Pharmaceutical Manufacturing Facility Licensing in the UAE (EDE)
Companies setting up a pharmaceutical manufacturing facility in the UAE don’t just secure a commercial license and start production. They
Pharmaceutical Drug Patent Expiry: Price Impact, Regulatory Challenges & More
A pharma product’s lifecycle will reach a significant milestone in the form of patent expiry. In an initial drug development
Pharmaceutical Excipients Definition, Types & Regulatory Guidelines
A drug product gets its therapeutic effects from the active pharmaceutical ingredient (API). However, finished pharmaceutical products also have ingredients
Food Packaging and Labelling Requirements in the UK
On September 4, 2026, the UK Food and Standards Agency released packaging and labelling guidance. It provides the legal requirements
Cosmetic Safety Assessment & Global Regulatory Standards
The world of cosmetics is growing rapidly. While diverse cosmetic products are being released, it is important not to compromise
Pharmaceutical Artwork Management: Challenges, Solutions, AMS, Benefits
Pharmaceutical labels don’t change with just a few word edits on the file. One regulatory update triggers a chain of
Health Supplements Regulations & Voluntary Notification in Singapore
Selling a health supplement in Singapore doesn’t involve a registration certificate or a licence. There’s no approval letter to wait
Modernization of Cosmetics Regulation Act of 2022 (MoCRA): US FDA Requirements
The Modernization of Cosmetics Regulation Act of 2022 (MoCRA) was enacted on December 29, 2022. It came as part of
CDSCO Regulations for New Cosmetics in India
New cosmetics in India are those with novel ingredients that haven’t been used anywhere in the world before and aren’t