Electronic Signature Legitimacy for Life Sciences in European Union

How to eSign a document: electronic signature legitimacy for Life Sciences in European Union

the expense and time required for clinical trials continue to rise resulting in shorter patent exclusivity periods and lost revenue sponsors and CRO s are looking for technology to increase efficiency digital signatures improve clinical operations in three important ways first by enabling site personnel and I arbys to access sign and submit documents required for site initiation II clinical portals equipped with digital signature functionality allow sponsors and CRO s to complete site initiation in weeks instead of months second site monitoring reports most have to be submitted within a certain number of days after a visit and it's not unusual to run up Express Mail charges in the many thousands by enabling these reports to be sent electronically digital signatures cut routing costs and delays instead of wasting time processing paperwork monitors can concentrate on the quality of their reporting third audits cost more and take longer when you have to track down paper records than they do when you've got a secure repository of digitally signed electronic records digital signatures are accepted by regulators and courts worldwide as proof of identity and intent of the signer and that the documents content has not changed the technology can enhance any mainstream document management system leveraging its ability to speed up track and audit the flow of documents and clinical operations learn more about how to speed up site initiation and reduce site monitoring and audit costs and the many other ways implementing digital signatures can improve clinical operations efficiency you