Quality Commitment
At AdiraMedica, LLC, we are dedicated to providing high-quality clinical trial supplies that meet the rigorous
requirements of clinical research. We strive to ensure that our products and services support the advancement of new
and innovative medicines while maintaining the safety, efficacy, and regulatory compliance required for clinical trials.
We commit to:
Ensuring Compliance with Regulatory Requirements
Adhering to all relevant local and international regulations, including Good Distribution Practice (GDP), Good Manufacturing Practice (GMP), and Good Clinical Practice (GCP), to guarantee that all clinical trial supplies are produced, stored, and distributed in compliance with industry standards.
Providing Safe and Effective Supplies
Delivering clinical trial materials (such as investigational medicinal products, ancillary supplies, and devices) that are safe, high-quality, and suitable for clinical trials, ensuring patient safety and data integrity throughout the trial process.
Timely and Reliable Delivery
Ensuring on-time, accurate, and secure delivery of clinical trial supplies to meet the specific needs of each trial, regardless of location or complexity, while minimizing supply chain risks and delays.
Collaboration with Stakeholders
Collaborating closely with our customers, clinical trial sponsors, and other stakeholders to understand their unique needs, providing customized solutions that enhance the quality and efficiency of clinical trials.
Commitment to Continuous Improvement
Implementing a culture of continuous improvement by monitoring and analyzing our processes, conducting regular training for our team, and incorporating feedback to enhance the quality and reliability of our services.
Risk Management
Identifying and mitigating risks related to clinical trial supplies through proactive planning, ensuring the integrity and stability of the products and minimizing potential disruptions to clinical trials.
Data Integrity and Documentation
Maintaining thorough, accurate, and transparent documentation at every stage of the process, ensuring the traceability and accountability of clinical trial supplies, in accordance with regulatory requirements.
Ethical and Professional Standards
Conducting all aspects of our business with integrity, professionalism, and ethical standards, fostering trust with our clients, partners, and regulatory bodies.
This Quality Policy is communicated to all employees and stakeholders and is reviewed regularly to ensure its
ongoing relevance, effectiveness, and alignment with the evolving needs of the clinical trial industry.
Senior Director, Quality Assurance
