The General Purpose Financial Report presents an overall picture of the financial performance of the Central Public Sector Enterprises (CPSEs) which are under the audit jurisdiction of the Comptroller and Auditor General of India (CAG).
CAG is an independent authority under the Constitution of India. He is the head of the Indian audit & account department and chief Guardian of Public purse. Shri Rajiv Mehrishi is the incumbent CAG of India.
The Comptroller and Auditor General (CAG) is a constitutional functionary, independent of Parliament/legislature and executives. The CAG is responsible for. Audit of Ministries and departments of Government of India and the State Governments.
UPSC May also ask you the difference between CGA and CAG. While CAG is a constitutional body, CGA is not. While CAG is independent constitutional body, CGA works under Ministry of Finance and not a constitutional or statutory body.
NEW DELHI: All you need to get India's top drug job — Drug Controller General of India (DGCI) — is a simple graduation in pharmacy or a graduate degree in medicine with post-graduation in clinical pharmacology or microbiology (MD) along with five years' experience.
When a company in India wants to manufacture/ import a new drug it has to apply to seek permission from the licensing authority (DCGI) by filing in Form 44 also submitting the data as given in Schedule Y of Drugs and Cosmetics Act 1940 and Rules 1945.
The Directorate General of Commercial Intelligence & Statistics (DGCIS) is the premier organization of Government of India for collection, compilation and dissemination of India's trade statistics and commercial information. The EDI data is transmitted on-line daily through Indian Customs EDI Gateway (ICEGATE).
Eswara Reddy was appointed the Drugs Controller General (India) in February 2018. He is the youngest Drugs Controller General (I) who has worked for all the positions of the hierarchies. He promoted as Assistant Drugs Controller of India in 2009 and appointed as Deputy Drugs Controller (India) in 2012.
Triage refers to the process of placing a potential adverse event report into one of three categories: 1) non-serious case; 2) serious case; or 3) no case (minimum criteria for an AE case are not fulfilled).
CDSCO Overview - India Central Drugs Standard Control Organization. The Central Drugs Standard Control Organization is the Indian regulatory body for pharmaceuticals and medical devices, being the equivalent of the FDA in the US.
Established in November 2008, the India Office serves as the lead FDA on-site presence in India. The mission of the New Delhi-based office is to help ensure the safety, quality, and effectiveness of medical products and food produced in India for export to the United States.
An online licensing portal of Central Drugs Standard Control Organization (CDSCO) has been implemented on January 2016 and has been named “SUGAM†to file applications for various services like Application Submission, Processing and Grant of permission for quick delivery of services.
