KR101555666B1 - Radiopharmaceutical ERP System and Apparatus and Method for the same - Google Patents

Abstract

The present invention relates to a radiopharmaceutical ERP system and apparatus and a method for managing the same. A radiopharmaceutical ERP system according to the present invention includes a radiopharmaceutical ERP device and a user terminal. The radiopharmaceutical ERP system manages a drug registration order according to a predetermined time, The radiopharmaceutical ERP system collects the amount of order according to a predetermined time and calculates the total output. The radiopharmaceutical ERP system allocates a center to output according to calculation information and manages a quality test for medicine produced after a production command. The user terminal is connected to the radiopharmaceutical ERP system according to a drug order registration request from a client, receives a user interface for order registration, and displays it on a screen. When the client inputs an order according to a time zone, it can be transmitted to the radiopharmaceutical ERP system.

Description

TECHNICAL FIELD [0001] The present invention relates to an integrated management system for a radiopharmaceutical, and a device and a method for integrated management of a radiopharmaceutical in the system.

The present invention relates to a radiopharmaceutical drug integrated management system, and more particularly, to a radiopharmaceutical drug integrated management system capable of integrally implementing production management, quality control, order management and purchase management suitable for the characteristics (half life) The present invention relates to an integrated management system and method for a radiopharmaceutical drug.

In general, enterprise resource planning (ERP) is an enterprise resource planning (ERP) system that consists of several modules that support the management of key processes such as production, purchasing, inventory, ordering, supplier transactions, Integrated application software package. In other words, as a part of large software that integrally manages the human and material resources of a company, it integrates the processes of each related business such as production management, logistics management and accounting management, Ensure connectivity. In particular, the introduction of the ERP system is a systematic approach that solves problems logically according to a clear principle by dividing the system into units that can manage the entire system to enable a consistent connection between the management and the information system of the enterprise and establish a successful information system Method, i.e., a construction methodology. Recently, ERP suppliers and consulting firms have developed and used their own methods to build enterprise information systems or ERP systems.

These ERP systems have recently been applied to the management of pharmaceuticals in distribution companies or drug companies.

On the other hand, radiopharmaceuticals such as contrast agents are produced and circulated by constructing drug factories in the underground of the hospital because the drug efficacy disappears after a certain period of time. The period during which the drug efficacy is extinguished depends on the content of the radioactive substance, but usually takes about one day (one day), and the radioactive drug that has lost its efficacy is discarded.

Therefore, it is very important to take time to establish the production plan and to distribute the medicine after circulation.

Accordingly, it is urgent to construct a system that can integrate production management, quality control, order management, and purchase management suited to the characteristics (half-life) of radiopharmaceuticals.

Disclosure of Invention Technical Problem [8] Accordingly, the present invention has been made to solve the above-mentioned problems, and it is an object of the present invention to provide a radiopharmaceutical drug integrated management system capable of integrally implementing production management, quality management, order management and purchase management suited to the characteristics (half- The present invention provides an integrated management system and method for a radiopharmaceutical.

To this end, the radiopharmaceutical drug integrated management system according to the embodiment of the present invention manages medicament order registration by predetermined time periods, and when the order is determined by time, the order quantity is aggregated to calculate the total production amount, A radiopharmaceuticals integrated management device that manages quality inspections for finished pharmaceutical products after assigning production orders; A user interface for order registration is displayed and displayed on a screen by accessing the integrated management system of the radiopharmaceuticals according to a request for registering order of medicines from a customer, and when an order for medicines for each time period is inputted through the user interface, Lt; / RTI >

Here, the user interface may include an input area for inputting an order for each predetermined time unit.

An apparatus for integrated management of radiopharmaceuticals according to an embodiment of the present invention includes a communication unit for performing data transmission / reception with a user terminal; A controller for receiving drug orders from the user terminal through the communication unit on a time slot basis, instructing production by allocating a production amount for each production center based on an order registration time zone, performing a quality test on the produced drug product, and managing the test results .

