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Tests and processes that meet EU medical device requirements.
ISO 15189 accredited with GC-MS / LC-MS/MS confirmation.
Sweden, Denmark, Norway, and Finland.
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Seven elements: purpose and legal basis, definitions (drug, alcohol, impairment, working hours), rules and expectations, testing procedures, consequences, confidentiality/GDPR and buy-in (communication and negotiation under the Co-Determination Act (MBL)).