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…
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…
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…
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…
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…
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…
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…
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…
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…