Meet Turn Around Time of Samples, Analyst Productivity and Chemicals Forecasting
Meet Turn Around Time of Samples, Analyst Productivity and Chemicals Forecasting
Life Sciences companies include Pharmaceutical, Contract Development and Manufacturing Organization (CDMO), Biotechnology, Contract Research Organization (CRO) and Biosimilars continue to operate in a highly competitive environment. The Quality Control (QC) laboratory in a pharmaceutical company plays a critical role in the testing of Raw Materials, Stability, In-process and FG Samples. QC Analysts from different sections analyze incoming samples of different kinds. These include Finished Goods (FG), in-process products, stability samples, and environmental samples. Analysts may also be required to analyze raw materials.
In organizations with diversified drug products, the number of samples to be tested per week will range from 150 – 400 Samples and each sample must go through a minimum of 6 tests. In such a scenario it is a challenge to prioritize the samples and assign equipment like HPLC/GC to the QC Analyst manually.
HOD’s of QC Labs are under steady pressure to improve the lab operations in order to meet the Sample TAT (Turn Around Time). The equipment used in the Pharmaceutical and Biotech product testing are highly sophisticated, extremely sensitive, and very expensive. Maximizing both staff (Laboratory technicians and managers) time and machine time is essential in the QC lab to address the problems of varying demands and to maximize resource efficiency.
Consequently, Planners/Managers are finding a way to move towards lean QC lab by improving their processes, improving effective utilization of resources, reducing lead times, and at the same time, increasing reliability by accelerating authorization processes for compliance. This affects both production and batch release.
A good Quality Control Planning describes how an organization will achieve its quality goals by specifying the quality assurance and control activities which are performed as part of daily lab operations
In order to avoid the complexity of scheduling, an ideal solution is required to minimize the time invested by the workforce in carrying out their tasks. It is also important to increase flexibility in processes allowing changes in schedules based on demand and optimizing the lab efficiency, performance in terms of test cycle times and on-time deliveries.
AmpleLogic QC Planning and Scheduling Software is a web-based solution designed on LOW CODE NO CODE APP (LCNC DEVELOPMENT ) PLATFORM specifically for Quality Control and R&D Laboratories. It helps you to plan and schedule your resources, track the laboratory activities and generate user configurable reports for swift decision making. Features like resource scheduling, sample batching/ campaigning helps in moving towards lean QC lab practices.
AmpleLogic QC Planning and Scheduling Software is a solution for organizations that aim to improve lab efficiency by introducing automatic calculation of efficiency of every analyst by studying the completed samples or actual tests performed by them. This feature enables both analysts and management to track their individual performance and efficiency. It also provides with an overview of the reasons for delay, and for time consumption by the analyst. This QC Lab Planning Automation Software provides insight to identify whether the analyst requires additional training and list of challenging tests in the labs.
With the help of the Resource Planning and Scheduling Software a lab technician or an instrument can be blocked to analyze or investigate. This reduces the number of deviations or non-conformance for the organization.
AmpleLogic QC Lab Scheduling Solution will allow you to connect from anywhere any time. Ensures data integrity, regulatory compliance, and traceability. AmpleLogic QC Planning and Scheduling Software complies with FDA 21 CFR Part 11, MHRA, EU Annex 11 and other applicable regulatory standards.
QC Lab operations can be efficiently planned by automatically grouping all samples, creating short term and long term schedules constrained by lab resources.
| PERFORMANCE REPORTS | |
|---|---|
| Analyst task report | Instrument Occupancy |
| Occupancy of Analyst | Sample wise |
| Grouping wise | Schedule Test wise |
| Resource Utilization | Instrument Utilization |
| Column Occupancy | No. of usages on columns |
AmpleLogic QC Planning and Scheduling Software will support the head of departments, managers, and supervisors in allocating the different tests required to release different samples to various analysts, based on critical, due date, work-load and other parameters
GMP Compliant QC Planning Software also complies with electronic Record standards defined by TGA, CDSCO, HEALTH CANADA, MCC, ANVISA, EMEA, SFDA, NAFDAC, MEDSAFE, MHLW, MCAZ, SWISSMEDIC, KFDA, and MoH.
To learn more about how AmpleLogic QC Planning and Scheduling Software can help Life sciences and Pharmaceutical QC Labs and R&D Labs to increase their on-time delivery and lab efficiency, please contact us