IDMP might not only be about compliance to EU commission regulation it is also a journey towards better and more data control across business areas in the pharmaceutical industry.
Read moreIperion and Pharma IT announce partnership in the delivery of full cycle IDMP services for the pharmaceutical industry
Published onIperion, a leading provider of consultancy services, information systems and IT services-GxP cloud computing for the life sciences industry, and Pharma IT, a provider of IT services and business consultancy announce a partnership to deliver quality IDMP consulting services for the pharmaceutical industry.
Read moreAttendance Global Pharmaceutical Affairs Summit 2015
Published onFrom 27-29 October the Global Pharmaceutical Affairs Summit will take place in Berlin, Germany. We will attend the IDMP & RIM focus day on October 29th.
Read moreDownload now and learn more: IDMP Compliance and IDMP phasing
Published onOur Managing Director Life Sciences Consultancy Frits Stulp hosted a webinar for a practical approach to IDMP compliance and views on dealing with the potentially new European IDMP phasing. We would like to share the presentation from this webinar with you now. Complete your form here and request a download now.
Read moreIperion present at Marcus Evans conference about IDMP Compliance Challenge and RIM
Published onDespite the fact that the regional implementation guidelines have not been published yet, decisions about the IDMP compliance preparations need to be already made today as this legislation will have major implications for all companies active in the industry and this means that there is a lot of work to be done within a very short timeframe.
Read moreFrits Stulp joins Iperion as Managing Director Consultancy
Published onIperion is pleased to announce that Mr. Frits Stulp has joined the company as of March 1st. In his role as Managing Director Consultancy Frits will be responsible for further development of the business unit Consultancy within Iperion.
Read more