Here, the control unit may include: a sales management unit managing medication order registration by a preset time period and registering a medication order by time from the user terminal through the communication unit; A production management unit for calculating the total production amount by counting the order quantity when the order for each time period is determined and for instructing the production by allocating the production amount per center according to the calculation information; And a quality control unit for carrying out a quality inspection for the finished drug product and managing the drug delivery and result information according to the inspection result.

The production management unit may perform a production simulation so as to determine the most efficient production start time and the possible quantity by selecting a production time for an order for each time period considering a half-life period for production schedule management for each order delivery time period.

The production management unit can find optimal production conditions while changing the time zone, and can simulate a large number of productions so as to procure at the correct time.

The production management unit may simulate production so as to minimize the operation of a pharmaceutical production machine such as a sercyclotron (particle accelerator) on the basis of the total amount of several orders at the same time.

The production management unit may allocate a production amount to each center by each order unit based on the production simulation data.

The apparatus for integrated management of radiopharmaceuticals further includes an output unit for displaying data. The production management unit allocates an order to each center, recognizes the facility availability time for each center, Disable message through the output unit.

In order to prevent the production management unit from being driven to one center on a specific day, the production management unit may manage to adjust the total allocated amount in consideration of the backup center, if necessary.

The quality management unit may manage the test results such as a pre-test (TEST) and a post-test (TEST) to suit the characteristics of the radiopharmaceuticals, and to register results after inputting each test item as reference information.

The quality management unit may manage to input a test result over time by adding a test item non-standard time (TIME) criterion.

A method for integrated management of radiopharmaceuticals according to an embodiment of the present invention includes: registering a drug order by time from a customer; Calculating a total production amount by counting the order quantity when the order for each time period is confirmed, and allocating a production amount per center according to the calculation information; Directing production of the medicines allocated to each center; And performing a quality inspection on the finished drug product.

Here, in the step of allocating the production amount, a production simulation is performed so as to determine the most efficient production start time and a possible amount by selecting a production time for a time-based order considering a half- Can be used to allocate production.

The step of allocating the production amount may allocate the production amount using a plurality of production simulations so as to find the optimal production conditions while changing the time zone and to procure the correct time.

The step of allocating the production amount may be to allocate the production amount using production simulation so as to minimize the operation of the pharmaceutical production machine such as a sercyclotron (particle accelerator) based on the total amount of the plurality of orders at the same time .

The step of allocating the production amount may allocate the production amount per time unit to each center according to each order unit based on the production simulation data.

The method for integrated management of radiopharmaceuticals may further include allocating an order to each center after the step of allocating the production amount and outputting an automatic allocation unavailable message if it is impossible to recognize the facility availability time for each center .

In the step of allocating the production amount, it is possible to allocate the total amount of allocations by considering the backup center, if necessary, in order to prevent it from being pushed to one center on a specific day.

The step of performing the quality inspection may include a step of performing a pre-test (TEST) and a post-test (TEST) so as to match the characteristics of the radiopharmaceuticals, and a step of registering results after inputting each test item as reference information .

The step of performing the quality inspection may include a step of adding a test item non-standard time (TIME) criterion so as to input test results according to time.

According to the present invention, by taking into account the half-life period of the radiopharmaceutical, time-based order entry can be performed, thereby enabling production to be carried out in accordance with the order of the customer's required time period.

In addition, considering the half-life of radiopharmaceuticals, it is possible to plan the production by order delivery time, so that it is possible to procure medicines at the right time with optimal production conditions.

In addition, since the production amount can be assigned to each center in consideration of the half-life of the radiopharmaceutical, the production can be more effectively performed.

In addition, quality control can be implemented integrally by making it possible to set test items and test periods according to radiopharmaceuticals quality control characteristics.

BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a block diagram of an integrated management system for radiopharmaceuticals according to an embodiment of the present invention; FIG.
2 is a detailed block diagram of an integrated management system for radiopharmaceuticals according to an embodiment of the present invention.
FIG. 3 is a flowchart illustrating a process for administering a pharmaceutical product according to an embodiment of the present invention. FIG.
FIG. 4 is a flowchart illustrating a process for producing and managing pharmaceuticals according to an embodiment of the present invention. FIG.
5 is a flowchart illustrating a process for medicament quality control according to an embodiment of the present invention.
FIG. 6 is an exemplary diagram for explaining the flow of integrated management of radiopharmaceuticals according to an embodiment of the present invention; FIG.
FIG. 7 is an exemplary view showing a drug sales management screen according to an embodiment of the present invention; FIG.
FIG. 8 and FIG. 9 are diagrams illustrating screen examples of a drug production management screen according to an embodiment of the present invention; FIG.
FIG. 10 is an exemplary screen showing a drug quality control screen according to an embodiment of the present invention. FIG.

Hereinafter, preferred embodiments of the present invention will be described in detail with reference to the accompanying drawings. In the following description and the accompanying drawings, detailed description of well-known functions or constructions that may obscure the subject matter of the present invention will be omitted. It should be noted that the same constituent elements are denoted by the same reference numerals as possible throughout the drawings.

The terms and words used in the present specification and claims should not be construed to be limited to ordinary or dictionary meanings and the inventor is not limited to the concept of terminology for describing his or her invention in the best way. It should be interpreted as meaning and concept consistent with the technical idea of the present invention. Therefore, the embodiments described in the present specification and the configurations shown in the drawings are merely the most preferred embodiments of the present invention, and not all of the technical ideas of the present invention are described. Therefore, It is to be understood that equivalents and modifications are possible.

First of all, referring to FIG. 6 regarding the flow of the radiopharmaceutical administration management, the user receives registration 10 of order from a company (a customer) who requires a pharmaceutical such as a hospital.

When the order is registered, sales / distribution management such as order confirmation 20, delivery management 21, delivery 22, transaction specification management 23, and business analysis management 24 is performed.

Thereafter, the order quantity / purchase request 30, the production quantity allocation 31, the production / distribution request 32, the production record management 33, the production record approval 34, the production completion 35, Production / quality control such as approval (36) takes place.

Next, purchase / material management such as quotation management 40, purchase order 41, approval 42, material receipt 43, import inspection 44, material input 45 and inventory management 46 .

Finally, the supplier will submit a quotation (50) and a delivery (51).

A method for integrally managing production planning and distribution management functions in the business flow for managing such radiopharmaceuticals will be described in detail below.

Now, a configuration of the integrated radiopharmaceutical management system according to an embodiment of the present invention will be described with reference to FIG.

1 is a configuration diagram of a radiopharmaceuticals integrated management system according to an embodiment of the present invention.

1, the integrated system for managing radiopharmaceuticals according to the present invention may include at least one user terminal 100, a radiopharmaceutical integrated management device 120, and a database (DB) 130.

The user terminal 100 is a terminal capable of communicating with the radiopharmaceutical drug integrated management device 120 and capable of transmitting and receiving various data. The user terminal 100 may be a tablet PC, a laptop, a personal computer (PC), a smart phone, a personal digital assistant (PDA), a smart TV, A mobile communication terminal, or the like. In particular, the user terminal 100 according to the present invention can order and register a radiopharmaceutical through communication with the radiopharmaceutical drug integrated management device 120.

In particular, when the user terminal 100 according to the present invention accesses the radiopharmaceuticals integrated management device 120 according to a customer's request for registering a radiopharmaceuticals order, the user terminal 100 provides a user interface for order registration from the radiopharmaceuticals integrated management device 120 Receive.

