What does DRAP mean in DRUGS


The Drug Regulatory Authority of Pakistan (DRAP) is responsible for regulating and monitoring the manufacturing, distribution, prescription, retailing and importation of drugs in Pakistan. It works to ensure that all pharmacists, practitioners, and healthcare institutions are following drug-related laws and regulations. DRAP's mission is to ensure safe use of medicines by providing safety regulation, quality assurance and rapid access to essential medicinal products in the country.

DRAP

DRAP meaning in Drugs in Medical

DRAP mostly used in an acronym Drugs in Category Medical that means Drug Regulatory Authority of Pakistan

Shorthand: DRAP,
Full Form: Drug Regulatory Authority of Pakistan

For more information of "Drug Regulatory Authority of Pakistan", see the section below.

» Medical » Drugs

Essential Questions and Answers on Drug Regulatory Authority of Pakistan in "MEDICAL»DRUGS"

What is the role of DRAP?

The Drug Regulatory Authority of Pakistan (DRAP) is responsible for regulating and monitoring the manufacturing, distribution, prescription, retailing and importation of drugs in Pakistan. DRAP seeks to ensure that all pharmacists, practitioners, and healthcare institutions are following drug-related laws and regulations.

How does DRAP work to promote safety?

DRAP works to promote safety through regulation and quality assurance. It creates regulations on drug production processes, monitors drug manufacture for consistency with good practice principles such as GMP standards or other WHO guidelines. Additionally it regulates the selling of drugs either through pharmacies or online outlets.

Who oversees DRAP?

The Ministry of National Health Services Regulations & Coordination (NHSRC) is the Government agency responsible for overseeing Drug Regulatory Authority in Pakistan (DRAP).

How can I access information about drug regulatory affairs?

All information on regulatory affairs related to pharmaceuticals can be found on DRAP's website at https://www.drap.gov.pk/. Information may include license registration requirements, product reviews and inspections, advertising restrictions etc.

Are there any fee exemptions available?

Yes. The Drug Regulatory Authority has put exemptions in place for certain categories including health professionals working with the public sector under Agreement/Contract between Federal or Provincial Government ministry or department with a government medical institution; or charitable organizations registered with government authority; or individuals who provide services free of charge or at nominal charges.[END]

Conclusion: The Drug Regulatory Authority of Pakistan (DRAP) is an important agency charged with monitoring and regulating pharmaceutical products across Pakistan. Its main objectives are ensuring that all pharmacists, practitioners, healthcare institutions are following proper drug-laws and regulations as well as promoting safety through regulation and quality assurance initiatives for drugs produced in the nation. These efforts help ensure that everyone has access to safe medicines throughout the country.

Final Words:
The Drug Regulatory Authority of Pakistan (DRAP) is an important agency charged with monitoring and regulating pharmaceutical products across Pakistan. Its main objectives are ensuring that all pharmacists, practitioners, healthcare institutions are following proper drug-laws and regulations as well as promoting safety through regulation and quality assurance initiatives for drugs produced in the nation. These efforts help ensure that everyone has access to safe medicines throughout the country.

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