Data Reporting, Compliance and Integrity – Multimedia

Manage impurity data in pharmaceutical development more effectively in a single informatics solution. Assemble all relevant analytical data with chemical information for real-time access to project information by the entire team.

Download this whitepaper to learn why high data quality and integrity is critical to ensure patient safety and drug efficacy from research and development through to manufacturing.

Data integrity is a fundamental element of ensuring compliance in a regulated laboratory and is not a new concept - it dates back decades.

With computerized laboratory systems now taking the place of paper systems, your compliance strategy must adapt, or you risk difficult regulatory inspections.

This guide highlights 10 important factors that will help you improve your pipetting technique and ensure accurate, reproducible results!

Here are 10 tips to help you optimize your clinical flow cytometry experiments and ensure consistent results.

PerkinElmer Signals Notebook allows you to achieve meaningful scientific breakthroughs – faster, smarter and easier to keep track of your material evidence.

In this case study, learn how a multinational pharmaceutical company has expanded data analytics capabilities for 5000 users, starting with a small group in R&D, to early clinical trials, clinical trial development, safety, regulatory, and more.

This paper outlines the requirements of 21 CFR Part 11 and Annex 11, and provides information on how LabVantage software supports customers in complying with the regulations.

A summary of the Disease Modeling Project for the MODEL-AD consortium.