Here, the user interface may be a screen displayed on a display window of the user terminal 100. A screen for registering an order can be shown in Fig. Referring to FIG. 7, in order to proceed with production by inputting the order of the customer's required time by the phenomenon that the drug efficacy is halved over time due to the characteristic of the radiopharmaceutical drug like 700, Lt; / RTI > In the embodiment of the present invention, the time unit is divided into 30 minutes and 15 minutes for the user to select. However, the time unit setting may be design changeable.

The radiopharmaceutical drug integrated management device 120 is an apparatus for providing integrated management suited to the characteristics of a radiopharmaceutical drug, and integrally manages production management, quality management, order management, and purchase management.

The radiopharmaceutical drug integrated management device 120 performs sales management, production management, and quality management according to the registered order, when the radioactive medicine order registration is requested from the user terminal 100. The configuration of the radiopharmaceutical drug integrated management device 120 according to an embodiment of the present invention will be described in detail with reference to FIG.

2 is a detailed configuration diagram of a radiopharmaceutical drug integrated management apparatus according to an embodiment of the present invention.

2, the radiopharmaceutical drug integrated management device 120 may include a control unit 200, a communication unit 210, an input unit 220, and an output unit 230.

First, the control unit 200 performs overall control of the radiopharmaceutical drug integrated management device 120.

The control unit 200 may include a sales management unit 201, a production management unit 202, and a quality management unit 203 to more effectively perform the functions of the integrated radiopharmaceutical drug management device 120. [

The sales management unit 201 manages the order entry and the order registration by time in consideration of the characteristics (half-life period) of the radiopharmaceuticals.

The sales management unit 201 provides an order screen to the user terminal 100 when there is a request for ordering a radiopharmaceutical from the user terminal 100. At this time, the sales management unit 201 includes an input area for entering an order for each time unit at the time of order registration and payment so that the order can be inputted by the customer in the order screen. At this time, it is preferable that the time unit is divided into 30 minutes and 15 minutes so as to be selected by the user, but the time unit setting may be a design changeable matter. In addition, an order screen can be shown as shown in FIG. 7, and an input area in which an order for each time unit can be input can be included in the order screen as 700.

In addition, when the customer requests the order by wire instead of registering the order directly by the customer through the user terminal 100, the manager inputs the order by time slot requested by the customer through the order screen provided by the sales management unit 201 And may perform order registration.

When the order registration is completed in this manner, the sales management unit 201 confirms the order by time zone, and proceeds to produce the corresponding radiopharmaceuticals by the determined time zone.

The production management unit 202 manages the production schedule for each order delivery time considering the characteristics (half-life period) of the radiopharmaceuticals and manages allocation of the production amount for each center considering the characteristics (half-life period) of the radiopharmaceuticals.

First, in order to manage the production schedule by order delivery time, the production management unit 202 selects a production time for a time-based order considering a half-life period, and simulates production so that the most efficient production start time and possible quantity can be determined. In addition, the production management unit 202 finds optimal production conditions while changing the time zone, and simulates a plurality of productions to be procured at the correct time. In addition, the production management unit 202 simulates production so as to minimize the operation of the drug producing machine such as a syringotron (particle accelerator) on the basis of the total amount of several orders at the same time. The management screen that is thus aggregated in the order quantity can be shown in Fig.

Next, in order to manage production allocation by center, the production management unit 202 allocates a production amount to each center by each order unit based on the production simulation data. In addition, the production management unit 202 allocates an order to each center, recognizes the facility availability time for each center, and outputs an automatic allocation disable message through the output unit 230 when the addition is impossible. In addition, the production management unit 202 manages the allocation to be adjusted in consideration of a backup center in order to prevent it from being pushed to one center on a specific day. At this time, the production amount management screen for each center can be shown as shown in FIG.

Returning to FIG. 2, the quality management unit 203 manages the test items and the test period according to characteristics of the radiopharmaceuticals quality management.

