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  2. FDA Center for Devices and Radiological Health - Wikipedia

    en.wikipedia.org/wiki/FDA_Center_for_Devices_and...

    The MDA established a risk-based framework for the classification of medical devices and a regulatory pathway for medical devices to get to the market, created a regulatory pathway for medical device clinical trials, and established several post-market requirements including manufacturer registration and device listing with the FDA, good ...

  3. Validation and verification (medical devices) - Wikipedia

    en.wikipedia.org/wiki/Validation_and...

    For instance, a regulatory agency (such as CE or FDA) may ensure that a product has been validated for general use before approval. An individual laboratory that introduces such an approved medical device may then not need to perform their own validation, but generally still need to perform verification to ensure that the device works correctly ...

  4. Validation (drug manufacture) - Wikipedia

    en.wikipedia.org/wiki/Validation_(drug_manufacture)

    Validation is a requirement of food, drug and pharmaceutical regulating agencies such as the US FDA and their good manufacturing practices guidelines. Since a wide variety of procedures, processes, and activities need to be validated, the field of validation is divided into a number of subsections including the following: Equipment validation

  5. BCS Examination - Wikipedia

    en.wikipedia.org/wiki/BCS_Examination

    The BCS Examination (Bengali: বিসিএস পরীক্ষা) is a nationwide competitive examination in Bangladesh conducted by the Bangladesh Public Service Commission (BPSC) for recruitment to the various Bangladesh Civil Service cadres, including BCS (Administration), BCS (Audit & Accounts), BCS (Taxation), BCS (Customs and Excise), BCS (Foreign Affairs), and BCS (Police) among ...

  6. National Medical Products Administration - Wikipedia

    en.wikipedia.org/wiki/National_Medical_Products...

    The medical devices regulatory system is based on regulations issued by the State Council, NMPA orders and NMPA documents that provide detailed rules for medical device registration and licensing practice. [10] Medical device type testing must be based upon the Chinese National Standard (Chinese: Guobiao, GB) or at least on an Industry Standard ...

  7. Bangladeshi intelligence community - Wikipedia

    en.wikipedia.org/wiki/Bangladeshi_intelligence...

    Major responsibilities of this branch are to meet up any intelligence required from government, registration and control of foreigners, perform verification role, give protection to the VIPs intelligence gathering, immigration controls etc. [3] [4] This is the only intelligence outfit of Bangladesh which works in all strategic, operational and ...

  8. Office of Criminal Investigations - Wikipedia

    en.wikipedia.org/wiki/Office_of_Criminal...

    The FDA regulates approximately 25 cents of every dollar spent annually by Americans, the FDA is responsible for regulating products to ensure the safety of food, drugs, biological products, medical devices, cosmetics, radiation-emitting devices, and more. The law enforcement arm of the FDA, the Office of Criminal Investigations.

  9. Government agencies in Bangladesh - Wikipedia

    en.wikipedia.org/wiki/Government_agencies_in...

    The Government agencies in Bangladesh are state controlled organizations that act independently to carry out the policies of the Government of Bangladesh. The Government Ministries are relatively small and merely policy-making organizations, allowed to control agencies by policy decisions.

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