The present invention is concerned with a sterile aqueous ophthalmic solution comprising about 0.05% to about 0.5% (w/w) of N—(N-acetylcysteinyl-)chitosan or a pharmaceutically acceptable salt thereof in a carrier solution, wherein the N—(N-acetylcysteinyl-)chitosan has a content of free thiol groups in an amount of from 80 μmol/g polymer to 280 μmol/g polymer. The invention is also concerned with a container containing said ophthalmic solution as well as the use thereof in the prevention or treatment of dry eye syndrome or dry eye signs and/or symptoms.

This invention provides a method of treating a subject afflicted with a neurodegenerative disease comprising periodic administration of an amount of laquinimod and an amount of fingolimod, wherein the amounts when taken together are effective to treat the subject. Also provided are packages and pharmaceutical compositions comprising laquinimod and fingolimod for treating a subject afflicted with a neurodegenerative disease. Also provided is a pharmaceutical composition comprising laquinimod for use as an add-on therapy or in combination with fingolimod, and a pharmaceutical composition comprising fingolimod for use as an add-on therapy or in combination with laquinimod, for treating said subject.

A dehumidifying device for a housing, in particular an electronics housing of an electromotor with a dehumidifying chamber includes a wall inside of which a hygroscopic material is received which is designed to bind air moisture from the dehumidifying chamber. The wall of the dehumidifying chamber includes at least one inner membrane permeable to vapor which can be brought into an active connection with an inner receiving space of the housing and an outer membrane which can be brought into an active connection with the outside environment of the housing. The at least one inner membrane and the outer membrane are permeable to vapor at least in a direction in which a transport of air moisture out of the inner receiving space of the housing through the dehumidifying chamber into an outside environment can be ensured.

A medical sterile packaging unit for a sterile-packaged medical product, in particular for a filter module, including a primary packaging with at least one sterile-packaged and hermetically sealed medical product inside it, at least one nestable tray, with a plurality of inserts for each of the medical products packaged in the primary packaging, and at least one sleeve which wraps around the at least one tray with the primary-packaged medical products contained in it.

A sterile packaging unit of a medical filter module including a filter module packed in a sterile primary package, wherein the primary package is a blister package including a molded part having a receiving compartment for the filter module and a cover part arranged on the molded part and hermetically sealing the receiving compartment, wherein the primary package includes a getter for binding molecular oxygen present in the receiving compartment and the filter module is mounted by form closure with respect to the molded part.

A sterile filter module/dialyzer packaging including a filter module, preferably a dialyzer, sterile-packaged in a primary packaging. The filter module having an essentially cylindrical central section and a filter module connection formed at the end of the central section. The primary packaging is a blister packaging with a plastic molded part as a lower section forming a receiving compartment for the filter module and a soft upper foil which, with the lower section, closes the receiving compartment for the filter module. The upper foil is fixed onto the lower section so as to be hermetically sealed and the filter module is fixed at least in sections by means of form fit.

A food preservation system can include a gas (e.g., oxygen) permeable package having at least one oxygen permeable member defining a package chamber therein, and a silverized biomass in the package chamber of the oxygen permeable package. Another food preservation system can include a container having an internal chamber, and an oxygen permeable divider located in the internal chamber so as to divide the internal chamber into a first chamber and a second chamber. The first chamber can being configured for receiving food therein, and a silverized biomass is located in the second chamber. A method of preserving food can include retaining a food in a container that includes silverized biomass such that the food does not contact the silverized biomass. The silverized biomass can have a combination of silver and biomass.

A substantially moisture tight container and lid assembly for storing and packaging moisture-sensitive items comprising an assembly with a container and a lid, the lid is attached by a hinge to an upper housing portion of the container, the lid includes a lip seal member that depends downwardly from the lid, the lip seal member is configured to abut at least a portion of the interior side of the container when the lid is in the closed position resulting in a substantially moisture tight seal between the lid and the lid, and the container assembly further comprising a base portion and an upper housing portion, the upper housing portion is capable of being snap-fit into the base portion by employing a lip seal mechanism to form a substantially moisture-tight seal.

An assembly for receiving fluid pharmaceutical waste into a fluid waste receiver includes a fluid receiver body coupled to a fluid receiver cap, and receiving solid pharmaceutical waste into a solid waste receiver includes a solid receiver body coupled to a solid receiver cap. The assembly comprises a receiver housing and a receiver lid coupled to the receiver housing. The receiver housing comprises a retainer base, sidewalls extending from the retainer base, and dividers extending from the sidewalls to divide an interior of the receiver housing into a receiver compartment configured to receive the fluid receiver body and the solid receiver body, and a cap compartment. A first of the dividers divides the receiver compartment from a first of the cap compartments configured to receive the fluid receiver cap, and a second one of the dividers divides the receiver compartment from a second of the cap compartments configured to receive the solid receiver cap.

A device on which to place contact lens case components to dry. The device is a mat with drainage channels formed thereon. The contact lens components are placed on spaced-apart walls that define the drainage channels and the spaced-apart wall receive the contact lens components and hold them above the drainage channels. This arrangement allows liquid solution and residue to drain from the contact lens case components place on the mat. The mat is sloped and the liquid solution flows to a lip on one end of the mat and then off of the mat. The mat has a slightly sloped base to assist in such drainage.