Pharmaceutical and biotech industries must comply with strict regulations to ensure medicines are safe and effective. One key requirement is the Wholesale Distribution Authorisation (WDA) Licence. It is essential for companies distributing medicinal products to ensure they meet rigorous standard…
When computerised systems are identified and their capabilities assessed and challenged, this provides you with assurance that they can be promptly relied upon to give you the data you need, when you need it.
Below is a list of considerations, when you are assessing the suitability for use of …
Majority of deviations raised result from poorly written procedures
Procedures give us direction, structure and consistency in how we perform our daily tasks in ensuring medicines are manufactured and handled with the utmost care.
They are a requirement to comply with our regulations, where …
Computer System Validation (CSV) services ensure data integrity, regulatory compliance and operational efficiency in the pharmaceutical and biotech industries. These sectors require precision and adherence to strict global standards to safeguard product quality and patient safety.
CSV fr…
Precision and reliability in pharmaceutical storage aren’t just desirable. They’re essential. Maintaining proper environmental conditions is critical for preserving product integrity and ensuring patient safety. For pharmaceutical and biotech companies navigating stringent Good Manufactu…
Ensuring product safety, efficacy and regulatory compliance hinges on maintaining the integrity of the pharmaceutical supply chain. GDP Auditing Services (Good Distribution Practice) are crucial in safeguarding this intricate network by mitigating risks and bolstering quality assurance.
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