Quality management

Pharmaceutical standards at every process step.

From partner qualification through batch release to GDP-compliant delivery: quality at LIGHV is measurable, documented and auditable.

Our quality commitment

Cultivation and processing partners selected to pharmaceutical criteria — with regular audits and documented releases.

Every batch with a Certificate of Analysis: cannabinoids, terpenes and relevant contaminants before release.

Storage, picking and transport according to Good Distribution Practice — temperature-controlled and traceable.

Batch-related documentation from source to pharmacy delivery for audits and complaints.

Process

Identity check, document review and release only with a complete CoA.

GDP-compliant storage with defined zones, access control and temperature monitoring.

Batch-related picking processes with a four-eyes principle for critical steps.

Documented handover to logistics partners with delivery proof for the pharmacy.

Note: We provide detailed certificates and audit reports within the scope of the business relationship or for approved healthcare professionals.

Our QM team and your professional contacts are happy to help with detailed questions about batches and supporting documents.