Mcq on cdsco
Web12 aug. 2024 · Solved Question Paper of Recruitment Test (Computer Based Recruitment Test) conducted by UPSC for the Post of Drugs Inspector (Medical Devices) in Central … WebSAMPLE MCQS FOR PRACTICE Sl. No. Questions 1 The types of registers for registration of Pharmacists so far are : a) 5 b) 1 c) 3 d) 4 2 The D & C act consists of : a) 2 schedules …
Mcq on cdsco
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Web21. Which of the following is responsibility of state authority of CDSCO a. Regulatory control over the import of drugs b. Approval of new drugs and clinical trials c. Meetings of Drugs … Web30 sep. 2024 · The Central Drugs Standard Control Organization (CDSCO) is the Central Drug Authority for discharging functions assigned to the Central Government under the …
Web3. CDSCO action on IPC reported Cases; Welcome To DrugsControl.org " Human Rights aren't just about violence and terrorism. Unsafe drugs too fall into the category. The National Human Rights Commission (NHRC) has described the manufacture, distribution and sale of unsafe drugs and medical devices as a violation of human rights. " Read More Web25 dec. 2024 · 22. • In US following 4 types of applications are submitted for approval of drug for marketing depending upon the type and nature of the drug: A. New Drug …
WebFINAL YEAR UNIVERSITY EXAMINATION 2024-2024 Final Year B.Pharm. Semester VIII SUBJECT-BPH_E_808_T-Pharmacovigilance MULTIPLE CHOICE QUESTIONS: … WebTest: Internet Protocol - 1 fork Class 10 2024 is part of Classify 10 processing. The Test: Internets Protocol - 1 questions and answers have been prepared according to the School 10 exam syllabus.The Test: Internet Protocol - 1 MCQs are made for Classes 10 2024 Exam. Find important interpretations, questions, notes, meanings, examples, exercises, …
Web2 nov. 2024 · Essentially, CDSCO Approval for Drug manufacturing in India serves as a mandatory legal permit. The drug manufacturing license is accorded by the Central License Approving Authority (CLAA).Those lacking a production facility can secure a loan license to outsource the drug manufacturing drugs to a third party.
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