Bill of Materials (BOM) Number in Pharmaceuticals
#121 Production
Bill of Materials (BOM) Number in Pharmaceuticals

A BOM (Bill of Materials) number serves as a unique identifier for a specific set of materials associated with a Master...

PIC/S Classification System for Pharmaceutical Sterile Products
#122 Production
PIC/S Classification System for Pharmaceutical Sterile Products

The Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme (PIC/S) is an international...

Clinical Toxicology - Short Note
#123 Toxicology
Clinical Toxicology - Short Note

Clinical toxicology deals with the assessment and treatment of persons exposed acutely or chronically to potentially...

Raw Material Test Method - Zinc Sulfate Monohydrate
#124 STP
Raw Material Test Method - Zinc Sulfate Monohydrate

Freely soluble in water: Take about 0.1 g of test sample into a clean and dry test tube. Add 1 ml purified water and...

Purified Water Test Procedure in Pharmaceuticals
#125 Quality Control
Purified Water Test Procedure in Pharmaceuticals

i) Appearance: Clear, odorless and colorless liquid. ii) pH: Transfer 100ml water to a suitable container; add 0.3ml...

Liquid Dosage Forms in Pharmaceutics: Advantages and Classification
#126 Technology
Liquid Dosage Forms in Pharmaceutics: Advantages and Classification

Pharmaceutical Liquid dosage forms represent a diverse category of pharmaceutical preparations that include solutions,...

Short Notes on HPLC Peak-to-Valley Ratio
#127 Analysis
Short Notes on HPLC Peak-to-Valley Ratio

The Peak-to-Valley ratio (P/V ratio) is a critical chromatographic system suitability parameter used to evaluate how...

HPLC Method Development in Pharmaceuticals
#128 R&D
HPLC Method Development in Pharmaceuticals

Analytical method development is a critical process in pharmaceuticals. The variety of columns, operating parameters,...

Pharmaceuticals Manufacturing Process (Tablet Compression)
#129 Production
Pharmaceuticals Manufacturing Process (Tablet Compression)

A Quality by Design (QbD) approach to understanding tablet compression failures and preventing them through proper...

70% IPA is the Ideal Disinfectant in Pharmaceuticals
#130 Production
70% IPA is the Ideal Disinfectant in Pharmaceuticals