The quality management unit 203 manages the test results such as a pre-test and a post-test to suit the characteristics of the radiopharmaceutical, and registers the results after inputting each test item as reference information. In addition, the quality control unit 203 manages the input of test results over time by adding a test item out-of-standard time (TIME) criterion. Such a management screen can be shown in FIG. 10, and in FIG. 10, 1000 is an area indicating a time reference, and each test item can be input as reference information.

The communication unit 210 performs a function for transmitting and receiving data to and from the user terminal 100 via the communication network 110. Here, the communication unit 210 includes RF transmitting means for up-converting and amplifying the frequency of the transmitted signal, RF receiving means for low-noise amplifying the received signal and down-converting the frequency. The communication unit 210 may include at least one of a wireless communication module (not shown) and a wired communication module (not shown). When the user terminal 100 uses wireless communication, the wireless communication module uses any one of a wireless network communication module, a wireless LAN communication module, and a wireless LAN communication module in order to transmit and receive data according to a wireless communication method. And transmit and receive data to and from the radiopharmaceutical drug integrated management device 120. The wired communication module is for transmitting / receiving data by wire. The wired communication module may connect to the communication network 110 through a wired line and transmit / receive data to / from the radiopharmaceuticals integrated management device 120.

The input unit 220 receives various information such as numbers and character information and transmits a signal input from the manager in association with the administration of the radiopharmaceuticals to the control unit 200.

The output unit 230 displays information on a series of operation states, operation results, and the like that occur during the management of the radiopharmaceuticals. The output unit 230 may be a liquid crystal display (LCD), a thin film transistor LCD (TFT-LCD), a light emitting diode (LED), an organic light emitting diode (OLED) An organic light emitting diode (OLED), an organic light emitting diode (OLED), a retina display, a flexible display, and a three-dimensional display.

The database (DB) 130 is a device for storing data, and includes a main storage device and an auxiliary storage device. The database (DB) 130 stores application programs necessary for the functional operation of the radiopharmaceutical integrated management device 120 and data / RTI > The DB 130 may be provided separately from the radiopharmaceutical drug integrated management device 120 as shown in FIG. 1, but may be included in the radiopharmaceutical drug integrated management device 120.

The communication network 110 performs a series of data transmission and reception operations for data transmission and information exchange between the user terminal 100 and the radiopharmaceuticals integrated management apparatus 120. In particular, the communication network 110 may use various types of communication networks and may be, for example, a wireless LAN (WLAN), a Wi-Fi, a Wibro, a WiMAX, HSDPA, and High Speed Downlink Packet Access) or a wireless communication method such as Ethernet, xDSL (ADSL, VDSL), Hybrid Fiber Coax (HFC), Fiber to the Curb (FTTC) A wired communication method can be used. Meanwhile, the communication network 110 is not limited to the above-described communication method, and may include any other known or later-developed communication methods in addition to the communication methods described above.

A method for integrally managing the radiopharmaceuticals in the radiopharmaceuticals integrated management device 120 configured as described above will now be described with reference to FIGS. 3 to 5. FIG.

First, referring to FIG. 3, a process for medicines sales management will be described.

3 is a flowchart illustrating a process for administering a pharmaceutical product according to an embodiment of the present invention.

The radiopharmaceutical drug integrated management device 120 provides an order screen to the user terminal 100 that can be ordered according to a request for ordering a radiopharmaceutical from the user terminal 100 and selects a specific checkout time zone from the user terminal 100 , The order is confirmed at the selected examination time slot (S300 to S302).

Then, the radiopharmaceutical drug integrated management device 120 starts production of the radiopharmaceuticals based on the determined inspection time slot (S304).

Next, the process for medicines production management will be described with reference to FIG.

4 is a flowchart illustrating a process for producing and managing a drug product according to an embodiment of the present invention.

When the order is closed after the order for the period of examination is confirmed through the process as shown in FIG. 3, the radiopharmaceutical drug integrated management device 120 counts the order quantity (S400).

