EDE Product Classification in the UAE: Process, Requirements & Fees
Companies need to determine the regulatory classification and applicable requirements for a product before bringing it into the UAE market.
Cosmetic Manufacturing Licence in India: CDSCO Rules & Process
Cosmetics manufactured in India are regulated under the Drugs and Cosmetics Act, 1940, and the Cosmetics Rules, 2020, for sale
What Are IQ, OQ & PQ in Pharmaceuticals?
Every piece of equipment used in pharma manufacturing has a direct impact on product quality. If a machine fails, the
Computer System Validation (CSV) In Pharma
Computer systems are widely used in the pharmaceutical industry. That’s why computer system validation (CSV) and other risk-based assurance approaches
Investigational New Drug (IND) Application Process, Types and Requirements
Federal law requires drugs to have an approved marketing application before transportation or distribution across state lines. However, a drug
Pharmaceutical Packaging Graphic Design Challenges and Solutions
Pharmaceutical packaging is more than a visual representation of medicine. The packaging and its artwork must communicate critical product information
Drug Regulations in India and CDSCO Approval Process
Working with the Central Drugs Standard Control Organisation (CDSCO) is part of almost every drug-related regulatory pathway in India. The
Phytopharmaceutical Regulations in India: CDSCO Approval Process & Requirements
Phytopharmaceuticals are basically plant-based drugs, but they are developed in a more scientific way than the usual herbal products we
Drugs & Pharmaceutical Products Regulations & Registration in Thailand
Every finished pharmaceutical product for human or animal use in Thailand needs drug registration with the Thai FDA. Only then