Is my new production method approved? What is the first batch implementing my product-update? Most companies still align their regulatory and production operations through phone calls and good old hard work. But bigger operations, increasingly complex supply chains and the ever changing regulatory landscape of 21st century pharma demand 21st century solutions. Connecting your RIMS […]
Read moreWebinar Materials – Integrated information management
Published onIn this webinar, we have illustrated the role of Identification of Medicinal Products (IDMP), Regulatory Information Management System (RIMs), Structured Content Authoring (SCA) and Enterprise Resource Planning (ERP)-RIMs integrated approach towards global interoperability. Below you will find all the webinar materials, this include the webinar recording, as well as the webinar slides. In addition, we […]
Read moreDIA EuroMeeting
Published on
Come meet us at DIA EuroMeeting 2017! From 29 – 31 March, we will be exhibiting at the DIA EuroMeeting 2017 in Glasgow, United Kingdom.
Read moreBeing the future
Published on
Intro: Innovation is the word that best describes the Dutch Pivot Park Community. Pivot Park is a young and energetic research centre in the field of Life Sciences, with a focus on new drug development. In an interview with Mirjam Mol, director of Pivot Park Oss, we discuss the trends and developments in the life […]
Read moreIperion NEN7510 certified
Published onIperion is proud to announce that it recently passed the directives of the NEN 7510 Certificate. The NEN7510 is a standard developed by the Dutch Standards Institute for information security for the healthcare sector in Netherlands.
Read more