A fire blasting device for manufacturing a medical glass container prevented from breakage and deformation. A glass container is placed on the outer peripheral surface of each of a first roller and a second roller, which are disposed side by side in such a manner that the axis lines are parallel to each other. The axis line of the glass container is parallel to the axis lines of the first roller and the second roller. The entire outer peripheral surface in an inner surface of the glass container corresponding to a region deteriorated by processing is made to abut on the outer peripheral surface of each of the first roller and the second roller. A flame is ejected from a point burner to the region deteriorated by processing in the inner surface of the glass container while rotating the glass container by rotating the first roller and the second roller around the axis lines.

A system for filling multiple sterile containers includes a filter with an inlet port and multiple outlet ports, the outlet ports being pre-attached to sterile containers by respective filling lines of each container. Each container has an interior and each of the respective filling lines are connected to a respective container interior. The respective filling lines are sealed to the outlet ports and the containers such that the container interiors are isolated from an external environment except the inlet port, via the filter, forming a combined interior volume which is sterile. A container that is connectable to an outlet port the system has a bladder, a first tube and a second tube connected to the bladder, and a sterilizing filter. The container, the first tube and the second tube, and the sterilizing filter are sterile before water is flowed through the sterilizing filter into the bladder.

A system for filling multiple sterile containers includes a filter with an inlet port and multiple outlet ports, the outlet ports being pre-attached to sterile containers by respective filling lines of each container. Each container has an interior and each of the respective filling lines are connected to a respective container interior. The respective filling lines are sealed to the outlet ports and the containers such that the container interiors are isolated from an external environment except the inlet port, via the filter, forming a combined interior volume which is sterile. A container that is connectable to an outlet port the system has a bladder, a first tube and a second tube connected to the bladder, and a sterilizing filter. The container, the first tube and the second tube, and the sterilizing filter are sterile before water is flowed through the sterilizing filter into the bladder.

Described herein is a stable oral liquid pharmaceutical product comprising sodium picosulfate, magnesium oxide and citric acid. Particularly, sodium picosulfate is physically separated from magnesium oxide and citric acid prior to dispensing and is mixed at the time of administration.

A system for transferring a sample from a sample recovery or provision device to a microfluidic processing device, more particularly an analysis device, preferably in the form of a flow cell, with a sample carrier that removes the sample from the sample recovery or provision device and can be transported to the processing device. The sample carrier can be connected to the sample recovery or provision device and can be detached from sample recovery or provision device, with the sample being automatically removed. The sample carrier connected to the sample recovery or provision device is preferably a functional component of the sample recovery or provision device, more particularly the sample carrier closes a container space of the sample recovery or provision device for receiving sample material.

A bag assembly that includes a bag portion having first and second walls defining an interior and an opening. The interior is formed by the first and second walls of the bag portion being attached to each other along at least a portion of a perimeter of the bag assembly up to one end of the bag portion. Portions of the first and second walls of the bag portion that are not attached to each other form the opening. The bag assembly also includes an aseptic system for sterile connection and disconnection of the bag assembly from a sterile process, the aseptic system being continuously formed at an interface between the aseptic system and the one end of the bag portion. The aseptic system includes an internal passage to allow fluid communication with the interior of the bag portion and the sterile process.

A bag assembly that includes a bag portion having first and second walls defining an interior and an opening. The interior is formed by the first and second walls of the bag portion being attached to each other along at least a portion of a perimeter of the bag assembly up to one end of the bag portion. Portions of the first and second walls of the bag portion that are not attached to each other form the opening. The bag assembly also includes an aseptic system for sterile connection and disconnection of the bag assembly from a sterile process, the aseptic system being continuously formed at an interface between the aseptic system and the one end of the bag portion. The aseptic system includes an internal passage to allow fluid communication with the interior of the bag portion and the sterile process.

An injection port assembly may comprise a support body having a receptacle associated with a passage through the support body. The receptacle may have at least one recess in an end surface of the receptacle. The receptacle may have a plurality of retainer members. The assembly may further comprise a peripheral rim rib about a periphery of the support body and a number of additional ribs extending from the receptacle to the peripheral rim rib. The assembly may further comprise a delivery assembly coupled within the receptacle via the retainer members. The delivery assembly may have a cannula extending through the passage. The delivery assembly may have an injection receiving volume within the delivery assembly in fluid communication with a lumen of the cannula but otherwise fluidically sealed by a self-sealing barrier. There may be a sole externally accessible portion of the barrier aligned with an axis of the lumen.

An injection port assembly may comprise a support body having a receptacle associated with a passage through the support body. The receptacle may have at least one recess in an end surface of the receptacle. The receptacle may have a plurality of retainer members. The assembly may further comprise a peripheral rim rib about a periphery of the support body and a number of additional ribs extending from the receptacle to the peripheral rim rib. The assembly may further comprise a delivery assembly coupled within the receptacle via the retainer members. The delivery assembly may have a cannula extending through the passage. The delivery assembly may have an injection receiving volume within the delivery assembly in fluid communication with a lumen of the cannula but otherwise fluidically sealed by a self-sealing barrier. There may be a sole externally accessible portion of the barrier aligned with an axis of the lumen.

Disclosed are examples of reservoir and reservoir systems usable with a wearable drug delivery device. An example reservoir may include a flexible component coupled to a shell component. The shell component may include drainage channels to facilitate extraction of the liquid drug from the reservoir. A reservoir system example may include an exoskeleton configured around a flexible reservoir to guide the expansion and collapse of the flexible reservoir. Alternatively, one or more rigid panels may be coupled to corresponding flat surfaces of the flexible reservoir to guide the expansion and collapse of the flexible reservoir. A further reservoir example may include a flexible thin film reservoir having peel-able restraints configured to seal off corresponding sections of the reservoir, sequentially break, enabling the liquid drug to sequentially fill corresponding sections in a controlled and predicable manner. A wearable drug delivery device example suitable for utilizing the described examples is provided.