{"id":47451,"date":"2025-11-14T08:34:46","date_gmt":"2025-11-14T07:34:46","guid":{"rendered":"https:\/\/www.swecobelgium.be\/services2\/qualification-and-certification\/"},"modified":"2025-11-14T08:34:46","modified_gmt":"2025-11-14T07:34:46","slug":"qualification-and-certification","status":"publish","type":"services","link":"https:\/\/www.swecobelgium.be\/en\/services\/qualification-and-certification\/","title":{"rendered":"Qualification & Certification"},"content":{"rendered":"
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Safeguard the quality of your pharmaceutical processes with a conclusive approach to qualification<\/h1>\n

In the pharmaceutical industry, a project doesn\u2019t end when it is delivered or commissioned. A rigorous qualification and validation phase follows to ensure compliance with strict quality standards. Sweco guides pharmaceutical clients through this crucial phase, providing specialised support for every part of the so-called V cycle\u2009\u2013\u2009from URS to OQ. It means we can guarantee that each system works as intended and demonstrates compliance with all GMP requirements.<\/p>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t

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Qualification: essential in a regulated sector<\/h3>\n

Unlike other industries, a project in the pharmaceutical industry doesn\u2019t end with its technical delivery. Systems that impact product quality must be qualified in accordance with a strict process. This qualification starts in an early project phase and, together with validation, forms the final step before commissioning.<\/p>\n

All relevant systems are bundled in a Validation Master Plan (VMP)<\/strong>, drawn up in consultation with the client\u2019s quality team. Each system is subsequently subjected to a series of verification processes and tests that make up the V cycle<\/strong>. Sweco supports these processes step by step, providing technical expertise and regulatory knowledge.<\/p>\n

Our support throughout the V cycle<\/h3>\n

Sweco offers specialised support during all steps of the qualification:<\/p>\n