Disclosed herein is a pierceable elastic septum for use in drug reservoirs and infusion sets, the pierceable septum comprising a first surface and a second surface. The first surface and the second surface are positioned opposite to each other. A distance between the first surface and the second surface is not constant over the first surface, and is configured such that if a higher pressure is applied to the first surface as compared to the second surface, a component of a force, which is exerted on the first surface, acts towards an axis (A) which intersects the center of the first surface and the center of the second surface.

A combination includes: a holding structure including receptacles which are arranged in a regular arrangement and are formed by peripherally formed side walls; containers received in the receptacles, the containers having a basic body which, at an upper end, merges into a shoulder portion which is adjoined by a narrowed neck portion with a widened upper edge with an opening; holding projections provided at lower ends of the receptacles and configured to hold the containers in the receptacles, the holding projections at the lower ends protruding radially inwards into the receptacles, the containers being supported directly on the holding projections; and centering elements provided above the holding projections and configured to center the containers in the receptacles. The centering elements have a beveled configuration and protruding into the receptacles in order to reduce a width of the receptacles at the lower ends thereof in a funnel shape.

A primary packaging container for pharmaceuticals is provided. The container includes a hollow body, an opening, and a closure. The hollow body has an opening and is made of a cycloolefin polymer or a cycloolefin copolymer. The closure has a puncture region. The closure closes the opening with the puncturing region at the opening. The puncturing region is configured to allow introduction of a cannula into the hollow body and resealing the hollow body upon withdraw of the cannula. The closure has an elastomer that is connected to the hollow body so as to be not separable in a non-destructive manner.

A production method for producing a transport and transfer receptacle for at least one fluid medium, for example, for at least one sterile liquid is proposed. The method comprises supplying at least one container for receiving the fluid medium. At least one energy unit is supplied. The energy unit effectsfor example, completeemptying of the fluid medium from the container when the transport and transfer receptacle is used. The fluid medium is introduced into the container and the container is closed. The fluid medium is charged with positive pressure, for example, using the energy unit. The positive pressure is maintained until the fluid medium is removed. Furthermore, a transport and transfer receptacle which can be produced according to the production method and which has at least one packaging is proposed.

A medicine container for medicine substances which can be mixed with one another includes a container body, a stopper and a mixing element. The container body has a first end with a stopper opening and a second end with a base having an outlet. The stopper is displaceable between the ends. A a mixing chamber for receiving the medicine substances is delimited by a portion of an inner casing surface of the container body, a side of the stopper and the base. The mixing element can be disposed in the mixing chamber. The medicine container is adapted to discharge the medicine substances from the medicine container by displacement of the stopper in the direction of the outlet. The stopper is adapted to receive the mixing element at least partially by a recess. The invention further relates to a method for operating such a medicine container.

Methods, assays, compositions and kits for the ligation of short polynucleotides are presented herein. The short polynucleotides are optionally no more than 7 nucleotides in length, and can be as short as 3 or 4 nucleotides in length. The ligation is optionally performed by CV ligase.

An article is described including an article surface and a coating set comprising an optional tie coating or layer, a barrier coating or layer, and a pH protective layer. The respective coatings or layers can be applied by chemical vapor deposition of a polysiloxane or polysilazane precursor in the presence of oxygen. Examples of such an article are a thermoplastic syringe, vial, or blood collection tube with a coated interior portion containing a pharmaceutical preparation or other fluid with a pH of 4 to 8, alternatively 5 to 9. The barrier coating or layer prevents oxygen from penetrating into the thermoplastic syringe, vial, or blood collection tube. The tie coating or layer, if present, and the pH protective coating or layer protect the barrier layer from the contents of the syringe, vial, or blood collection tube.

A fluid reservoir for a fluid infusion device is provided. The fluid reservoir includes a first portion that has a first end and a second end. The first end includes a fluid delivery port and at least one bubble retaining feature adjacent to the fluid delivery port. The fluid reservoir includes a second portion received in the second end of the first portion and movable within the first portion from the first end to the second end. The fluid reservoir defines a fluid chamber between the first portion and the second portion.

Methods and systems for a cartridge assembly for use with an injection system are provided. An example cartridge assembly may include an ampule containing a pharmaceutical product that is sealed at a distal end with a pierceable diaphragm. The cartridge assembly may also include a hub comprising a proximal portion defining a cavity that is configured to engage the distal end of the ampule and a piercing member positioned within the cavity. The piercing member may include a fluid pathway between a proximal end portion comprising an opening and a distal end in fluid communication with a distal opening of the hub. The proximal end portion may engage the pierceable diaphragm, and the piercing member may apply a force to the pierceable diaphragm in the inactivated position without penetrating the pierceable diaphragm.

A system for filling a fluid reservoir of a fluid infusion device with a fluid is provided. The system includes the fluid reservoir having a first portion and a second portion. A fluid chamber is defined between the first portion and the second portion. The second portion is movable within the first portion and includes an interface. The system includes a transfer guard having a first end and a second end. The first end to be coupled to a source of the fluid and the second end having at least one locking member that couples to the interface. The transfer guard defines a fluid flow path for the fluid from the source, and the transfer guard is movable relative to the first portion to fill the fluid chamber with the fluid.