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Sterility and Accountability in Ophthalmic Manufacturing of Eye Drops
Eye drops and other ophthalmic preparations are used [...]
Risks and Rewards Associated with Developing Lyophilized Vials
For transporting, storing, and handling drugs and other [...]
Properties Affecting Homogeneity in Semi Solid Manufacturing
Semi solids such as creams, lotions, gels, and [...]
Reducing Contamination in Parenteral Manufacturing
Emphasizing quality and compliance through every step of [...]
Manufacturing of Capsules Requires Formulation Adaptations
APIs, excipients, capsule materials and production methods should [...]
Crucial Steps For Obtaining Medical Device Regulatory Compliance
By aligning the many interlocking parts of the [...]
5 Key Challenges in Medical Device Preclinical Testing
The engineering of a medical device constitutes only [...]
On-Going Research
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The Pros and Cons of Closed-Vial Technology in Sterile Vial Filling
The increasing demand for parenteral products delivered in vials brings with in an increased demand for sterile vial filling — can closed-vial technology help manufacturers keep up? By the year 2021, the global market share [...]
Sterility and Accountability in Ophthalmic Manufacturing of Eye Drops
Eye drops and other ophthalmic preparations are used by millions of individuals all over the world; in order to keep them safe and guarantee effectiveness, maintaining sterility is vital to proper ophthalmic manufacturing. Ophthalmic manufacturing; [...]
Risks and Rewards Associated with Developing Lyophilized Vials
For transporting, storing, and handling drugs and other parenteral products that are unstable in solution, lyophilized vials remain the go-to solution for 80% of the industry. Today, approximately 16% of top pharmaceutical drugs--and 35% of [...]
Properties Affecting Homogeneity in Semi Solid Manufacturing
Semi solids such as creams, lotions, gels, and ointments require homogeneity in order to work properly, and maintaining proper homogeneity begins in the semi solid manufacturing process. Though semi solid products may not command the [...]
Reducing Contamination in Parenteral Manufacturing
Emphasizing quality and compliance through every step of the manufacturing process helps to ensure the safety and consistency of parenteral products. Manufacturing parenteral products--from prefilled syringes and single-use vials to premixed IV bags and beyond--offers [...]
Manufacturing of Capsules Requires Formulation Adaptations
APIs, excipients, capsule materials and production methods should all complement one another in order to prevent difficulties. Whether a drug formulation exists as a liquid, granule or gel, capsules can serve as a useful oral [...]