Our client, a Quality Assurance (QA) organization, had recently initiated a program to improve batch record format and layout. The ultimate aim of this initiative was to increase Right First Time (RFT), review lead-time performance and productivity by creating a simpler and more user friendly batch record.
Our Client, a large contract development and manufacturing organisation (CDMO) engaged us to support an extensive end to end order fulfilment project with the objective of significantly improving OTIF delivery performance.
The focus of this project was to address long and inconsistent lead-times for the release of product. The lab faced a particular challenge in the volatility of both mix and volume of workload.
This project was targeted to improve delivery performance (OTIF) to customer base, optimize capacity & productivity in the packing operation, provide improved visibility of upcoming workload for support functions such as QC & QA, and to re-engineer the planning process.
Our client, a leading pharmaceutical company, engaged us to help reduce their substantial overtime spending.
This project was targeted to improve the speed, quality and productivity of the QC functions at individual sites to contribute to a more stable supply of product. Additionally, it focussed on development of a standard capacity planning tool and process to provide visibility of resources at the site and network level.
The objective of this program was to improve laboratory efficiency and effectiveness through the utilization of lean tools and principles. It covered a range of GMP laboratory types including analytical chemistry, microbiology, environmental monitoring, incoming materials and in process control.
Reduce the overall lead time from manufacture of the product to final release (Quality Control and Quality Assurance).
Our client, a leader in the third-party contract testing field engaged us to improve the throughput time from sample receipt to COA approval. This environment is quite a challenging one given the paucity of forecast data and the need for a dynamic, flexible workforce to meet challenging customer turnaround times. Additional foci of the project included the creation of standardized roles and a robust and consistent capacity planning process.
The primary objective of this project was to reduce batch record review and disposition times to facilitate accelerated release of product to market. Ancillary objectives included increasing QA team productivity through implementation of capacity planning and standard work and streamlining of deviation management processes.
Our client, a leading pharmaceutical company, engaged us to increase project workload capacity at their Research & Development (R&D) facility whilst improving the schedule adherence of current project workloads. The project was charged with optimizing and increasing the utilization of advanced bioreactor laboratories, at a site that was responsible for the development of the next generation analogues of a portfolio of biological derived (large molecule) drugs, including one $6 billion/year blockbuster.
This project was targeted to improve the speed, quality and productivity of the QC function at a site manufacturing nutrition premixes. Additionally, it focused on development and installation of a standard performance management process.
The purpose of the program was to improve overall laboratory performance in the areas of quality, productivity and analyst engagement. Targets were specific to individual sites, dependent on complexity and level of lean maturity. A further aim of the program was to improve communication with and visibility to global functions of operational performance.
The focus of this project was to improve throughput times from sample receipt through testing and review. An additional objective was to increase right the first time for test execution and decrease time samples spend in review.