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Regulatory and Quality Consultancy Support for MedTech, HealthTech and Pharma

CPI needs expert regulatory and quality consultancy to develop and update SOPs and QMS documentation for its MedTech, HealthTech and Pharma portfolio, provide training, and give feedback on project strategy and assumptions.

You'll want to look if you have proven experience in medical device or pharmaceutical regulatory affairs and quality management systems, and can write or update SOPs and QMS documentation.

Umio won a related clinical and laboratory requirements specification consultancy contract in December 2025. Inferred from prior awards to this buyer, not confirmed.

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