Pronunciation: [dˈɑːɹuː] (IPA) 
The word "DARU" is commonly spelled with four letters, but it can also be written as "DORU" depending on the region where it is used. The IPA phonetic transcription for "DARU" is /ˈdɑːru/, while for "DORU" it is /ˈdɔːru/. The difference lies in the vowel sound, with "DARU" using the long "a" sound and "DORU" using the long "o" sound. These two spellings are both correct and can be used interchangeably in different contexts.
DARU stands for Drug Administration and Registration Unit. This term is mainly used in the context of pharmaceutical and drug regulation in certain regions, such as India and Bangladesh.
The Drug Administration and Registration Unit, commonly known as DARU, refers to a regulatory body responsible for the administration and registration of drugs in a specific jurisdiction. It is an official authority that ensures the safety, efficacy, and quality of pharmaceutical products available in the market.
DARU serves as a crucial intermediary between drug manufacturers and healthcare consumers. It establishes guidelines, regulations, and protocols that pharmaceutical companies must adhere to when developing, manufacturing, and distributing drugs. The primary objective of a DARU is to protect public health by ensuring that the drugs available on the market are safe for use, effective in treating the intended conditions, and of high quality.
The responsibilities of a DARU typically include reviewing and approving applications for drug registration, conducting inspections to assess compliance with regulatory standards, monitoring adverse reactions and drug safety data, and taking appropriate actions to address any non-compliance or safety issues. DARU may collaborate with other regulatory bodies, such as the Food and Drug Administration (FDA), to ensure harmonization of regulations and facilitate international trade of pharmaceutical products.
Overall, DARU plays a crucial role in safeguarding public health by regulating the production, distribution, and use of drugs, ensuring that they meet the required standards and do not pose any harm to individuals.
