industry. This innovative suite of tools ensures regulatory compliance with industry standards while enhancing efficiency for companies by eliminating manual efforts.

"Our mission is to simplify the regulatory publishing process and ensure that our clients can focus on what matters most - the safe and effective development of pharmaceuticals," said Mahesh Malneedi. "With our advanced automation tools, organizations can significantly reduce the time and resources spent on document formatting and compliance checks, ultimately accelerating the path to market for new therapies."

Key features of Please+Publish's automation solutions:

• eCTD Compliance: Simplifies the preparation of electronic submissions to meet the global eCTD format.
• Automated QC: Reduces human error by automatically verifying documents for accuracy and consistency.
• Seamless Document Formatting: Ensures that all documents adhere to regulatory standards without manual intervention.

About Please+Publish

Please+Publish deploys advanced document processing technology to streamline regulatory publishing, quality control, and formatting tasks for small businesses and consultants. Recognizing the unique needs of smaller firms, we have tailored this tool to deliver the same level of efficiency as enterprise solutions, but in a simplified and cost-effective manner. Please+Publish platform is owned by DDi.

For more details, visit: https://www.pleasepublish.com/