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Overcoming Manufacturing Challenges for Ophthalmic Drugs

Preservatives like benzalkonium chloride can irritate the eye, especially with long-term use. Removing them makes manufacturing even more important. Learn how sterile Blow-Fill-Seal (BFS) technology and single-unit packaging help ophthalmic drug developers maintain microbial control without relying on preservatives.
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Strips of single-use plastic unit-dose vials moving through a rotating machine on a pharmaceutical production line, with a cutout of a five-vial Blow-Fill-Seal strip in the corner. Overlay text reads “Overcoming manufacturing challenges for ophthalmic drugs” with the Ritedose logo.

Ritedose Opens Advanced Laboratory and Expands Analytical Capabilities to Accelerate Pharmaceutical Innovation—Positioning the Company as a Preferred Partner for Drug Development and Manufacturing

– Triples laboratory footprint with the $17 million investment. – Features new leachables and extractables testing capabilities. – Allows for seamless development and manufacturing experience while supporting pharmaceutical products throughout entire lifecycle. – Creates an integrated laboratory infrastructure coupled with…
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A smiling scientist in a lab coat, safety glasses, and gloves pours from a reagent bottle into a burette at a laboratory fume hood while a colleague looks on. Overlay text reads "We're investing in the future of pharmaceutical innovation" with the Ritedose logo.

What Ophthalmic Drug Developers Need in a CDMO

Clinical success is only the beginning. For ophthalmic drug developers, the right CDMO can help turn clinical progress into a scalable, sterile, high-quality manufacturing strategy built for commercialization.
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Two cartons of YUVEZZI ophthalmic product moving along a conveyor belt in a pharmaceutical manufacturing facility, with a masked worker in the background. Overlay text reads "What do ophthalmic drug developers need in a CDMO?" with the Ritedose logo.
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