Chemical & Process Manufacturing

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Continued Process Verification

qSync™ is an AI and machine learning software that digitizes end-to-end batch records for Continued Process Verification (CPV) without changing your existing qualified process...and without making expensive and risky system changes.

Mareana combines handwriting recognition, AI text analytics, a flexible, repeatable query engine, and a deep understanding of CPV and associated processes and technology to digitize your process and allow your team to focus on value-added analytics, not data wrangling.

 
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Identification of Medicinal Products (IDMP)

Completing hundreds of fields of information for up to thousands of products can challenge even the most experienced pharmaceutical manufacturing compliance lead. qSync by Mareana for IDMP compliance reduces compliance resources, saves countless labor hours, improves data accuracy, and accelerates the entire compliance process.

qSync by Mareana can jump start your IDMP project with 52 of the first 79 required fields already completed.

 

Regulatory Affairs

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Quality Operations

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Clinical Trials Management

Mareana developed a qSync™ analytical solution to help clinical study supply professional manage Investigational Product (IP) kit supply and logistics across multiple studies with numerous CRO’s even when IRT systems or other data sources (like excel, pdf) are not integrated.  Study supply professionals can now ensure that patients are provided the right dosage and strength at the right time.

 

Product Lifecycle Management

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Discard Reduction

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