Präklinische Phase, Phase I & II

Explore OZQA’s collection of SOP templates designed specifically for companies operating in Phase I and Phase II clinical development. These documents support the essential quality processes required for early human studies, including GxP compliance, documentation control, safety reporting, vendor oversight, and data integrity. Each SOP is professionally written and ~95% pre-filled, making it fast and efficient to establish a compliant Quality Management System during early clinical stages — especially for virtual, outsourced, or fast-growing biotech organisations.