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THINKING
Science
Matrix Approach to Media Fills
Expediting a Promising New Therapy with RP Scherer Softgel Technology
Adulterants in NMR Spectroscopy
Antibodies to a Derivatized Protein
Detecting Residual Solvents in API
Extractable Silicone Oil
Fast-Into-Man Model for DPI
Filling Dry Powder Inhalers (DPIs)
Immunogenicity Uses Affibody
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Ligand
The Importance of ODTs
Injectable Development
Kollicoat Protect Top-Coat
A Measured Dose
Moisture Validation for PMDIs
Nanoparticulate Zydis
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Fast Dissolve
Optiform™ Technology
Overcome Assay Drift in PK ELISA
Phosal
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MCT Softgel
Plasticizers Affect Softgel Stability
Rapid-Screening Nebulizer Formulation
Separate Derivatized Protein in Serum
Vegicaps
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Capsule Innovation for High Viscosity Material
Standardize GMP Potency Validation
Cells: Practical Considerations For Bioassays
Overcoming Challenges in Technical Transfer
Development/NDA-Level Validation of a Real-Time PCR Procedure
Selecting the Right Technology for Poorly Soluble Compounds
Virus Safety of Biopharmaceuticals
NMR Spectroscopy in the Characterization of Specialty Polymers
The Impact of a Poorly-Soluble Drug On Disintegration of ODT's
Pharamcokinetics of Fenofibrate Nanoparticles Stabilized
Gelatin-Free Capsules: Investigation Into Properties
Evaluation of Digestion Approaches for Determination
Development of Digestion Methods for Determination
Development and Validation of A Method for Determination
Completing The Impurity Picture
Stability Studies in Pharmaceutical Development
Patient Compliance Study
Characterization of Trace Impurities
Zydis
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Fast-Dissolve Case Study
Experience in Ensuring Viral Safety
SEDDS/SMEDDS Compatibility with Vegicaps
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Capsules
Softgel Technology as a Tool for Bioavailability Enhancement
Advances in Aseptic B/F/S Processing of Pharmaceutical Liquids
Formulation Considerations for Inhaled Products
Defining and Addressing Solid-State Risks
Peptides in Anti-Aging Functional Cosmetology
Virus Safety of Biopharmaceuticals
Issues in Assuring Virological Safety of Biopharmaceuticals
Comparison of GPEx
®
to Traditional Cell Line Engineering
Recent Advances in Tablet Applications
Dosage Forms for Oral Delivery of Liquid Lipid-Based Formulations
Development of Lipid-Based Drug Delivery Systems
LBDDS for Oral Delivery of Macromolecules
Market Insights
Accelerate Bioassay Transfer in GMP
Consumers Prefer Oral Dosage Forms
Meet a Catalent Drug Delivery Exec
Outsource Inhalation Development
Recent FDA guidance on ODTs
Strategic Outsourcing
Trends: Drug Development
Why Outsource Stability Programs?
Catalent Exec Discusses Blow/Fill/Seal
Building Prefilled Syringe Capacity for the Future
Cutting The Fat
Prefilled Syringes Pinpoint Stability, Compatibility & Safety
Drug Delivery Roundtable
Patient Adherence Presentation
Advanced Drug Development and Delivery Solutions
Patient-Administered Therapies Drive New Delivery System Designs
Designing In Adherence
Solubility Roundtable
Ensure Compliance Excellence
Challenges Working With International Suppliers
Discussion On Emerging Drug-Delivery Technologies
Leveraging Market Intelligence
Reigniting Innovation
Prefilled Syringes: Designed,Sealed and Delivered
Catalent Eyes Emerging Market Expansion
Case Studies in Pharmaceutical Project Management
Aseptic Processing Utilizing the Blow/Fill/Seal Process
Catalent Plans Single Use Overhaul of Bioreactors
Solutions For Controlled Release Technologies
Catching up on Development & Clinical Services
Pharma Outsourcing
Evolving Industry Needs Require Evolving Partners
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Better Technical Transfer for Steriles
Catalent’s Lean System
Track-and-Trace Technology
Changes Affect Clinical Trials
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Cold Chain: A Case Study
A Comprehensive Approach to Patient Adherence
Solving Tech Transfer Challenges for Complex Products
Right Place, Right Time
Webinars
Strategies for Effective Clinical Supplies Management
Accelerate the Development of Challenging Drug Candidates via Crystal Engineering
Biosimilars: Creating Workable Solutions to Global Regulatory and Analytical Challenges
Omega-3 Innovations in Pharmaceutical and Diagnostic Markets
Bioavailability Enhancement Using LBDDS
Hot Melt Extrusion and OptiDose™ Technology
Solid-form Discovery and Development Webinar
Considerations For An Immunogenicity Program Webinar
Leachables and Extractables: Regulatory Context Webinar
Clinical Packaging: Driving Efficiencies
Stability Studies in Pharmaceutical Development Webinar
BCS Type II & IV Compounds Webinar
Global Clinical Supply Chain Management Webinar
Generation of Mammalian Cell Lines Webinar
Vitamin D3 Analogs Delivery Systems Webinar
NEWS & EVENTS
News
Catalent Breaks Ground of its Winchester, KY CR Manufacturing Facility
Catalent Announces Opening of New Single-Use Biomanufacturing Center
Worldwide Competition Recognizes Next-Generation Scientific Talent
Catalent Experts Exhibit and Present at BIO and Interphex 2013
Catalent Wins Two Prestigious Process Excellence Awards
Events
PDA Annual Meeting
World Drug Delivery & Formulation
Clinical Trial Supply Europe
Cell Culture World Congress
Bio Europe
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