Our Solutions

From Protocol to publication, we offer end-to-end clinical trial management for Phase I to Phase IV 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.

We support seamless liaison with the local Regulatory Authority entitled as Directorate General of Drug Authority (DGDA) to streamline approvals and ongoing regulatory communications.

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.

Our diversified volunteer pool, along with available exposure to the patients from the AMZ Hospital. Ltd. allow us to reach a number of eligible subjects, according to the trial’s need.

Our team drives cutting-edge biomedical research by integrating the latest scientific methodologies and innovative technologies. We focus on generating robust, high-quality data that advances medical knowledge and supports the development of safe and effective therapies.