Integrity at the heart of your lab
Regulated industries such as food, pharmaceuticals, biologics, cosmetics, and medical devices are now dependent on the ability of scientists to ensure the integrity of their data. Regulators are probing the ways in which data is generated, reported, archived and retrieved. Our OneSource solution is based on centralized monitoring and continual improvements that enable you to pursue science with integrity – and compliance.
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Over the past few years, many regulatory agencies have determined that electronic data is more secure than “paper” documentation and less likely to be manipulated over the phases of a product’s development lifecycle. Printed documentation is no longer considered an exact and complete record since it doesn’t represent the raw data and metadata agencies are looking for. But that doesn’t mean electronic lab data is perfect: It must comply with a number of other stringent regulations, including the US’s 21 CFR Part 11 and the EU’s EDQM Annex 11. The current Good Manufacturing Practice (cGMP) guidelines are an essential tool for laboratories to follow and direct compliance to access controls, lack of permissions, audit trails, backups, and disaster recovery procedures – all of which better enable you to comply with regulators’ expectations for data integrity.
OneSource works with you to assess your data integrity governance program and compliance to ALCOA by reviewing documentation and understanding laboratory systems configurations. From an assessment, a corrective action plan is proposed to give you the roadmap to regaining full compliance in your laboratory. This may include CSV updates or revalidations, and the creation of necessary documentation to satisfy regulatory requirements.
This assessment instills the confidence of compliance and keeps your staff and lab inspection ready.
Scalable services include:
Analytical method requirements that span the full lifecycle — from method development and method transfer to method validation services — can be time-consuming activities. Leverage the OneSource team to streamline lab workflows and boost scientific productivity with data integrity assessment and methods to establish quality control procedures that support reliable research data.
Services include:
Pharmaceutical and life sciences companies now face heightened scrutiny over their practices in documenting their electronic processes in particular, and in managing that data across its entire lifecycle.
The time and resources needed to meet global requirements for regulatory inspections and remaining compliant are at odds with laboratories’ needs to increase productivity and reduce operating costs. Now you can harmonize documentation across all models of lab instruments, regardless of the manufactu ...
“Prove It,” Regulators Say Walter Deming, the legendary physicist and management consultant, once described research this way: “Uncertainty makes research predictable, but you still need proof to satisfy everyone else1.” In one sentence, Deming perfectly describes why compliance management in govern ...
