Abstract: The present disclosure provides novel processes for providing sterile, pre-filled syringes or injection devices for pharmaceutical compositions, including protein and biopharmaceutical formulations. In some examples, secondary packaging is performed in an aseptic environment, which removes the need for any terminal sterilization method. In some examples, the aseptic packaging method results in a sterile injection device suitable for use in ophthalmic injections.

Abstract: The present disclosure provides novel processes for providing sterile, pre-filled syringes or injection devices for pharmaceutical compositions, including protein and biopharmaceutical formulations. In some examples, secondary packaging is performed in an aseptic environment, which removes the need for any terminal sterilization method. In some examples, the aseptic packaging method results in a sterile injection device suitable for use in ophthalmic injections.

Abstract: The present disclosure provides novel processes for providing sterile, pre-filled syringes or injection devices for pharmaceutical compositions, including protein and biopharmaceutical formulations. In some examples, secondary packaging is performed in an aseptic environment, which removes the need for any terminal sterilization method. In some examples, the aseptic packaging method results in a sterile injection device suitable for use in ophthalmic injections.

Abstract: An injection device includes a syringe barrel for holding medication, a collar positioned on a proximal end of the syringe barrel, a piston assembly including a piston arranged in the syringe barrel, and a rod member extending through the collar to the piston, and a blocking member arranged on the rod member. The piston assembly is movable distally relative to the syringe barrel in a priming stroke. The piston assembly is movable relative to the collar during the priming stroke of the piston assembly such that the blocking member longitudinally abuts the piston assembly and the collar at an end of the priming stroke of the piston assembly.

Abstract: A hypodermic syringe barrel and needle cannula assembly is provided that is capable of being dry heat sterilized at temperatures of greater than about 250° C. and up to about 350° C. in which the assembly includes a syringe barrel, a needle cannula and a bonding material, where the bonding material is stable above about 250° C., cures to provide a transparent bond, and affixes the needle cannula into the syringe barrel to provide the assembly with a post-sterilization needle pullout strength of at least about 30 newtons.

Abstract: A hypodermic syringe barrel and needle cannula assembly is provided that is capable of being dry heat sterilized at temperatures of greater than about 250° C. and up to about 350° C. in which the assembly includes a syringe barrel, a needle cannula and a bonding material, where the bonding material is stable above about 250° C., cures to provide a transparent bond, and affixes the needle cannula into the syringe barrel to provide the assembly with a post-sterilization needle pullout strength of at least about 30 newtons.