MP-Connect 5.8 (Security Information Collection_Medical Institutions)
Adverse Event and Side Effect Reporting System (Direct Reporting from Medical Institutions)
A solution to achieve the collaboration of safety information between healthcare professionals and medical representatives.
"MP-Connect" is a web solution that allows healthcare professionals to quickly communicate adverse drug reaction information directly to pharmaceutical companies in the field of drug use (medical institutions, pharmacies, research institutions). When healthcare professionals obtain information about adverse events in a medical setting, they can input the necessary information for the initial report through a web browser, enabling immediate reporting. Pharmaceutical companies operating AE-Connect can view the information reported by healthcare professionals about adverse events on the AE-Connect reception screen, where detailed information can be confirmed. 【Convenient for the following situations】 ■ Secure and easy user registration using an email address is possible. ■ Healthcare professionals do not need to carry a computer or adverse event reporting forms at all times. ■ Adverse event information can be registered with simple operations, so no special training is required. ■ Other files can also be attached to adverse event information. ■ Photos or PDFs taken with devices equipped with camera functions can be attached to adverse event information. ■ Reporting can be done regardless of location. *For more details, please download the PDF or feel free to contact us.
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basic information
【Main Features】 ■User Registration ■Master Reference Input ■Support for Multiple Suspected Drugs and Multiple Event Inputs ■Logical Checks ■Email Notifications ■File Attachments ■PDF Attachments ■Master Registration *For more details, please download the PDF or feel free to contact us.
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【Usage Prerequisites】 To use MP-Connect, user registration and authentication are required. Registration is simple; you need to register the necessary information using your personal email address as your ID, and you will receive an authentication code from MP-Connect for verification. Once you enter the authentication code, your registration is complete. From the next time onward, you will not need to enter the reporter's information, such as the workplace. If you are reporting only this time, you can authenticate using your email address without registering as a user and only submit the adverse event report. Additionally, it is possible to link user information from the pharmaceutical company's healthcare professional site, so please feel free to consult us. *For more details, please download the PDF or feel free to contact us.*
Detailed information
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On the MP-Connect top screen, you can choose whether to register as a user. (Config settings)
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If you provide only safety information without registering as a user on MP-Connect, after reviewing the terms of service, you can enter your email address to receive a verification code, which will allow you to log in. (This applies when registering information only once without user registration on MP-Connect.)
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MP-Connect User Registration Screen (1) (For users who want to register with MP-Connect and use MP-Connect permanently with a user ID and password) After reviewing the terms of service, please enter your user information (including your email address), and a security code will be sent to you.
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MP-Connect User Registration Screen (2) (When registering as a user on MP-Connect and using MP-Connect permanently with a user ID and password) After entering the sent security code, you will change the password of the issued account yourself. You can register as a user of MP-Connect. From then on, you can log in using your email address and account password to use the service.
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Company information
Our company is committed to promoting appropriate IT investments and utilization in businesses by investigating the current situation, including operations, environment, and strategy, and proposing and providing systems that align with the original business, scale, and regulations while suppressing excessive investment in IT. In particular, we focus on the development, sales, and support of software related to the entire process of research and development of pharmaceuticals for the pharmaceutical industry, as well as supporting pharmaceutical development operations and providing consulting for IT implementation, all while offering comprehensive support for systems that comply with the regulations (ministerial ordinances and guidelines) of the Ministry of Health, Labour and Welfare. Please feel free to contact us if you have any inquiries.
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