AmpleLogic’s QC Planning and Scheduling Software enhances efficiency in QC labs across Life Sciences industries, including Pharma, Biotech, CROs, CDMOs, and Biosimilars. With up to 400 samples tested weekly, our software streamlines resource allocation, prioritizes tasks, and maximizes equipment usage like HPLC/GC, ensuring timely sample analysis and regulatory compliance. It minimizes manual intervention, reduces lead times, and improves operational efficiency by automating workflows. Designed to meet FDA standards, AmpleLogic helps QC teams achieve higher reliability, accelerate batch release, and optimize lab resources, ultimately driving both speed and quality in pharmaceutical manufacturing.
Efficiently plan, schedule, and track lab activities with minimal effort
Maximize the productivity of analysts and the utilization of instruments for seamless operations
Gain instant insights into lab performance, resource allocation, and utilization
Ensures adherence to regulatory standards such as FDA 21 CFR Part 11, MHRA, and EU Annex 11
AmpleLogic QC Planning and Scheduling Software is a web-based solution designed specifically for Quality Control and R&D Laboratories. It helps plan and schedule resources, track lab activities, and generate customizable reports for quick decision-making. With features like automated resource scheduling, sample batching, and real-time performance tracking, it enhances lab efficiency and supports lean QC practices. The real time scheduling software allows organizations to:
Automatically assign tests based on analyst availability, qualifications, and expertise
Generate customizable reports to drive informed, data-driven decisions
Ensure compliance with comprehensive audit trails and electronic signatures
Access the system from anywhere, at any time, for continuous operations
Manual QC planning and scheduling in pharmaceutical labs often leads to inefficiencies and errors, especially when dealing with high volumes of samples and complex schedules. Common pain points include the cumbersome task of manual data entry, difficulty managing resource allocation for varying sample types (finished goods, raw materials, stability, etc.), and the challenge of rescheduling tasks, particularly for retests or out-of-spec (OOS) scenarios. These issues often lead to operational delays, high labor costs, and increased risk of human error. Without real-time visibility, managing instrument calibration, workload distribution, and the availability of qualified analysts can be time-consuming and error-prone, directly impacting test cycle times and on-time deliveries.
AmpleLogic QC Planning and Scheduling Software offers a solution by automating and streamlining these processes. The software provides real-time scheduling, resource allocation, and performance tracking, allowing QC managers to optimize workloads, manage analyst performance, and ensure equipment availability with ease. With features like automated test scheduling, report generation, and compliance with global standards (FDA, MHRA, EU Annex 11), AmpleLogic minimizes manual input and operational costs, improves accuracy, and enhances overall lab efficiency. It also offers flexible scheduling capabilities to handle shifting priorities and urgent tasks, improving turnaround time (TAT) and boosting productivity.
AmpleLogic Lab Equipment Scheduling Software offers a comprehensive set of features to transform QC lab operations
Create shift-based plans with resource availability consideration. Effortlessly schedule and reschedule daily lab activities.
Plan tests with accurate resource needs for optimal lab efficiency. Create schedules with a single click based on unique organizational requirements.
Group samples based on pre-defined criteria for efficient analysis. Prioritize urgent analyses with separate test schedules.
View daily, weekly, monthly, or annual schedules for analysts. Color-coded schedules for easy identification of critical tasks and delays.
Get instant insights into lab performance and resource utilization. Customizable reports for tracking individual and overall lab efficiency.
Automated communication for scheduled activities and escalations. Keep analysts informed and aligned with scheduled tasks.
Automatically block resources during OOS or Root Cause analysis. Ensure transparent and complete view of lab performance.
View tasks assigned to analysts, time spent, and estimated durations. Optimize resource allocation with real-time data.
Complete Auidt Trail, electronic signatures, and field-level security. Complies with FDA 21 CFR Part 11, MHRA, EU Annex 11, and other standards.
Create reports, charts, and dashboards tailored to specific needs. Monitor key performance indicators based on samples, completion times, and employee performance.
Compliance with Turnaround time (TAT), a key performance indicator for laboratory performance
Create Out of Specification reports following user-defined templates
Task scheduler guided by analyst insights orchestrates efficient workflows with precision
Scheduled equipment blocking ensures efficient resource allocation and minimizes operational disruptions
Track machinery utilization, get insights into equipment downtime and usage patterns for streamlined production planning
Biometric attendance system enhances efficiency and accuracy in tracking attendance data
Provides real-time data for resource allocation to address issues with shortfalls or excess resource allocation promptly
View equipment usage and availability for allocation in real-time in the weekly schedule
Auto-generated weekly/monthly reports and KPI-based infographic dashboards for monitoring key performance indicators
Automatically generates daily, weekly, or monthly schedules for resource tracking
Groups different samples together based on product grouping and campaigning, reducing overall test time
Track QC analyst or instrument availability in real-time for optimal resource allocation
Automatically schedules tests by checking analyst’s availability, qualifications, and experience level
Industry-Specific Software for Enhanced Quality and Compliance
Pharmaceutical quality control (QC) is the backbone of ensuring product safety, efficacy, and compliance. However, managing QC laboratory processes in the pharmaceutical industry presents a
QC heads often face trouble while planning and tracking Quality Control tests in their labs. They have to plan numerous tests every day to ensure
Quality control planning and scheduling is an important function for keeping laboratory processes on track in the pharmaceutical, biotech and the Lifesciences industry. The task
Yes, it adheres to FDA 21 CFR Part 11, MHRA, EU Annex 11, and other global regulatory standards.
The software tracks individual analyst efficiency, identifies delays, and provides insights for improvement.
Yes, AmpleLogic QC Planning Software easily integrates with ERP, legacy systems, and other data sources.
The software allows separate test schedules for urgent analyses based on predefined criteria.
AmpleLogic QC Planning Software provides a clear, prioritized schedule, supports allocation based on criticality, due dates, and workloads.
AmpleLogic QC Planning Software provides a clear, prioritized schedule, supports allocation based on criticality, due dates, and workloads.
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