The radiopharmaceutical drug integrated management device 120 calculates the total production amount (S402).

Thereafter, the radiopharmaceutical drug integrated management device 120 allocates a production amount for each center (S404). At this time, the radiopharmaceutical drug integrated management device 120 selects a production function time for a time-based order considering half-life for management of a production schedule by an order delivery time period, and performs production simulation Simulation is performed to find the optimal production conditions while changing the time zone and to procure the exact time. In addition, the production simulation is performed so as to minimize the operation of the pharmaceutical production machine such as the siclocrotron (particle accelerator) based on the total amount of the plurality of orders at the same time. The radiopharmaceutical drug integrated management device 120 allocates a production amount to each center in each order unit on the basis of the production simulated data as described above.

In addition, the radiopharmaceutical drug integrated management device 120 allocates an order to each center, recognizes the facility availability time for each center, and outputs an automatic allocation disable message if it is impossible to add. Also, in order to prevent it from being pushed to one center on a specific day, it is managed to adjust the total amount of allocation considering backup center when necessary. To this end, the radiopharmaceutical drug integrated management device 120 calculates a total production amount by inputting a production end time for each center in consideration of a backup available center. If necessary, the second production end time may be allocated.

Finally, the process for medicament quality control will be described with reference to FIG.

5 is a flowchart illustrating a process for medicament quality control according to an embodiment of the present invention.

4, the radiopharmaceutical drug integrated management device 120 performs a quality check on the radiopharmaceutical produced through each center (S500 to S502).

If the quality inspection result is affirmative, the radiopharmaceutical drug integrated management device 120 manages the production results and delivers the produced radiopharmaceuticals (S504 to S508). That is, the radiopharmaceutical drug integrated management device 120 registers the results after pre-test (TEST) and post-test (TEST) and each test item are input as reference information in accordance with the characteristics of the radiopharmaceuticals. In addition, the quality management unit 203 adds a test item out-of-standard time (TIME) criterion to input test results over time.

However, if the result of the quality check is rejected, the radiopharmaceutical drug integrated management device 120 discards the radiopharmaceuticals (S506).

The method for the integrated management of radiopharmaceuticals according to the present invention may be implemented in a form of software readable by various computer means and recorded in a computer-readable recording medium. Here, the recording medium may include program commands, data files, data structures, and the like, alone or in combination. Program instructions to be recorded on a recording medium may be those specially designed and constructed for the present invention or may be available to those skilled in the art of computer software. For example, the recording medium may be an optical recording medium such as a magnetic medium such as a hard disk, a floppy disk and a magnetic tape, a compact disk read only memory (CD-ROM), a digital video disk (DVD) Includes a hardware device that is specially configured to store and execute program instructions such as a magneto-optical medium such as a floppy disk and a ROM, a random access memory (RAM), a flash memory, do. Examples of program instructions may include machine language code such as those generated by a compiler, as well as high-level language code that may be executed by a computer using an interpreter or the like. Such hardware devices may be configured to operate as one or more software modules to perform the operations of the present invention, and vice versa.

The foregoing description is merely illustrative of the present invention, and various modifications may be made by those skilled in the art without departing from the spirit of the present invention. Accordingly, the embodiments disclosed in the specification of the present invention are not intended to limit the present invention. The scope of the present invention should be construed according to the following claims, and all the techniques within the scope of equivalents should be construed as being included in the scope of the present invention.

