The current invention relates to an inspection process, particularly for the optical inspection of pharmaceutical products.
Known embodiments of such inspection processes use automatic visual inspection apparatus (AVI) with cameras to detect defects, for example defects in containers or particles within containers. Faulty products can be sorted out to a rejection path. Due to the image quality, the inclusion of bubbles in the liquid in a container or other interferences, a considerable number of products are mistakenly labelled as being faulty. To reduce these numbers, specific features can be used to supply faulty labelled products to a retest path. These products are subsequently checked by a trained inspector or a semi-automatic apparatus, which perform a final pass/fail evaluation. For this, the products to be retested must be supplied to an inspection process, once again. This is time consuming and inefficient.
In the current invention, it is a task to provide an inspection process, with which the above-mentioned drawbacks can be prevented.
This task is solved by a process with the features of claim 1. Further embodiments of the process, as well as an inspection system are defined by the features of further claims.
An inspection process according to the invention comprises the steps of:
For example, the specimen can be an empty container or a container containing a liquid, for example a pharmaceutical container, such as a vial, a bottle, a syringe, an ampoule, a carpule, an infusion bag, an infusion bottle, a BFS-ampoule (blow-fill-seal manufactured), a BFS-bottle, a blister, a tablet blister, an Autoinjector, a Metered-dose inhaler (MDI). All these containers can be made from glass or plastic. The content of such a container can be a fluid, such as a liquid, a gel or a gas. Alternatively, the content may be lyophilized material or a powder or a suspension. The inspection apparatus can comprise an inlet comprising a conveyor, a reading and/or marking unit, an inspection, a sorting unit, a control system, a storage system and an outlet comprising at least one path comprising a conveyor. The identifying can be done before or after the inspecting. The inspecting of the specimen, the assigning of the inspection date, the assigning of a first assessment and the saving to a raw data storage can be done once or can be done repeatedly. For example, a first area of interest can be inspected in one inspection station and a second area of interest can be inspected in another inspection station. Alternatively, if the first inspection produced an ambiguous result, the first inspection can be repeated. It is also possible to have several stages of first inspections, i.e. to have a level one inspection and if the level one inspection is ambiguous, to have a more extensive level two inspection. The area of interest or the region of interest, is defined as the area or region, in which a defect can be expected and thus is inspected. The sorting, based on the first or second assessment, can be done after the inspecting or later and with another inspection apparatus, respective sorting apparatus. The raw data storage, the processed data storage and the result data storage can be different entities, or they can be identical or can be stored on an identical device.
In an embodiment, the first assessment can be selected from the group comprising pass, reject and retest. It is possible to foresee more than one retest assessment. For example, a further assessment could be retest, because there might be an undesired particle in the container or because the container itself comprises an undesired inclusion or has a defect, such as scratches or bumps. In general, intrinsic, extrinsic and inherent defects can be detected and can serve as a basis for the first assessment.
Possible particle inclusions may comprise metal, plastic, fibers, hairs or the like. If no defects have been detected, the specimen receives the assessment pass. If one or more clear defect has been detected, the assessment is reject. It is possible to categorize the defects, such as particle rejection or cosmetic rejection, i.e. cap defects or defects in the side wall or bottom of a container. The assessment can be retest, if, for example, a plurality of inclusions has been detected. In this case, there can be in fact a plurality of inclusions or there can be only air bubbles within the container. Alternatively, if there is an incorrect position correction, i.e. the test window could not be positioned correctly, the assessment is also set to retest. If the tracking of an object doesn't allow for a clear identification, i.e. bubble or particle, the assessment is also set to retest.
In an embodiment, the second assessment can be selected from the group comprising pass, reject and further. Obviously, the second assessment can comprise the same assessments as the first assessment but can also comprise further assessments.
In an embodiment, the first assessment and/or the second assessment comprises a classification. It is possible to classify the defects and use the classification for sorting the specimen. For example, all rejected specimen and/or specimen to be retested can be sorted by classification. The data of the retested specimen, i.e. the data from the second assessment can be used to improve the first assessment. The specimen that received the first assessment pass can also comprise a classification, for example, specimen foreseen for random inspection. The random inspection of good products can be used to guarantee the quality of the assessment process.
In an embodiment, the identifying is done by detecting a provided identification feature on the at least one specimen and/or by applying an identification feature to the at least one specimen. Generally, any identification feature is possible, that allows the individual identification of each specimen.
In an embodiment, the identification feature can be selected from the group comprising alphanumeric code, matrix code, bar code, Inkjet coding, laser coding, electronic coding on a chip. Other identification features such as RFID are also possible.
In an embodiment, the identification feature is an electronic coding on a chip and wherein the chip comprises the raw data storage, the processed data storage and the result data storage. The above-mentioned storages can be part of a single storage or can be part of storages that are separate from one another.
In an embodiment, the inspecting comprises the steps of:
The taking of a picture may comprise the taking of a sequence of pictures, i.e. several pictures or a movie. It is possible to rotate the specimen to be able to take pictures from the specimen from all directions. It is possible to use any means to set inclusions into motion, such as vibration or stimulation by sound.
In an embodiment, the processing comprises the steps of:
Any processing step can be done that simplifies the inspection of the critical areas by a human inspector. For example, in the case the specimen has been rotated during the inspection and pictures have been taken from all directions, the sequence of pictures can be joined to form a flat projection of the surface of the specimen. For example, after each picture, the specimen is rotated by 60 degrees and a total of six pictures is taken to cover a 360 degrees view of the specimen. However, any number of pictures with a corresponding angular rotation of the specimen is possible. It is possible to take more pictures with a smaller image area to obtain a higher resolution of the overall picture. Alternatively, overlapping pictures can be taken to increase the quality of the overall picture.
In an embodiment, the emphasizing is done by marking the critical areas and/or by enlarging the critical areas and/or by increasing the contrast of the critical areas and/or by applying a color filter to the critical areas. In the case, where several pictures have been taken or a movie has been recorded, all static elements can be eliminated by means of a subtraction process, and the moving elements can be highlighted. This is particularly suitable for particle inspection.
The features of the above-mentioned embodiments of the inspection process can be used in any combination, unless they contradict each other.
An inspection system according to the invention comprises
Embodiments of the current invention are described in more detail in the following with reference to the figures. These are for illustrative purposes only and are not to be construed as limiting. It shows
Filing Document | Filing Date | Country | Kind |
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PCT/EP2018/065078 | 6/7/2018 | WO |
Publishing Document | Publishing Date | Country | Kind |
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WO2019/233587 | 12/12/2019 | WO | A |
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Number | Date | Country | |
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20210245203 A1 | Aug 2021 | US |