This article is the second in a series that will reflect on the activities that can or should be initiated now or soon in order to be prepared for the first IDMP reporting deadline in 2017. This second article reflects on high level IDMP Program planning. Even though the scope for the first IDMP reporting …
This article is the first in a series that will reflect on the activities that can or should be initiated now or soon in order to be prepared for the first IDMP reporting deadline . This first article reflects on IDMP IT System architectures options. Even though the scope for the first IDMP reporting is …
Read moreReflections on possible IDMP IT System Architecture options
With EMA’s publication (slide 25) of their current plan to facilitate the implementation of the International Organization for Standardization (ISO) identification of medicinal products (IDMP) standards as with Article 57(2) of Regulation (EU) 726/2004 and considering that EMA has communicated that the first iteration implementation of the Product Management System (PMS) will mainly include xEVMPD data – the …
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In PharmaIT we want to deliver Competitive, Experienced and Professional IT Consultants to the Pharma Industry. We aim to cover IT Management, Program and Project Management, Business Consulting, Test, Validation and Technical Consulting. We have a low cost base and therefore we can offer competitive rates. Should you be interested in getting more information please contact …
In PharmaIT we are looking to engange with Expirienced Consultants that wants to focus on delivering services to customers. We do not spend time on developing sales offerings or business service development, we focus on using our many years of expirience to produce deliverables and help our customers via consulting, projects or supporting running IT …