100: user terminal 110:
120: Radiological drug integrated management device 130: Database (DB)
200: control unit 210: communication unit
220: input unit 230: output unit
201: production management unit 202: quality management unit
203: order management unit 204: purchase management unit

Claims (15)

When the order is determined by time zone, the order quantity is totaled and the total production quantity is calculated. The production quantity is assigned according to the production information, and the production is ordered. Managing integrated radiopharmaceuticals;
A user interface for order registration is displayed and displayed on a screen by accessing the integrated management system of the radiopharmaceuticals according to a request for registering order of medicines from a customer, and when an order for medicines for each time period is inputted through the user interface, To the user terminal,
The integrated radiopharmaceutical administration device includes:
When the order for the time period is confirmed, the production conditions suitable for the half-life of the drug are found while changing the production time available for each center, and a plurality of production simulations are performed so as to procure the exact time, and based on the production simulated data, And a production amount per hour is allocated to the radioactive pharmaceuticals.
The method according to claim 1,
Wherein the user interface comprises:
And an input area for inputting an order for each predetermined time unit.
A communication unit for performing data transmission / reception with the user terminal;
A control unit for registering drug orders from the user terminal through the communication unit on a time slot basis, designating production by allocating a production amount for each production center on the basis of an order registration time zone, performing a quality check on the produced drug, Lt; / RTI >
Wherein,
A sales management unit for managing medication order registration by a predetermined time slot and registering a medication order by time from the user terminal through the communication unit;
A production management unit for calculating the total production amount by counting the order quantity when the order for each time period is determined and for instructing the production by allocating the production amount per center according to the calculation information; And
And a quality control unit for carrying out a quality inspection for the finished pharmaceutical product and managing the dispensing and result information of the medicine according to the inspection result,
The production management unit,
When the order for the time period is confirmed, the production conditions suitable for the half-life of the drug are found while changing the production time available for each center, and a plurality of production simulations are performed so as to procure the exact time, and based on the production simulated data, And allocating a production amount by time zone.
delete The method of claim 3,
The production management unit,
A production time is selected for a time-based order considering the half-life of the medicines in order to manage the production schedule for each order delivery time, and the production simulation is performed so that the most efficient production start time and the possible amount can be judged. Device for integrated management.
delete The method of claim 3,
The production management unit,
Characterized in that the production simulation is performed so as to minimize the operation of the pharmaceutical production machine such as a syringotron (particle accelerator) based on the total amount of the plurality of orders at the same time.
delete The method of claim 3,
Further comprising an output section for displaying data,
The production management unit,
Wherein the order is assigned to each center, and when it is not possible to recognize the facility availability time of each center, an automatic allocation unavailable message is output through the output unit.
The method of claim 3,
The production management unit,
Wherein the total amount of the administration is controlled in consideration of a backup center, if necessary, in order to prevent the patient from being driven to one center on a specific day.
The method of claim 3,
Wherein the quality management unit comprises:
Wherein the information is managed so as to register preliminary test (TEST) and post test (TEST) according to the characteristics of the radiopharmaceutical, and inputting each test item as reference information and registering the result.
The method of claim 3,
Wherein the quality management unit comprises:
(TIME) criterion is added to manage the input of test results according to the passage of time. ≪ RTI ID = 0.0 > 8. < / RTI >
Registering a drug order by time zone from a customer;
Calculating a total production amount by counting the order quantity when the order for each time period is confirmed, and allocating a production amount per center according to the calculation information;
Directing production of the medicines allocated to each center; And
And performing a quality inspection on the finished drug product,
The step of allocating the production amount includes:
When the order for the time period is confirmed, the production conditions suitable for the half-life of the drug are found while changing the production time available for each center, and a plurality of production simulations are performed so as to procure the exact time, and based on the production simulated data, And assigning a production amount by time zone.
14. The method of claim 13,
The step of allocating the production amount includes:
In order to manage the production schedule by the order delivery time, the production time is selected for the time-based order considering the half-life period, and the production amount is allocated using the production simulation so as to determine the most efficient production start time and the possible amount Methods for Integrated Management of Radiopharmaceuticals.
14. The method of claim 13,
Wherein performing the quality inspection comprises:
The method comprising the steps of: pre-testing (TEST) and post-testing (TEST) to suit the characteristics of the radiopharmaceutical, and managing the test results so that they can be registered after inputting each test item as reference information .

Images