ACUTA

ACUTA joins IQVIA

IQVIA + ACUTA

We are excited to announce a new chapter for our customers and our company. As of July 13, ACUTA has become part of IQVIA, a leading global provider of information, innovative technology solutions and contract research services focused on using data an science to help healthcare clients find better solutions for the patients.

This marks an important step in ACUTA’s mission to be the partner of choice for life sciences and related industries, by helping you collect, manage, and share regulatory information through innovative, cost-effective, reliable, and globally-accessible solutions and services. We look forward to the opportunities the combined organization will provide our customers. We expect the added resources of IQVIA will enable us to provide better around-the-clock support, and help accelerate our technology pipeline to deliver more capabilities to you in our flagship ACUTA Regulatory Information Management (ARIM), as well as the technology implementation and integration services including master data management.

IQVIA and ACUTA fit together well: while we both serve the regulatory space, we provide very complementary solutions. ACUTA brings (in red, below), technologies and services that complement IQVIAs (in purple) to support clinical and regulatory requirements from molecule to market (this is far, far from a complete list of solutions).

We are looking forward to joining IQVIA – the entire ACUTA leadership team is continuing with the new organization and we are excited about the opportunities this brings to our employees and customers in the coming months.  Your business is very important to us. ACUTA will continue with its existing offerings, and we will work to ensure that you do not experience any disruptions in our services, or our relationship with you. ACUTA’s business development team will be contacting each of our customers directly, but please do contact us  if you have any questions about how we can assist you with your regulatory requirements with ACUTA as an IQVIA company.

 

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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