আবেদন শুরুর তারিখ:
24 এপ্রিল, 2022
আবেদনের শেষ তারিখ:
15 মে, 2022
মোট দেখেছেন: 342
জব আইডি: #GJOB3103
প্রকাশের তারিখ: 24 এপ্রিল, 2022
শেষ তারিখ: 15 মে, 2022
টেলিটক জব নিয়োগ প্রক্রিয়াটির কোনও পর্যায়ে কোনও ফি নেওয়া হয় না.
দয়া করে নোট করুন যে টেলিটক জব একটি সমান কর্মসংস্থান সংস্থা। প্ররোচনার যে কোনও রূপ প্রার্থীর পক্ষে অযোগ্য ঘোষণা করবে।.
পদ্ধতি প্রয়োগ করুন
আবেদনের শেষ দিন: 15 মে, 2022
প্রতিষ্ঠানের নাম: strengthening Of Drug Administration Management SDAM
সংক্ষিপ্ত নাম: SDAM
বিস্তারিত দেখুন: History Historical background Before 1971 -An organization under the Central Govt of Pakistan under the Controller of drugs. After the war of liberation- An attached department of the Ministry of Health and Population Control. Since 1976 -A separate Directorate directly under the Ministry of Health and Family Welfare, 17 January 2010 upgraded as the Directorate General of Drug Administration. Introduction Directorate General of Drug Administration (DGDA) is the organization entrusted with the responsibility of ensuring the quality, efficacy and safety of pharmaceutical products though the implementation of relevant legislation. The organization is trying its best to fulfill the requirements of the pharmaceutical sector of the country and thereby meeting the needs of the people of the country by ensuring the safety, efficacy and quality of the medicines. Responsibility The responsibilities of this organization are as follows : a. To ensure the quality, safety, efficacy and usefulness of all kinds of drugs and medicines including Homeopathic, Unani, Ayurvedic and Herbal drugs which are produced , imported and marketed in the country and also exported to overseas. b. To make essential drugs available and affordable to the common people of the country. Drug Testing Laboratory Testing of drugs are required for evaluating pre-registration and post-marketed drugs and medicines quality. At present, there are two Govt. Drug Testing Laboratories in the country, one unit in Chittagong and another in Dhaka. Legislation All the activities of DGDA are governed & guided by * The Drug Act 1940 * The Drug Rules 1945 and their amendments * The Drug Rules 1946 and their amendments * The Drug (Control) Ordinance 1982 and its amendments * The Drug (Control) Ordinance Amendment Act 2006 * National Drug Policy 2016 The Ordinance provides for the following legislative powers and responsibilities with respect to drugs and medicines: 1. Formation of a Committee of experts, called the DCC or Drug Control Committee, for consideration of registration of medicines and/or their cancellation. 2. Prohibition of manufacture and sale of drugs without the supervision of pharmacists. 3. Restriction on import of certain pharmaceuticals and finished drugs. 4. Review of under-licensing agreements. 5. Fixation of prices of essential drugs. 6. Control of advertisements and claims in respect of drugs. 7. Implementation of GMP in the manufacturing units as recommended by WHO. 8. Formation of Drug Courts for trying offenses related to drugs. 9. Formation of a National Drug Advisory Council for advising the Govt. on matters related to essential drugs. 10. Formation of an Appellate Authority. 11. Recognition of Traditional and Homeopathic medicines as drugs. 12. Imposition of penalty for : - manufacture and sale of adulterated, spurious and restricted drugs. - manufacture and sale of substandard drugs. - unauthorized import of drugs and raw materials. - sale of medicines at prices higher than the Maximum Retail Price (MRP) by the Licensing Authority. - theft of Drugs from Govt. hospitals and stores. - illegal advertisement of drugs and claims about their qualities and uses. Major Function of DGDA 1. Evaluation of the proposals of new projects of all systems of medicines. 2. Issue and renewal of drug manufacturing licenses. 3. Issue and renewal of retail and whole sale drug licenses. 4. Registration and renewal of drug products. 5. Fixation of price and certification of price for drug products. 6. Inspection of pharmaceutical establishments 7. Approval of block list for the import of raw- and packaging materials. 8. Approval of indent for import of finished drugs. 9. Surveillance and pharmacovigillance activity 10. Prosecution of cases in the drug courts and other courts 11. Issue of export licenses, FSC (Free Sales Certificate), GMP (Good Manufacturing Practices) Certificate & CPP ( Certificate for Pharmaceutical Products.)http://dgda.gov.bd/