- Benefits of Submitting Master Formulation Records
- CBD Testing
- Challenges Facing an Analytical Laboratory
- Chemical Testing Aspects of USP 797 for Compounded Sterile Preparations
- Compounding Slow-Release Pharmaceuticals
- Container Closure Systems
- Data Integrity
- Drug Diversion
- Drug Formulation and Its Impact on Analytical Testing
- Evaluation of Topical Dispenser Systems for Vaginal Delivery of Feminine Medications
- Expiration Dates and Retesting of API
- Extending Beyond Use Dating for Compounded Preparations
- Gas Chromatography
- Glossary of Quality Control Quality Assurance Terms in Pharmaceutical Compounding
- High-Performance Liquid Chromatography
- Importance of Forced Degradation in Stability Indicating Methods
- Importance of Sample Amounts and the Impact on Potency Testing
- Importance of Testing Bulk Substances
- Importance of Testing Raw Material Components
- Ophthalmic Medication and Particulate Matter
- Particulate Matter – What is It and What are the Concerns?
- Particulate Matter in Injections What is It and What are the Concerns
- Particulate Matter Testing
- Potency Test Failure Case Studies
- Potency Testing Benefits and Requirements
- Quality Control or Quality Assurance
- Quality-Control Analytical Methods - Homogeneity of Dosing Forms
- Stability vs. Potency Testing
- Topical Metered-dosing Dispenser Performance Evaluation
- U.S. Food and Drug Administration Inspection--Releasing a Sample to the U.S. Food and Drug Administration
- USP <800> Why should you test
- USP Surface Wipe Sampling
- Validated Potency Methods – NonGMP
- What Factors Influence Stability?
- Applications and Sterility of Autologous Serum Eye Drops
- Basics of Sterility Testing
- Comparison of Endotoxin Testing Methods for Pharmaceutical Products
- Discussion of USP Chapter 71, Sterility Tests
- Dry Heat Sterilization of Parenteral Oil Vehicles
- Endotoxins
- Endotoxin Essentials
- Endotoxin Limits
- Essentials of USP <51>
- Essentials of United States Pharmacopeia Chapter 51 Antimicrobial Effectiveness Testing
- Growth Media Differences
- Growth Promotion Testing
- How Does Microbial ID Benefit Your Pharmacy?
- Importance of Endotoxin Testing
- Laboratory Considerations of USP Chapter 71 Sterile Tests
- Media Fill Testing
- Method Suitability and Its Importance to the Test Method
- Microbial Disinfectant Cleaning Challenge Studies
- Microbial Identification
- Microbial Limit Tests for Nonsterile Pharmaceuticals Part 1
- Microbial Limit Tests for Nonsterile Pharmaceuticals-Part 2
- Microbial Tests for Non-Sterile Products
- Microbial Testing Aspects of USP 797 for Compounded Sterile Preparations
- Open vs Closed Membrane Filtration Systems
- Prevent Future Sterility Failures by Identifying Contaminating Microorganisms
- Quality of Sterility Testing
- Rapid Sterility Testing
- Rapid Sterility Testing for Compounding Pharmacies
- Sterility Test Failure: Possible Causes and Investigation
- USP <51> Antimicrobial Effectiveness Testing
- USP <61> and USP <62> Microbial Tests for Non-Sterile Products
- USP <71> Sterility Testing
- USP <85> Bacterial Endotoxin Validation and Its Importance to the Test Method
- Chemical Stability of Admixtures Containing Ziconotide 25 mcg-mL and Morphine Sulfate 10 mg-mL or 20 mg-mL During Simulated Intrathecal Administration
- Compatibility and Stability of Palonosetron Hydrochloride and Propofol During Simulated Y-Site Administration
- Compatibility and Stability of Palonosetron Hydrochloride with Four Neuromuscular Blocking Agents During Simulated Y-Site Administration
- Compatibility and Stability of Palonosetron Hydrochloride with Gentamicin Metronidazole or Vancomycin During Simulated Y-Site Administration
- Compatibility of Caspofungin Acetate Injection with Other Drugs During Simulated Y-Site Coadministration
- Compatibility of Micafungin Injection with Other Drugs During Simulated YSite Coadministration
- Drug Compatibility with a New Generation of VISIV Polyolefin Infustion Solution Containers
- Palonosetron Hydrochloride Compatibility and Stability with Three Beta-Lactam Antibiotics During Simulated Y-Site Administration
- Physical and Chemical Stability of Palonosetron Hydrochloride with Glycopyrrolate and Neostigmine During Simulated Y-Site Administration
- Physical and Chemical Stability of Palonosetron with Metoclopramide and Promethazine During Simulated Y-Site Administration
- Quality Control Analytical Methods-Stability Versus Potency Testing-The Madness is in the Method
- Stability of Metronidazole Benzoate in SyrSpend SF One-Step Suspension System