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What is the Correct GMP Date Format?

What is the Correct GMP Date Format?

The confusion caused by failing to use a GMP date format can be frustrating at best, and catastrophic at worst. In this blog, we highlight what can go wrong when regulated industries use inconsistent date formats, and guide you to some information to help you avoid...
How to Describe ‘Good Documentation Practices’

How to Describe ‘Good Documentation Practices’

An easy way to describe Good Documentation Practices (GDP, or GDocP) to a new team member is to ask the question: Would your GMP documents survive the drop test? With data integrity issues increasingly in the spotlight, it’s a good time to recap some of the...
Data integrity and good data governance

Data integrity and good data governance

Data governance and data integrity Companies that excel at using their data as an asset to boost their competitiveness in a global market have recognised that their Quality System (QS) provide more than a regulatory requirement check box and data integrity is key. In...
Defining Data Integrity – ALCOA(+)

Defining Data Integrity – ALCOA(+)

Data Integrity and ALCOA Data Integrity is increasingly becoming a critical GMP issue the in the Pharmaceutical and Medical Device Industry, originally the ALCOA acronym was used as a simple and practical guide by Stan Woolen of US FDA as to the US FDA expectations...