Icon-Structured-AuthoringIn 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 you mitigate such business challenges.

In this web series we will address the following topics:

How to optimize the use of your RIM? (Completed)
Our experience with RIMS business implementation

    From experiences, we noticed an unmerited amount of focus on the technical and validation aspects of RIM implementation, rather than looking at how such technologies can be utilized best to facilitate business needs. Discover how Iperion has helped clients re-position their RIMs.

  • Date: Tuesday 17 October, 2017
  • Timeslots: 10:00-11:00 CEST or 17:00-18:00 CEST (Completed)
  • Webinar Materials: Click here.

IDMP now or later? (Completed)

    The pharmaceutical industry is very much aware of the delay of IDMP caused by Brexit. However, don’t let this take your attention away from the recently released data standards. Find out why IDMP is important for your business process development.

  • Date:Wednesday 15 November, 2017
  • Timeslots: 10:00-11:00 CET or 17:00-18:00 CET
  • Webinar Materials: Available Soon!

Improve your supply chain oversight (Register now!)
Advantages of linking your ERP and RIM data set

    End to end supply chain traceability is a commonly shared challenge for pharmaceutical manufacturers. Discover how ERP and RIM integration can facilitate supply chain efficiency.

  • Date: Thursday 07 December 2017
  • Timeslots: 10:00-11:00 CET or 17:00-18:00 CET
  • Register here!

Structured Content Authoring
Efficient document management

    Clinical and regulatory processes often involve numerous documents, such as SmPCs, PIs, IMPDs, IBs and many more. Typically these documents are in various versions and inconsistency is the key issue. Learn how Structured Authoring tools can facilitate the life cycle management of documents.

  • Date: To be announced

Integrated Information Management
Bring it all together!

  • Date: To be announced

Who should attend?

  • Life science professionals working or interested in the fields of regulatory compliance, structured authoring, IDMP and Regulatory Information Management Systems
  • Experts with an interest in data quality, data standards and business reporting
  • Decision makers that are interested in data driven decision making

Speaker

Frits Stulp

Frits Stulp

Managing Director Iperion Life Sciences Consultancy

Contact us for more information +31 73 648  8000 or send an email to webinars@iperion.nl