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.
…
Ensuring regulatory compliance is essential in the pharmaceutical and biotechnology industries. These industries deliver safe, effective and high-quality products to patients worldwide.
Adherence to Good Manufacturing Practices (GMP) forms the foundation of this commitment, governin…
Data Integrity is a concept and process that is integral to the business of manufacturing and distribution of medicinal products. It is a practice that must be followed by every employee within the workplace. We learn through our mistakes, and we develop strategies and ways of thinking that i…
We use cookies to improve user experience and analyse website traffic. By clicking “Accept“, you agree to our website's cookie use as described in our Cookie Policy.
