Optimal Oral Drug Delivery for Pediatrics
Addressing the Unique Challenge of Pediatric Medication Dosage Delivery in the Pharmaceutical Industry. Establishing suitable dosage regimens for pediatric patients is an…
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How to Accelerate Your Drug Product Development
DRUG DEVELOPMENT AND FORMULATION IS SCIENCE. DOSE DESIGN TO CREATE SUCCESSFUL TREATMENTS IS ART. Developing successful treatments that meet the needs of…
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Mapping the Pathway to Designing Successful Treatments
Efficient, comprehensive transitions from early phase (preclinical up to phase 1) to late phase (phase 2 and beyond) are critical to the…
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The Role of Roller Compaction in Dose Design
Introduction: Roller compaction is a popular dry granulation process with some significant advantages over wet granulation processes. It offers better overall stability…
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Commonly Asked Questions about Elemental Impurities
If scientific literature indicates that elements are not likely to be present in drug product components, and no additional elements are added…
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Precision Formulation via Small Batch Optimization
It is typical to encounter a restricted number of APIs during the initial stages of drug development. This limitation hinders the swift…
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Raman Spectroscopy in Product Formulation Analysis: A Deep Dive.
Comparing the dissolution rates and pellet fine structure of branded Zovirax® with three similar acyclovir generic products marketed across the world, all…
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Customer Requirements for Oral Dose Development
Pharmaceutical developers aim for cost-effective oral medications that work well. This can be challenging, requiring an understanding of client, patient, and provider…
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Translating Lab Discoveries: Preclinical to First-in-Human Development.
Overview Drug developers have to take into account several factors to position a pre-clinical drug candidate successfully for first-in-human clinical trials. This executive summary will outline…
