The IDMP data standards aim to standardise the submission of data on medicinal products. Remco Munnik, Associate Director at Iperion, has been working with the EU focus group creating the EU IDMP Implementation Guide version 2, published late February. He explains why pharma companies need to act now in response to the new guidance and provides practical recommendations for action.
The EU Identification of Medicinal Products (IDMP) Implementation Guide version 2.0 (EU IG), for the submission of data on medicinal products, sets out the implementation requirements of the ISO IDMP standards in the EU and triggers the countdown to the implementation of IDMP in Europe. With the clock ticking, life sciences companies doing business in the EU need to start getting their data in order and processes in place. In addition to the data requirements of ISO IDMP, the new Target Operating Model (TOM) implies that existing processes within life sciences companies need to be amended to collect more
The Ultimate Study Guide for the DevNet IoT Certification
Do you know when the first thing was connected to the Internet of Things? Some could say it was 1982 and a Coke vending machine at the Carnegie Mellon University. Since then, the IoT has come a long way and is getting adapted more and more, especially with the ongoing IT/OT convergence.
But let s start simple: What does IoT exactly describe? Well, the main purpose of the IoT is to get digital presentations of analog things such as objects, environments, or systems. So basically, sensors are capturing analog events, turning them into digital data points which will then be collected in a data lake (sitting in the Cloud or data center).
Overview of recent webinar on the Africa Covid-19 vaccine financing and deployment strategy thepresidency.gov.za - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from thepresidency.gov.za Daily Mail and Mail on Sunday newspapers.
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While the COVID-19 pandemic made 2020 a trying year, one unintended benefit was that the Florida legislature allowed pharmacists to further expand their scope of practice to help patients with certain chronic conditions through collaborative practice agreements. Though, as discussed below, they did not make it easy.
The Board of Pharmacy (the “Board”) “collaborated” with the Board of Medicine and the Board of Osteopathic Medicine to develop rules addressing both collaborative practice and the test and treat protocols. The rules set forth in Chapter 64B16-31, Florida Administrative Code, became final on October 20, 2020. We previously addressed the scope of these arrangements a blog post,
7 January, 2021
Guidance on the Rights of Child Human Rights Defenders, written by Professor Laura Lundy from the Centre for Children’s Rights at Queen’s University Belfast, has recently been launched by Child Rights Connect.
The launch comes after a year-long consultative process in collaboration with Child Rights Connect, Queen’s University, the UN Committee on the Rights of the Child (CRC Committee), the Special Rapporteur on the Situation of Human rights defenders (SR on HRDs), many international child and human rights organisations and experts and child human rights defenders (CHRDs).
clarifies:
what is distinctive about CHRDs and the contexts in which they act,