Get Your Records Retention Schedule Under Control — And Keep It That Way: A Case Study in Global Retention Scheduling

Developing an international retention schedule is a major challenge, but for Zasio it’s what we do every day. During this co-sponsored webinar with ARMA International, our presenters will walk you through a case study on global retention scheduling involving a major pharmaceutical contract organization, PRA Health Sciences.  You’ll see the step-by-step process used, and see…

Webinar: A Case Study in Global Retention Scheduling

Developing an international retention schedule is a major challenge, but for Zasio it’s what we do every day. Join ARMA International, the world’s leading community of informational professionals, and Zasio, a leading provider of Records Management and Information Governance solutions, for a case study on one of those projects involving a major pharmaceutical contract organization,…

New Changes to the European Union’s Medical Device and In Vitro Diagnostic Device Regulations

On May 26, 2020, the European Union enacted new regulations concerning medical and in vitro diagnostic devices—a move that should cause manufacturers, clinical trial sponsors, investigators, and other regulated parties involved in medical device development, manufacture, and distribution in the EU to take notice. These new regulations replace existing directives and bring about many changes,…

bronze key resting on a keyboard with a finger about ready to press a large red key with the words personal data

GDPR Compliance Prep for US Companies

The clock is ticking on the European Union’s new privacy law, the General Data Protection Regulation (GDPR). We’re less than one year away from when the GDPR comes into force, May 25, 2018. This new regulation imposes sweeping privacy protection requirements on any entities that oversee personal data operations or process personal data in the…