Cell and Gene Therapy Products: Meaning, Types & Global Regulations
Cell and gene therapy (CGT) products are advanced biological treatments. They can change cellular functions or genetic materials to potentially
Pharma Regulatory Contract Staffing: Benefits, Roles & Use Cases
The pharmaceutical industry is highly regulated. Companies need to comply with it to launch their new drugs in the market.
Precision Medicine in 2026: Key Players, Technologies, and Drug Pipeline
Precision medicine involves the same diagnosis for multiple patients but completely different treatments for each of them. There’s no “average”
Food Supplements Regulations & Notification Process in Belgium
Before marketing, food supplements must comply with the applicable Belgian and EU food legislation and notification requirements. These cover their
Pharmaceutical Regulations in China: NMPA Drug Registration Guide 2026
NMPA is the regulatory body that manages the launch of pharmaceutical products in China. It authorizes your product after drug
Dietary Supplements Regulations & Registration Process in Egypt
Before importing or marketing dietary supplements in Egypt, companies need to determine the applicable regulatory route based on the product
Dietary Supplement Regulations & Registration Process in Colombia
In Colombia, INVIMA issued 2025 alerts about dietary supplements that were being sold through websites and other channels. They didn’t
Food Supplement Regulations & Notification Process in the Czech Republic
To place food supplements on the Czech market, the food business operator must ensure compliance with two sets of regulations:
Health or Dietary Supplements Regulations & Registration Process in Bangladesh
Bangladesh regulates health supplement/dietary supplement products under its food-safety framework through the Food Safety (Health Supplement/Dietary Supplement, Food for Special