On-Demand Webinars
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OSD Manufacturing For Pediatrics And Other Special Patient Populations
8/29/2024
Watch to hear Steven Facer, Adare's Vice President of Business Development EU/ROW, discuss the challenges of pediatric oral solid dose manufacturing and how to overcome them.
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From Powder To Particles With Jet Milling
Gain valuable insights into the jet milling process and Quality by Design approach for inhalation drug delivery and their potential applications in drug development.
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Rapid Development Of Amorphous Solid Dispersions For Bioavailability
See how an amorphous solid dispersion (ASD) of acalabrutinib was designed using in vitro studies and in silico modeling. Understand how ASD formulations can enhance bioavailability.
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Regulatory, Cost Implications Of Switching Injectable Delivery Formats
Launching a large molecule in one format and then switching the delivery format often transpires as a lifecycle management strategy for cost efficiency, supply chain continuity, and patient benefit.
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Managing Risks In Injectable Drug Delivery
3/13/2025
Gain insights pertinent to efficient and effective drug development. Understand and execute a risked-based critical thinking approach related to injectable drug packaging and delivery.
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Challenges Associated With In-Use Simulated Administration Of Biologics
Explore some of the more challenging aspects surrounding in-use testing for parenteral delivery along with potential strategies to address these issues.
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Solid Form Screening Of Active Pharmaceutical Ingredients
Explore the role of solid form services in helping meet accelerated timelines of the drug development lifecycle along with examples of robust workflows for fast and thorough solid form screens.
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Taste Masking 101: Sensory And Performance Evaluation
7/11/2022
Learn how techniques and innovations in taste masking sensory and performance evaluation can help accelerate your formulation development and confirm desired taste profile.
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How To Bring Your LNP Formulation To Clinical/Commercial Manufacturing
Gain valuable insights into key considerations when selecting lipid excipients for LNP formulations and the process development steps necessary to advance them to GMP manufacturing and clinical trials.
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Accelerating Nasal Dosage Form Development From Early-Phase To Clinical Trial Manufacture
10/21/2024
Led by Dr. Richard Johnson, Chief Scientific Officer, this 40-minute session covers the five key stages of the UpperNose development platform, highlighting the significance of target product selection and its influence on formulation and clinical outcomes.