Iperion Life Sciences Consultancy will be present at the DIA 2019 Global Annual Meeting in San Diego, held from June 24-26. Visit us at booth #819! After the success of last years visit, we are also present in 2019. The focus on our booth is about making a plan for digitalization and regulatory information management. […]
Read more4 steps towards ERP-RIMS interoperability
Published onIs my new production method approved? What is the first batch implementing my product-update? Most companies still align their regulatory and production operations through phone calls and good old hard work. But bigger operations, increasingly complex supply chains and the ever changing regulatory landscape of 21st century pharma demand 21st century solutions. Connecting your RIMS […]
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 moreWe C.A.R.E.
Published onIperion Life Sciences Information Systems understands the importance and value work talent. Providing them with opportunities to learn, grow and contribute to life sciences industry continues to be one of our priorities. Our organization started a special program, C.A.R.E. to optimize recruitment, to empower the employees and to work on binding in the long run. The program […]
Read moreArticle: An expanding universe
Published onCan we still stop the expanding universe of regulations in life sciences? That will be difficult but necessary. Otherwise regulation is only creating a bogus safety, states professional Tanja Hoffman. A conversation with an experienced professional about her vision on the regulation in the life sciences industry the upcoming decade.
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