January 2026 marks the start of a new reporting era under the amended Common Reporting Standard (CRS). The OECD released the CRS XML Schema v3.0 ...
The Study Data Reviewer’s Guide (SDRG) helps reviewers process clinical trial data more efficiently. According to the FDA’s ...
Creating an invoice in Site.pro is straightforward and begins in the Sales module. Open the Sales section and select “ Create invoice ”. The system automatically populates basic fields such as the ...
Split your metadata from your files, and suddenly your sluggish document system becomes fast, scalable and surprisingly cheap to run.
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