Capsule Production White Papers & Case Studies
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5 Steps To Increase Energy-Efficient Mixing
3/1/2018
Mixer testing simulation trials are necessary to confirm the suitability of a specific mixing strategy. Explore five ways to increase energy efficiency in new and existing mixing processes.
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Efficiencies In Powder Dispersion For Manufacturers
3/1/2018
Uniformly dispersing powders into a liquid batch in a practical amount of time is a common problem for F&B manufacturers. This white paper explores five tips for dispersing powders more efficiently.
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Development Of Biopharmaceuticals Requiring Lyophilized Formulations
1/18/2018
Development of a drug formulation and lyophilization (freeze drying) process begins with laboratory experiments followed by scale up to larger lyophilizers.
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Modular Facility Design: A Cost-Effective Option In The Post-Blockbuster Drug Era
9/1/2015
The pharmaceutical industry has undergone a sea of change in recent years as manufacturers have adapted to the end of the era of large-volume production of mass-market blockbuster drugs. With firms now focusing in on subpopulations of patients, there is a need for lean, adaptable facilities that can switch quickly between multiple products in multiple formats. Modular facilities can meet this need. While not a panacea, for the right project characteristics, ‘Modularity in Design’ can deliver significant and quantifiable long-term value.
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Medication Errors -- A Threat To Patient Safety: Mitigating Errors With Tablet Appearance
1/16/2014
Medical prescription drug errors by doctors, pharmacists and patients account for 1.5 million incidences of sickness, injuries or deaths in the U.S. each year. By Jay Anbil and Steve Yoder
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Film Coating For Pediatric Oral Solid Dosage Forms
1/16/2014
From a recent survey conducted within the pharmaceutical industry, by Colorcon, it was confirmed that oral solid dosage forms are a preferred choice for formulation of pediatric medicines.
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Accelerating Lipid-Based Drug Formulation
7/23/2013
Formulation scientistsmust develop and validat robust systems that address the challenges posed by increasingly complex drug candidates, in ever shortening time frames.
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When Capsules Fall Apart, Who Is To Blame?
5/6/2013
Capsule integrity is a given for established manufacturers with impeccable reputations. Consumers, however, know from experience that not all capsules are made equal. Some can be difficult to extract from the blister pack. Others may have gel caps with cracks or, even worse, ruptures that allow the ingredients to spill out. Is this a manufacturing problem? Or has R&D neglected to implement a fool proof test methodology for evaluating capsule stability? Compression and tension testing offer a technical approach with quantifiable results that can be used to assess capsule performance.
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Hypromellose Capsule For Optimum Formulation Of Pharma Dosage Forms
Hypromellose capsules were originally formulated with a secondary gelling agent. This article discusses the rationale for developing Capsugel’s Vcaps Plus capsules without a gelling agent.
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Ribbon Blenders: A Best Practices Guide
This white paper presents some basic best practices for efficient processing in a Ribbon Blender. The ideas discussed here are recommendations based on practical and technical experience gained by Ross over several decades as a leading supplier of Ribbon Blenders to the process industries worldwide.