CD Formulation Documents
Accelerated Shelf-Life Testing
Active Pharmaceutical Ingredient Excipients
Adsorbents, Desiccants and Humectants
Amino Acid Series Active Pharmaceutical Ingredients
Amorphous Solutions and Dispersions
Antibacterial, Anti-inflammatory and Antiviral Series Active Pharmaceutical Ingredients
API Chemical Modification
API-Excipient Compatibility
Bacterial Endotoxin Testing
Bacterial Endotoxin Testing
Cardiovascular Series Active Pharmaceutical Ingredients
Chromatographic Analysis of Pharmaceutical Preparations
Coated Tablets
Compaction Excipients
Controlled Release Excipients
Co-processed Excipients
Cosmetic Ingredients
Cosmetic Preservatives
Cosmetic Sweeteners
Detection of Fluorescent Whitening Agents in Pharmaceutical Packaging Materials
Determination of Contact Angle of Pharmaceutical Excipients
Determination of Water Vapor Transmission Capacity of Pharmaceutical Packaging Materials
Disinfection Efficacy Testing
Drug Delivery System Development
Drug Formulation and Packaging Compatibility
Dry Powder Inhalation Excipients
Elemental Impurities Analysis
Embryonic Microspheres Preparation
Enteral Nutrition Formulation Development Solutions
Flavoring Chemical Agents
Food Preservatives
Fragrance Agents
Headspace Gas Analysis for Pharmaceutical Packaging
Hollow Microneedle Technology
Hormone Series Active Pharmaceutical Ingredients
Hot Melt Extrusion Excipients
Hot Melt Extrusion Technology for Microspheres Preparation
Hydrotropy Agent Excipients
Influencing Factors Analysis
Leavening Agents
Long-Term Accelerated Shelf-Life Testing
Loss-on-Drying Test
Microencapsulation Technology
Microsphere and Microneedle Patch Preparation Services
Multiparticulate System Formulation Development
Multiparticulate System Formulation Development
Multiparticulate System Formulation Development
Nanomilling to Prepare Small Particle Size Drug Particles
Nanoparticle Development Services for Drug Delivery System
Non-Volatile Residue (NVR) Test
Oral Thin Films Technology Services
Osmotic Pressure Regulators
OTR & WVTR Test
Particulate Matter Test
Penetration Enhancer Excipients
Polymeric Microspheres Preparation
Powder Health Products Development
Preformulation
Preparation of Polymer Micellar Drug Carrier
Prescription Screening Process Analysis
Propellant Cosmetic Chemicals
Readily Carbonizable Substances Test
Residual Oxygen & Dissolved Oxygen Test
Residue On Ignition Test
Sealing Test of Pharmaceutical Packaging Materials
Self-emulsifying Drug Delivery System
Solids Dosage Forms Development
Solubility Analysis
Stability Analysis
Stabilizers and Thickeners
Sterility Test
Stiffening Agents
Surfactant Excipients
Thermal Shrinkage Test of Pharmaceutical Packaging Materials
Transdermal Patches Drug Delivery System
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The purpose of CD Formulation's headspace analysis tests for pharmaceutical packaging is to detect the residual gas content in pharmaceutical packaging and to adjust the packaging process accordingly. The residual gases inside the package should not be disregarded at the end of the packaging process. It is very difficult to control and change the gas content inside the package from the end of filling until the product is opened and used. The use of barrier packaging materials can only prevent the gas from entering/leaking out of the packaging material, but cannot eliminate the oxygen and other gases already inside the package (excluding the case of adding deaeration technology to the package). If the content of residual gas exceeds the maximum concentration required for product preservation, no matter how good the high barrier material and how well sealed packaging form can not meet the shelf-life requirements of the product. Therefore, it is necessary to detect the residual gas content in the package and adjust the packaging process accordingly. Learn more at https://www.formulationbio.com/headspace-gas-analysis-for-pharmaceutical-packaging.html.