Products – Quickflow

All the software you need to run your business

Explore our 15+ Applications, compliant with USFDA

Quickflow - LIMS

Effortlessly orchestrates laboratory workflows, guaranteeing adherence to compliance standards and adeptly overseeing the complete test request lifecycle, seamlessly navigating from test request initiation to COA issuance.

Quickflow e-Sheet

Adeptly automates laboratory calculations, converting them into intuitive web-based forms with meticulous access control and finely gained permissions, ensuring a secure, efficient environment for precise and compliant data handling.

Genius Lab

Optimize scientific workflows with seamless integration of standalone instruments, utilizing RS232 or ethernet connectivity for enhanced data flow, ensuring efficient synergy, and precision in your processes.

eSPM

Say goodbye to manual QC planning and embrace our cutting-edge automation solution for faster turnaround times and maximized lab efficiency.

Quickflow Column Management System

Optimizes chromatography columns from procurement to performance monitoring, ensuring lab efficiency, compliance, and enhancing pharmaceutical manufacturing quality.

Quickflow Standard Management

Meticulously oversees laboratory standards, ensuring regulatory compliance and enhancing accuracy, traceability, and reliability in pharmaceutical testing and analysis.

Quickflow Logbook

Digitizes traditional logbooks in Pharma, Bio tech, and Life Science, allowing secure electronic recording of activities like equipment usage, calibrations etc.,

Quickflow Chemical Management System

Systematically oversees and controls the entire lifecycle of chemicals in laboratory or manufacturing from indent to disposal, ensuring compliance with safety regulations and industry standards.

Quickflow Loose Sheet Management System

Efficiently organizes and manages unbound documents in a digital format, facilitating the tracking, storage, retrieval, and organization of loose sheets with enhanced security and accessibility.

Quickflow APQR

Automates and streamlines the Annual Product Quality Review process, enabling systematic and comprehensive assessment of product quality data for informed decision-making

Quickflow Alarm Trending Management

Monitors, analyzes, and manages Critical and Non-Critical alarms, enabling proactive issue identification and continuous improvement of operational reliability by tracking trends and patterns over time.

Quickflow CPV

Monitoring application enables real-time data collection, analysis, trending and reporting to ensure pharmaceutical processes consistently meet predefined quality criteria.

Quickflow BMR

Innovative software with customized templates for digital oversight of Batch Manufacturing Records, revolutionizing workflows by seamlessly integrating, streamlining processes, and eliminating paper-driven procedures.

UAM

Employs a holistic approach, utilizing Robotics Process Automation to streamline the issuance, modification, revocation, and review of user access rights, fortifying security measures, optimizing IT efforts and enhances productivity.

QCMS-FMS

 A strategic solution insure data integrity of scientific core raw data of non-chromatographic, standalone instrument used for QC analysis.

Quickflow ELN

The digital evolution of lab notebooks streamlines data recording, enhances collaboration, and ensures meticulous compliance with rigorous laboratory standards for advanced research documentation.

Quickflow WMS

Optimizing the entirety of the inventory management lifecycle, it orchestrates processes spanning from indenting to disposal for a diverse array of materials, guaranteeing operational efficiency, precision, and stringent compliance.

Quickflow DMS

With audit trails and version control, our system optimizes pharmaceutical document processes, including SOPs, STPs, Protocols, and more. This enhances control, organization, and accessibility, revolutionizing documentation practices.

Quickflow QMS

Efficiently manages and streamlines pharmaceutical quality processes, including change controls, deviations, CAPA, market complaints, and OOS, enhancing precision and efficiency while ensuring compliance and real-time visibility.