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Observation Reports With Redica Systems

Don't get cited by the FDA. Contact us to see if your CDMO sites are adhering to data integrity best practices. But first, don’t forget to download your report.

Download Report Inspection Prep

“It is really amazing what the Redica team has done and where you are going to support the industry… I couldn’t be happier with what I am getting from the platform.”

Director of Process Management and RC, Johnson & Johnson

“This is a powerful analytics tool we use routinely across the full GxP spectrum to monitor supply chain risks, assess vendors, and clinical trial sites. The analytics allow for effective and efficient compliance benchmarking and QMS planning in an easy to use format.”

Vice President, Global Head of Quality, Prothena

“What used to take 2 months now only takes 15 seconds to do in your system.”

Director Compliance and Audit, Medtronic

Insights on Pharma
& Biopharma

Blog

FDA FY2020 Drug Inspection Observations and Trends

Barbara W. Unger
February 4, 2021
Blog

Part I: An Analysis Of MHRA’s Latest Annual GMP Inspection Deficiencies Report

Barbara W. Unger
March 17, 2021
Blog

An Analysis of 2015 to 2019 FDA 483 Data

Rebecca Stauffer
January 28, 2021

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