Full preclinical and clinical services

At Al Dana, we specialize in providing comprehensive Toxicology Studies as part of our suite of research services. Our dedicated team of experts works diligently to assess the safety and potential risks of pharmaceuticals, chemicals, and various products to ensure regulatory compliance and safeguard human health.

At Al Dana, we specialize in conducting precise and insightful In Vivo Studies as part of our comprehensive research services. Our dedicated team of scientists and researchers employs cutting-edge methodologies to evaluate the efficacy, safety, and pharmacological profiles of pharmaceuticals, biologics, and medical devices.

At Al Dana, we specialize in conducting comprehensive Safety Studies to ensure the utmost safety and efficacy of pharmaceuticals, biologics, and medical devices. Our dedicated team of scientists, toxicologists, and regulatory experts collaborate closely with clients to design and execute studies that meet stringent regulatory requirements and industry standards.

Al Dana offers a comprehensive suite of Pharmacokinetics (PK) and Bioanalytical Services designed to provide invaluable insights into the behavior of pharmaceutical compounds within biological systems. Our team of skilled scientists, pharmacologists, and analytical experts works collaboratively with clients to design and execute studies that meet regulatory requirements and aid in informed decision-making throughout the drug development process.

At Al Dana, we offer a comprehensive range of Preclinical Services beyond traditional study conduct. Our Consulting and Regulatory Services are designed to provide invaluable support to pharmaceutical, biotechnology, and medical device companies throughout their product development journey. Whether you need expert guidance on study design, regulatory submissions, or strategic planning, our team of seasoned professionals is here to assist you at every stage.

At Al Dana, we specialize in providing comprehensive Clinical Trial Management Services tailored to meet the unique needs of pharmaceutical, biotechnology, and medical device companies. Our experienced team of clinical research professionals is dedicated to ensuring the successful planning, execution, and oversight of clinical trials, from Phase I through Phase IV.

At Al Dana, we offer comprehensive Clinical Data Management Services designed to ensure the accuracy, integrity, and compliance of your clinical trial data. With a focus on efficiency, quality, and regulatory standards, our experienced team of data management professionals ensures that your study data is collected, validated, and analyzed with precision and reliability.

At Al Dana, we offer comprehensive Safety and Pharmacovigilance Services designed to ensure the safety, efficacy, and regulatory compliance of your investigational drugs and medical products throughout their lifecycle. Our dedicated team of pharmacovigilance experts is committed to monitoring, evaluating, and reporting adverse events and safety data with the utmost precision and diligence.

At Al Dana, our Regulatory Services are designed to guide you through the complex landscape of regulatory requirements with confidence and efficiency. We understand the critical importance of compliance with global regulatory standards and the impact it has on the success of your clinical trials and product approvals.

At Al Dana, we offer a comprehensive suite of Clinical Services beyond the traditional scope, designed to enhance the efficiency, quality, and success of your clinical trials. Our Consulting Services and Medical Writing support are tailored to provide valuable insights, strategic guidance, and precise documentation throughout the drug development process.