Tailored solutions to drive innovation and integrity, ensuring the success of clinical trials worldwide.
Schedulel a Call
In the fast-paced world of clinical trials, efficient and secure Direct-To/From-Patient deliveries are becoming increasingly important, but complex processes have posed significant logistical challenges.
Meliovit is here to change that.
Our platform is committed to providing tailored solutions that meet the unique needs of each study, ensuring the success and integrity of clinical trials worldwide.
Meliovit offers seamless management of clinical trial logistics, ensuring secure and efficient direct-to-patient delivery and data handling.
With our comprehensive and flexible solution, we aim to deliver exceptional value and utility in a variety of study configurations, including Depot-to-Patient, Site-to-Patient and many other hybrid models.
All new drugs and therapies must be significantly tested before being released to the mass public.
As a clinical trial participant, you get first access to some of the final phases of clinical trials that may improve your health condition or overall quality of life.
As a result, any medications, doctors’ visits, or physical exams are available to you at no cost. There are no bills to pay, no insurance claims.
As a result, any medications, doctors’ visits, or physical exams are available to you at no cost. There are no bills to pay, no insurance claims.
As a result, any medications, doctors’ visits, or physical exams are available to you at no cost. There are no bills to pay, no insurance claims.
Tailored solutions to drive innovation and integrity, ensuring the success of clinical trials worldwide.
The Meliovit mobile app keeps participants informed with shipment updates and delivery tracking on iOS and Android. Designed for ease and accessibility, it ensures continuous engagement throughout the trial journey.
Our desktop application streamlines the clinical trial process for all roles involved. It enables seamless coordination and efficient management of data, supplies, and product delivery.
We understand that each clinical trial has its unique requirements, especially when it comes to the logistics of Direct-To/From-Patient shipments. Meliovit offers extensive customization options to align perfectly with your trial’s specific needs.
Meliovit is designed for quick setup and user-friendly operation, ensuring a seamless integration into your clinical trial processes.
With our comprehensive and flexible solution, we aim to deliver exceptional value and utility in a variety of study configurations, including Depot-to-Patient, Site-to-Patient and many other hybrid models.
Learn More
Our communications are tailored to meet these regulatory requirements, ensuring your outreach is both effective and compliant. By adapting our strategies to different regions, we’re able to reach candidates more effectively than others in the industry.
Learn More
Our flexibility allows for tailored approaches to participant registration and medicinal product dispatching, ensuring the system aligns perfectly with the specific operational needs of each trial.
Learn MoreOur flexibility allows for tailored approaches to participant registration and medicinal product dispatching, ensuring the system aligns perfectly with the specific operational needs of each trial.
Learn MoreEmpowers sponsors and CROs with real-time data for informed
decision-making and efficient trial management.
We prioritize protecting healthcare data, especially in decentralized trials. Committed to security, we strictly adhere to HIPAA and GDPR standards, utilizing advanced encryption for participant confidentiality in Meliovit.
Ensures all sensitive participant contact information is securely stored, maintaining confidentiality and compliance.
Ensures all sensitive participant contact information is securely stored, maintaining confidentiality and compliance.
Ensures all sensitive participant contact information is securely stored, maintaining confidentiality and compliance.
Ensures all sensitive participant contact information is securely stored, maintaining confidentiality and compliance.
Ensures all sensitive participant contact information is securely stored, maintaining confidentiality and compliance.
Ensures all sensitive participant contact information is securely stored, maintaining confidentiality and compliance.
Participants receive alerts about the status of their medicinal product deliveries, including dispatch and expected arrival times.
Notifications for confirming the receipt of deliveries, ensuring investigators and nurses are informed on time.
Prompts for participants to provide feedback on the condition and viability of received packages.
Participants can inform their study staff of any issues that can be handled promptly to prevent unnecessary delays and delivery failures.
Alerts when a new participant is successfully registered via IRT software.
Updates when a shipment request is processed, providing transparency in order management.
Reminders for participants to verify their details, ensuring accurate and up-to-date information.
Notification of delivery success and package viability.
Notifications about upcoming deliveries, or sample returns, enabling nursing staff to prepare for any required assistance.
Immediate alerts when new shipment requests are made, initiating the processing phase.Courier Dispatch Confirmations: updates when couriers are dispatched or when manual courier ordering is required.
Alerts indicating the completion of a shipment’s journey, marking the end of the logistic process for the Hub.
Customizable notifications based on predefined timeout thresholds, such as “Maximum time to delivery”, facilitating immediate alerts if there are delays or issues in the shipment process, enabling quick intervention.
