Simplifying the Process Instruction program rollout We are excited to announce that the latest version Opcenter™ Execution Pharma v. 2205…
Delivering an enhanced RESTful API for improved productivity, efficiency and quality We are excited to announce that the latest version…
Supporting greater collaboration and improving operational efficiency We are excited to announce that the latest version of Opcenter Execution Medical…
Providing a paperless solution for the life sciences/pharma industries! We are excited to announce that the latest version Opcenter™ Execution…
The New Regulation (EU) 2017/745 for medical devices (MDRs), which went into effect on May 26, 2021, is a major update to the regulatory framework in the European Union (EU).
Today’s disruptive market scenarios, the unknown consequences of COVID-19, increasingly sophisticated personalized, and the new FDA and EU Regulatory implications…
The COVID-19 pandemic has disrupted global supply chains on a monumental scale, rushing all MD&D manufacturers to quickly re-adapt and respond to new challenging market scenarios.
Delivering a new RESTful API, an advanced framework and improved configurability We are excited to announce that the latest version…
Terumo Americas is a global leader in medical device industry manufacturing life-supporting and sustaining Class III devices across four divisions over the last 50 years, including interventional systems, injection and infusion therapy devices and drug delivery devices.
