Most Life Sciences organizations appreciate by now that the push to data-driven Regulatory processes, and Regulatory Information Management (RIM), has a purpose far beyond that of satisfying the way the authorities want to work. This is about transforming the...
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RIM
Holistic RIM: Maximizing the value of regulated data
WEBINAR ON DEMANDHolistic RIM: Maximizing the value of regulated dataThis webinar will provide: The arguments for data centricity in regulatory information management, including data-first processes and workflows, are already well accepted. But what many companies...
Amplexor Life Sciences to exhibit at forthcoming Indian Pharma Regulatory Summit 2023
We will be exhibiting at this year’s Pharma Regulatory Summit 2023. Amplexor executives will be on hand to discuss some of the Indian industry’s latest developments. The sixth Annual Pharma Regulatory Summit 2023 brings together leading global pharmaceutical industry...
Amplexor Life Sciences to exhibit at forthcoming DIA Europe 2023
We will be exhibiting at this year’s DIA Europe 2023. Senior Amplexor executives will be available to discuss some of the industry’s most important trends. For 35 years, DIA Europe has been the largest neutral event in the European life science industry – the...
Visit us at DIA North Bethesda
We will be exhibiting at the this year’s DIA Regulatory Submissions, Information, and Document Management (RSIDM) Forum. Senior Amplexor executives will be available to explore some of the industry’s most pressing questions. The Forum features four tracks: Regulatory...
5 Major Efficiency Boosts for Your Regulatory Operations
A modern, holistic, end-to-end regulatory information management (RIM) system can help to greatly improve the efficiency of regulatory data, content and process management, deliver substantial cost savings, and enhance the quality of final output. Without a modern...
Visit us at the 2nd Pharmaceutical Regulatory Affairs Summit
We will exhibit at the forthcoming 2nd Pharmaceutical Regulatory Affairs Summit, which will be held in Vienna on 26-27 October. The Summit is designed to explore the most interesting regulatory topics of 2022, including regulatory status during COVID-19, decentralised...
Visit us at TOPRA 2022
We will exhibit at the forthcoming TOPRA Annual Symposium in Vienna on 17-19 October. The Symposium, which encompasses human pharmaceuticals, medical devices/IVDs and veterinary medicines, brings together key regulatory professionals from big pharma, small and...
5 Major Efficiency Boosts for Your Regulatory Operations
This webinar will focus on 5 capabilities that a modern holistic RIM system can provide to greatly improve efficiency of regulatory data, content and process management and consequently incur substantial cost savings while retaining same or even increase the quality of final outputs.
Visit us at RAPS Convergence 2022
RAPS Convergence 2022 returns in-person, bringing industry professionals and regulators together to co-create, problem-solve and discuss global and local challenges facing professionals in the regulatory life sciences community. It will be thrilling to return to a...
Visit us at DIA 2022 Global Annual Meeting
For the first time in several years, the DIA 2022 Global Annual Meeting returns in-person, bringing industry professionals, regulators, academics and patients together to co-create, problem-solve and discuss global and local challenges facing professionals in the life...
IDMP SPOR: Argh! So much is changing – now what?
EMA’s latest shift in its IDMP implementation guidance has been well documented. At the coal face, it’s causing all kinds of confusion as pharma companies try to figure out what they should do now. At Amplexor BE THE EXPERT 2022, K2 Consulting’s Kelly Hnat will draw on her ‘insider’ knowledge as an active participant in the EMA SPOR Task Force and member of the EMA PMS Process Focus Group, to provide some welcome clarity.