Wednesday, 20 October 2021You want to make sure that Microsoft Word & PDF documents meet compliance guidelines. And that they are fixed automatically if they don’t. By watching the recording, you learn more about:
How to auto check and fix Word and PDF documents for compliance Read More »
21 April 2022, Thursday, between 17:00 – 17:30 CETRegulatory submissions are one of the most critical milestones for Life Sciences organizations and can consist of thousands of documents. Submitting on time and in full compliance with Regulatory Agencies’ requirements remains a challenge for many companies. Today, many Life Sciences companies still struggle with their submission
June 9, 2022 (Thursday) 17:00 -17:30 PM CETAre you creating your reports manually today? Or perhaps using complex submission publishing tools to build your reports? Investigational medicinal product dossiers (IMPD), clinical study reports (CSR), annual reports, training manuals, standard operating procedures (SOP) and even full 510k & PMA submissions could all benefit from a tool
How to save time and reduce risk by fully automating the creation of your reports Read More »
Thu, Jul 14, 2022, 3:00 PM – 3:30 PM CET Do you need to convert thousands of incoming emails and attachments to a standardized format such as PDF(/A) ? Manually tracking and processing emails, saving the message and attachments to PDF is a very time-consuming and expensive process. Today, this does not have to be
How to automate the conversion of incoming emails? Practical examples. Read More »
15 years of experience in automating, simplifying and speeding up document conversion. For all regulated industries. Rated 5 stars on Gartner’s Capterra platform.
