Barrett Rabinow
Ph.D. ·
skokie, IllinoisOrganic Chemistry
Pharmaceutics
Pharmaceutical R&D
Sterile Manufacturing
Root Cause & CAPA Issues
Process Improvement
R&D Acquisition Analysis
Program Plan Development
New Product/Process Design
Patent Analysis
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Technical Feasibility Analysis
Drug Delivery Platforms
Nanosuspension Drug Formulation
IV Solutions
Good Distribution Practices
Leachables and Elemental Impurities Testing
Manufacturing Process Troubleshooting
Corrosion Issues
Chemical Problem Solving
FDA Negotiations
pH and Particulate Issues
Storage Labeling
Anti-adhesion Therapeutics
Contaminant Identification
IV Container Extractables
Analytical Chemistry
Drug Reformulation
Amino Acid Analysis
Aluminum Methodology
Large Volume Parenteral Solutions
Osmolarity
Stability Storage Labeling
Medical Device Leachables Evaluation
Physical-Organic Chemistry
Clinical Chemistry
Electrochemistry
Propofol Formulation
Submicron Particles of Antineoplastic Agents
Drug Delivery Compositions and Methods
Antimicrobial Drug Resistance Treatment
High-Pressure Sterilization
Heart Rate Control
Drug Delivery to the Brain
Injectable Dosage Forms
Biopharmaceutical Development
Parenteral Pharmaceuticals
Intra-Articular Drug Delivery
Heparin Analysis
Itraconazole Formulation
Excipient Selection for Injectable Dosage Forms
Plastic Packaging Materials
Hydrophilic Surfaces
Protein Adsorption
Cisplatin Degradation
Parenteral Products Analysis
Water Vapor Transmission Rate
Dialysis Solutions
Trace Metal Contaminants
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