Upcoming Events

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eRegulatory Summit.

Joel Finkle of ACUTA will be presenting at this event! This meeting in Lisbon, Portugal is focused on IDMP – Identification of Medicinal Products, a standard for drug registration data being implemented initially in Europe. ACUTA’s Joel Finkle will be speaking on how to prepare for implementation of this standard by building a Regulatory Information Management database of registrations

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RAPS Regulatory Convergence 2018.

The Regulatory Affairs Professional Society’s annual meeting is in Vancouver in 2018, and will have key discussions on regulations and processes for managing medical products including drugs and devices. Join us in the exhibit hall to discuss how you can improve processes and reduce costs by implementing ACUTA services and systems.

Past Events

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DIA RSDIM 2018

This is the primary DIA symposium for regulatory operations, publishing, and regulatory information management. Join ACUTA in the exhibit hall to discuss how the processes and technologies discussed at the meeting can be implemented for your enterprise

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Webinar.

Joel Finkle of ACUTA LLC will be conducting a webinar with a focus on Compliance Key: IDMP Data Collection.

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Joel Finkle and Donald Palmer will represent ACUTA at the Annual DIA Canadian Conference.

The DIA Annual Canadian Meeting will reflect on the evolution of Canada's health system by bringing together key thought leaders from industry, academia, regulators, and Health Canada.

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Carl Hackett will represent ACUTA at the EMA eCTD 4.0 Working Group.

The eCTD v4.0 working group would like to offer an opportunity for all eCTD tool vendors to discuss open points and ask questions on eCTD v4.0 EU Module 1 Implementation Guide. A face-to-face vendor meeting is planned to take place at BfArM in Bonn, Germany on 6th of October 2017. All vendors are invited, at their own cost to take part. All participants must register in advance, by 22nd September 2017, via email to eCTD4consultation@ema.europa.eu.

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Join the brightest minds in regulatory at the annual RAPS Regulatory Convergence.

See the global regulatory community in action. Intensive workshops. Topical sessions. Meet ups with regulators. This is where it all comes together.
Visit us at the Exhibit Hall.

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eRegulatory Summit - RIM, IDMP and Global eCTD.

Connecting RIM, IDMP and eCTD professionals to drive regulatory strategies through authority access and industry expertise.
Visit us at our booth #15.

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TOPRA India 2017: Building Regulatory Excellence

TOPRA India is a two day congress in Bangalore that will focus on how pharmaceutical organisations in India can build regulatory excellence on the global stage.
Visit us at the Exhibit Hall.

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6th Annual Regulatory Operations and Submissions Conference

Optimizing the Development of Quality Product Submission Dossiers with a Comprehensive Understanding of Regional and Global Dossier Requirements, Ensuring Dossier Navigability and Current Publishing Technologies
Visit us at the Exhibit Hall.

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Regulatory Submissions, Information, and Document Management Forum 2017.

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2nd Annual IDMP Update Forum

DIA

Explore the Complexities of RIM and IDMP Data Gathering

DIA

Regulatory Submissions, Information, and Document Management Forum.

RAPS

2015 RAPS Convergence

DIA

eRegulatory and Intelligence Annual Conference.