Join Amplexor and Iperion in a webinar February 26th on RIM: Delivering Better Efficiencies Across Operations – Automating Multiple Systems and Streamlining Compliance Reporting.
Read moreIDMP as enabler for standardization, automation and interoperability
Published onImplementing IDMP can help your organization by gaining efficiency due to standardization, automation and interoperability. We define 5 stages in this process. 1.Consider structured product information as an asset for your organization 2.Make the transition from paper to high quality structured data 3.Enable the exchange between processes, functions and systems 4.Facilitate the exchange of […]
Read moreWebinar to prepare you for Medical Device Regulations (MDR) Part II
Published onThe new Medical Device Regulations (MDR), which come into force by May 2020, include new features, new requirements and far more details than the old medical device directives. To understand the risks imposed on your business continuation, it is time to know the implications and start preparations on time. Iperion and Amplexor will help you […]
Read moreWebinar to prepare you for Medical Device Regulations (MDR)
Published onThe new Medical Device Regulations (MDR), which come into force by May 2020, include new features, new requirements and far more details than the old medical device directives. To understand the risks imposed on your business continuation, it is time to know the implications and start preparations on time. Iperion and Amplexor will help you […]
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 moreWebinar Series – Practical solutions for information management
Published onIn the dynamic environment of the pharmaceutical industry, companies are imposed with inevitable challenges, dealing with complex systems, processes, technology, and on top that, regulatory requirements. In an effort to cultivate discussions on these underlying issues, Iperion has created a platform to share the lessons learnt, highlighting the best practices we have assimilated to help […]
Read moreIDMP Webinar: Pistoia Alliance, January 19th
Published onIperion is looking forward to share practical considerations in bringing IDMP data under control and usable for both submission and business purposes at the PISTOIA webinar coming Thursday, together with Edsel David, Andrew Marr and Martin Romacher! Hope you will join! Title: IDMP: It’s all about the patient: enhancing patient safety through improved R&D information […]
Read moreIDMP Webinar: Global strategies for implementation & Harmonization
Published on
Why IDMP? The business case for IDMP adoption varies company to company, region to region. They range from compliance to EMA mandatory timelines, preparation for the forthcoming FDA adoption, and recognizing the benefits for product development and expansion, to an opportunity to bring innovation to across domains.
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