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Automated Proofreader

Error detection and verification for printed materials in regulated life sciences, comparing documents against master files to ensure accuracy and compliance.

Overview

Novatek International's Automated Proofreader (Nova-APR) is a proof reading software solution designed for healthcare and life science organizations that depend on accurate product information documents and printed labels to communicate with end users. By automating the comparison and verification of printed materials against pre-approved master documents, Nova-APR eliminates the errors, fatigue, and inefficiencies associated with manual proofreading processes, holding customer communications to the same standard of safety and accuracy as the products themselves.

Nova-APR operates through a comparison method, scanning all incoming printed materials against a master document to detect any discrepancies across text, graphics, and color. The software is capable of proofreading virtually any file type — from multilingual text documents and images to graphics and even Braille content — making it a versatile solution for pharmaceutical, biotechnology, and broader life science organizations seeking to simplify and accelerate their proofreading workflows. The solution is fully 21 CFR Part 11 compliant and includes an extensive, independent audit trail.

Features and Functions

  • Automatic batch verification of incoming materials against a pre-approved master document
  • Capable of detecting the smallest of errors, including missing or incorrect text, font type and size, color discrepancies, and location changes
  • Includes an extensive and independent audit trail to support regulatory compliance
  • Capable of operating with minimal supervision, seven days per week
  • Able to analyze a predefined number of samples per run
  • Supports Braille content inspection in addition to standard text and graphic formats

Key Benefits

  • Language independent, enabling inspection of multilingual printed materials without restriction
  • Eliminates manual verification methods, reducing the time and cognitive burden placed on staff
  • Increases efficiency and productivity by proofreading numerous pages in a fraction of the time required by manual processes
  • Reduces human error and guarantees a higher level of accuracy in product information delivery
  • Streamlines and accelerates the approval process for labels, cartons, inserts, leaflets, procedures, and contracts

Supported Document Types and Use Cases

  • Product labels and cartons
  • Package inserts and leaflets
  • Standard operating procedures and contracts
  • Multilingual text documents and graphic files
  • Braille printed materials

Nova-APR is a process-driven, 21 CFR Part 11 compliant solution purpose-built for regulated industries. Its language-independent architecture and advanced inspection technology make it particularly well suited for pharmaceutical and life science organizations looking to improve the accuracy of distributed product information while meeting the highest regulatory and quality standards.

Meta

Domain
Quality, Compliance & Regulatory
Subdomain
Quality Management System (QMS)
Software type(s)
Workflow Automation
Deployment type(s)
On-Premise
Industry vertical(s)
PharmaBiotech
Development stage(s)
ManufacturingPost-Market & RWE
Target user(s)
Lab Manager / Core Facility ManagerQA / Regulatory Affairs
Compliance standard(s)
21 CFR Part 11GxP