APT, ARCS, ARID, ARIM, Conferences

Speaker’s Corner, 4Q 2018

Joel Finkle will be speaking at the Drug Information Association (DIA) eDM 2018 – Clinical and Regulatory Operational Excellence Forum in Barcelona Spain, November 29-30, 2018. He will be speaking on the intersection of Component-Based Authoring (CBA) and Regulatory Information Management (RIM), in a presentation titled, “All the Way Around the RIM: From Registration Data to Documents to Dossiers and Back.”  If you’ve been hesitating on implementing documents containing structured data because the standards aren’t there, give a listen: it’s not about structured data submission, it’s about improving quality and productivity.

Also, please join ACUTA (an IQVIA company) at the  RAPS Convergence Conference in Vancouver, British Columbia, October 1-4. We will be exhibiting in booth 638. Come and talk to us about your plans for implementing Regulatory Information Management, ways of improving your throughput of submissions with ARCS outsourced publishing services, and tools for improving your document preparation processes with ARID and APT.

Contact us for more information on these products and services, or if you would like to meet with us at the upcoming conferences.

Soapbox image credit: “Daretoeatapeach

Author: Joel Finkle

Joel became embroiled in electronic submissions when regulatory came downstairs and asked "Can we convert all our clinical study reports to WordPerfect format for the FDA reviewer?" and he didn't say, "No." Since then, he's been involved with custom CANDAs, PDF publishing, eCTD, document template automation, Regulatory Information Management, HL7's RPS, and the ISO IDMP standard. He joined ACUTA in April of 2017. He'd share some of his famous tomatillo salsa with you, but he can't carry it on airplanes.

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