Welcome to
our Blog
Here you can learn about the latest biometric developments for your sector
Welcome to
our Blog
Here you can learn about the latest biometric developments for your sector
Welcome to
our Blog
Here you can learn about the latest biometric developments for your sector
Ensuring the integrity of data collected in clinical trial EDCs with biometric technology
Ensuring the integrity of data collected in clinical trials is essential and represents a critical step in the introduction of new drugs to the market. The implementation of biometric electronic signatures in Electronic Data Capture (EDCs) ensures their accuracy and reliability.
Audit Trail to ensure data integrity in the pharmaceutical manufacturing process
The biometric electronic signature within the audit trail action log ensures the integrity of records in GMP regulated environments, providing detailed and reliable tracking of recorded activities.
GMP compliance in drug manufacturing
The pharmaceutical industry must ensure compliance with GMP regulations, which include a number of issues, including data integrity. The adoption of biometric technologies, such as iris or fingerprint recognition, emerges as the solution to ensure compliance.
GMP compliance in drug manufacturing
The pharmaceutical industry must ensure compliance with GMP regulations, which include a number of issues, including data integrity. The adoption of biometric technologies, such as iris or fingerprint recognition, emerges as the solution to ensure compliance.
GxP environments and their relevance to the pharmaceutical industry
Within GxP regulated environments, it is essential to ensure data integrity and traceability of actions throughout the supply chain. The adoption of biometric technologies, such as iris or fingerprint recognition, emerges as the solution to ensure compliance.
Consequences of non-compliance with data integrity in the pharmaceutical industry
Non-compliance with GMP regulations, particularly in critical factors such as data integrity and employee identification in manufacturing tasks, can lead to regulatory agencies issuing warning letters and even suspending manufacturing operations. How do you effectively address and prevent these consequences to ensure compliance?
FDA inspections in the pharmaceutical industry
The FDA and EMA share the goal of ensuring compliance with GMP and other applicable regulations in pharmaceutical manufacturing. These entities carry out exhaustive inspections of companies to verify their compliance with established standards. Is your company ready to face the rigorous inspection processes?
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