Regulatory Guidelines for Natural Products
Regulatory guidelines for natural products ensure the safety, efficacy, and quality of herbal medicines, dietary supplements, and other natural-based therapeutics. Authorities like the FDA, EMA, and WHO establish standards for manufacturing, labeling, and marketing to protect consumer health. These guidelines include requirements for Good Manufacturing Practices (GMP), proper clinical testing, and quality control measures, ensuring that natural products meet established pharmacopoeia standards. Additionally, regulations address issues of adulteration, contamination, and standardization of active ingredients. With the increasing global demand for natural products, robust regulatory frameworks are essential to guarantee product integrity, support consumer trust, and promote sustainable use of natural resources.
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Regulatory Guidelines for Natural Products Conference Speakers
Recommended Sessions
- Aquatic Ecosystems and Medicinal Properties
- Bioactive Compounds: Discovery and Characterization
- Biotechnology in Medicinal Plant Research
- Drug Development from Marine Resources
- Ethno pharmacology: Indigenous Healing Practices
- Ethnobotany: Traditional Knowledge and Modern Applications
- Herbal Medicine in Integrative Healthcare
- Marine Toxins and Therapeutic Potential
- Marine-Derived Pharmaceuticals: Innovations and Trends
- Microbial Symbionts in Medicinal Plants
- Natural Products in Cancer Therapeutics
- Novel Formulations and Drug Delivery Systems
- Nutraceuticals and Functional Foods
- Pharmacognosy: Quality Control and Standardization
- Pharmacology of Medicinal Plants
- Pharmacovigilance and Safety Assessment
- Phytochemistry and Analytical Techniques
- Plant-Microbe Interactions in Drug Synthesis
- Regulatory Guidelines for Natural Products
- Sustainable Harvesting and Conservation Strategies
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