Atum Medical Research

Site Management

Conducting a clinical study involves numerous aspects, and efficient site management is crucial for the success and integrity of clinical research. At Atum Medical Research, we specialize in providing comprehensive Site Management services to ensure all operational aspects of your study are handled with professionalism and attention to detail.

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Site Feasibility

At Atum Medical Research, our Site Feasibility Service is pivotal in identifying optimal locations for clinical trials. We conduct thorough assessments of potential sites, evaluating factors such as patient demographics, recruitment capabilities, and infrastructure quality. Our rigorous analysis ensures that each site meets regulatory standards and ethical guidelines. By leveraging our expertise, we help sponsors select sites that maximize efficiency and success rates for their clinical studies.

Learn more

Site and Investigator Registration

Our meticulous approach ensures that sites and investigators are registered efficiently and compliantly, adhering to all regulatory requirements. By facilitating this crucial step, we enable our clients to focus on their research objectives with confidence, knowing that their studies are supported by qualified sites and investigators.

Learn more

Regulatory

Our Regulatory Service stands as a steadfast guardian, ensuring meticulous adherence of clinical studies to the prevailing regulations, both on a local and international scale. With unwavering dedication, we undertake the intricate journey through regulatory intricacies, offering steadfast consultancy and unwavering support. Our mission is to meticulously guide our clients, navigating through the labyrinth of regulatory requirements, minimizing hurdles, and expediting essential approvals. Through our comprehensive approach, we not only mitigate delays but also pave the way for swift and efficient regulatory clearance.

Learn more

Assuring ICH GCP and Protocol Compliance

We ensure that every clinical trial we support strictly follows ICH GCP (International Council for Harmonisation – Good Clinical Practice) standards and the approved protocol. Our approach is rooted in ethics, patient safety, and scientific integrity, guaranteeing the credibility and regulatory acceptance of trial outcomes.

Learn more

Budget & Contract Negotiation & Finalization

Our team expertly manages the negotiation and finalization of trial budgets and contracts, balancing the needs of sponsors and investigators. We prioritize transparency, fairness, and speed—ensuring your project starts without delays or miscommunication.

Learn more

Network of Research Sites and Investigators

We maintain a robust network of high-performing research sites and qualified investigators across Romania and beyond. This network enhances trial feasibility, accelerates patient recruitment, and ensures access to specialized expertise across therapeutic areas.

Learn more

Records Management

We manage all trial-related documents and data with precision and confidentiality. From initial trial documentation to final archival, our system ensures full traceability, secure access, and regulatory readiness at every stage of your study.

Learn more

Site Management

Conducting a clinical study involves numerous aspects, and efficient site management is crucial for the success and integrity of clinical research. At Atum Medical Research, we specialize in providing comprehensive Site Management services to ensure all operational aspects of your study are handled with professionalism and attention to detail.

Learn more

Site Feasibility

At Atum Medical Research, our Site Feasibility Service is pivotal in identifying optimal locations for clinical trials. We conduct thorough assessments of potential sites, evaluating factors such as patient demographics, recruitment capabilities, and infrastructure quality. Our rigorous analysis ensures that each site meets regulatory standards and ethical guidelines. By leveraging our expertise, we help sponsors select sites that maximize efficiency and success rates for their clinical studies.

Learn more

Site and Investigator Registration

Our meticulous approach ensures that sites and investigators are registered efficiently and compliantly, adhering to all regulatory requirements. By facilitating this crucial step, we enable our clients to focus on their research objectives with confidence, knowing that their studies are supported by qualified sites and investigators.

Learn more

Regulatory

Our Regulatory Service stands as a steadfast guardian, ensuring meticulous adherence of clinical studies to the prevailing regulations, both on a local and international scale. With unwavering dedication, we undertake the intricate journey through regulatory intricacies, offering steadfast consultancy and unwavering support. Our mission is to meticulously guide our clients, navigating through the labyrinth of regulatory requirements, minimizing hurdles, and expediting essential approvals. Through our comprehensive approach, we not only mitigate delays but also pave the way for swift and efficient regulatory clearance.

Learn more

Assuring ICH GCP and Protocol Compliance

We ensure that every clinical trial we support strictly follows ICH GCP (International Council for Harmonisation – Good Clinical Practice) standards and the approved protocol. Our approach is rooted in ethics, patient safety, and scientific integrity, guaranteeing the credibility and regulatory acceptance of trial outcomes.

Learn more

Budget & Contract Negotiation & Finalization

Our team expertly manages the negotiation and finalization of trial budgets and contracts, balancing the needs of sponsors and investigators. We prioritize transparency, fairness, and speed—ensuring your project starts without delays or miscommunication.

Learn more

Network of Research Sites and Investigators

We maintain a robust network of high-performing research sites and qualified investigators across Romania and beyond. This network enhances trial feasibility, accelerates patient recruitment, and ensures access to specialized expertise across therapeutic areas.

Learn more

Records Management

We manage all trial-related documents and data with precision and confidentiality. From initial trial documentation to final archival, our system ensures full traceability, secure access, and regulatory readiness at every stage of your study.

Learn more

Site Management

Conducting a clinical study involves numerous aspects, and efficient site management is crucial for the success and integrity of clinical research. At Atum Medical Research, we specialize in providing comprehensive Site Management services to ensure all operational aspects of your study are handled with professionalism and attention to detail.

Learn more

Site Feasibility

At Atum Medical Research, our Site Feasibility Service is pivotal in identifying optimal locations for clinical trials. We conduct thorough assessments of potential sites, evaluating factors such as patient demographics, recruitment capabilities, and infrastructure quality. Our rigorous analysis ensures that each site meets regulatory standards and ethical guidelines. By leveraging our expertise, we help sponsors select sites that maximize efficiency and success rates for their clinical studies.

Learn more

Site and Investigator Registration

Our meticulous approach ensures that sites and investigators are registered efficiently and compliantly, adhering to all regulatory requirements. By facilitating this crucial step, we enable our clients to focus on their research objectives with confidence, knowing that their studies are supported by qualified sites and investigators.

Learn more

Regulatory

Our Regulatory Service stands as a steadfast guardian, ensuring meticulous adherence of clinical studies to the prevailing regulations, both on a local and international scale. With unwavering dedication, we undertake the intricate journey through regulatory intricacies, offering steadfast consultancy and unwavering support. Our mission is to meticulously guide our clients, navigating through the labyrinth of regulatory requirements, minimizing hurdles, and expediting essential approvals. Through our comprehensive approach, we not only mitigate delays but also pave the way for swift and efficient regulatory clearance.

Learn more

Assuring ICH GCP and Protocol Compliance

We ensure that every clinical trial we support strictly follows ICH GCP (International Council for Harmonisation – Good Clinical Practice) standards and the approved protocol. Our approach is rooted in ethics, patient safety, and scientific integrity, guaranteeing the credibility and regulatory acceptance of trial outcomes.

Learn more

Budget & Contract Negotiation & Finalization

Our team expertly manages the negotiation and finalization of trial budgets and contracts, balancing the needs of sponsors and investigators. We prioritize transparency, fairness, and speed—ensuring your project starts without delays or miscommunication.

Learn more

Network of Research Sites and Investigators

We maintain a robust network of high-performing research sites and qualified investigators across Romania and beyond. This network enhances trial feasibility, accelerates patient recruitment, and ensures access to specialized expertise across therapeutic areas.

Learn more

Records Management

We manage all trial-related documents and data with precision and confidentiality. From initial trial documentation to final archival, our system ensures full traceability, secure access, and regulatory readiness at every stage of your study.

Learn more