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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Determination of Water Vapor Transmission Capacity of Pharmaceutical Packaging Materials: Water vapor transmission capacity refers to the amount of water vapor through the specimen in a certain period of time under the specified temperature, relative humidity, and certain water vapor pressure. The main role of the drug bottle is to protect the safety of drugs in the process of storage and transportation, to ensure the stability of the validity period. Water vapor transmission amount can reflect the barrier performance of the bottle, if this indicator exceeds the standard, it is easy to cause moisture in the long storage of drugs, affecting the safety of medication. Whether the water vapor transmission capacity of the bottle meets the standard is related to the purity of the raw materials used, the control of the production process, the quality of the mold and other factors, high-quality packaging is the key to protect the safety of drugs, but also an effective way to improve the added value of the product.