Project Basecamp: Lab Instrument Qualification

Cell & Gene Therapy

Overview

With more than 140,000 square feet of space, ElevateBio BaseCamp includes current Good Manufacturing Practice (cGMP) manufacturing suites, analytics, and quality control (QC) laboratories, and protein engineering, virology, and immunology labs, all with state-of-the-art laboratory automation. BaseCamp was designed to support diverse gene and cell regenerative therapy products, with manufacturing suites that have flexible floor plans for cGMP manufacturing. The facility has autologous, allogeneic, and regenerative medicine cell products such as induced pluripotent stem cells, or iPSC, and viral vector manufacturing capabilities. Additionally, the BaseCamp cGMP manufacturing suite environment, equipment, and processes are monitored by validated and integrated computer systems.

Sequence Scope: Instrument Qualification

On this project, Sequence was responsible for developing a site validation program for the Manufacturing and Laboratory space including laboratory instrument qualification. After the implementation of the new validation program, the project consisted of various system CQV activities for the start-up of the laboratory space. The current lab footprint has expanded resulting in expansion efforts for additional CQV projects.
Client
ElevateBio
Location
Waltham, MA
Cell & Gene Therapy

Life Impact

Analytical Instrument Qualification is the documented collection of activities necessary to establish that an instrument is delivered as designed and specified. All lab instruments should be qualified to demonstrate suitability for the intended use as part of the foundation of all quality analytical work. Instrument qualification is crucial for compliance in the pharmaceutical industry as it ensures regulatory compliance, maintains data integrity, supports quality control, manages risks, and aligns with Good Laboratory Practices. By implementing instrument qualification processes, laboratories can enhance the reliability and credibility of their operations, ultimately contributing to the safety and effectiveness of pharmaceutical products.

By utilizing qualified instruments and retaining the documents required for compliance, cell & gene therapy manufacturing facilities can speed the time to market and ensure that FDA compliance requirements are met.

How can Sequence support your project success?

Equipment Verification Services for Your Project

This site uses cookies for analytical purposes. No user identifiable data is collected or shared. If you agree to our use of cookies, please accept and continue.

Tulip

No Code App Development for Manufacturing Operations

Tulip creates user-friendly and functional apps that improve the productivity of operations, without writing any code. Users can start from scratch or customize an App Template to fit their needs.

Sequence partners with Tulip for implementation and validation of the Tulip platform as well as creation, configuration and validation of Tulip Applications that are hosted on the platform. Our application builds include Electronic Batch Records, Weigh and Dispense, Digital SOPs for training (with embedded videos) and more.