Our Solutions

We offer end-to-end clinical trial management for Phase I through Phase III studies. Our approach combines regulatory knowledge, operational flexibility, and leadership commitment to deliver high-quality trial outcomes tailored to your project’s unique needs, at a minimum cost.

Our site management team delivers attentive oversight and coordination to ensure your clinical trials run smoothly, from site selection through closeout. We combine local insight with strong project leadership to maintain compliance, optimize resource use, and meet your timelines.

Our elite expertise conducts clinical monitoring emphasizing patient safety, adverse effect management, regulatory compliance, and data accuracy. By proactively identifying and
resolving issues, we support your trial’s success and maintain the highest standards of quality and ethics.

AMZ CRO’s laboratory services are designed to provide timely, accurate analyses tailored to clinical trial needs. In compliance with ISO, GLP and ICH, strong quality management and dedicated lab personnel together ensure reliable results that support confident decision-making.

AMZ CRO’s laboratory services are designed to provide timely, accurate analyses tailored to clinical trial needs. In compliance with ISO, GLP and ICH, strong quality management and dedicated lab personnel together ensure reliable results that support confident decision-making.

Our BA/BE study services combine rigorous protocols, ethical standards, and clinical precision to deliver trustworthy data that meet international regulatory expectations — all within a cost-efficient framework. We along with our reliable partners and expertise are tailoring BE projects with great interest, as a growing regular need of our valuable clients.

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