When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Central Drugs Standard Control Organisation - Wikipedia

    en.wikipedia.org/wiki/Central_Drugs_Standard...

    cdsco.gov.in and www.cdscoonline.gov.in The Central Drugs Standard Control Organisation ( CDSCO ) is India 's national regulatory body for cosmetics , pharmaceuticals and medical devices . It serves a similar function to the Food and Drug Administration (FDA) of the United States or the European Medicines Agency of the European Union .

  3. Drugs Controller General of India - Wikipedia

    en.wikipedia.org/wiki/Drugs_Controller_General...

    Analysis of Cosmetics received as survey samples from CDSCO (central drug standard control organisation) With the notification of Medical Device Rules 2017 by the Government of India, DCGI will also act as Central Licensing Authority (CLA) for the medical devices which fall under the purview of these rules.

  4. Type approval - Wikipedia

    en.wikipedia.org/wiki/Type_approval

    Type approval or certificate of conformity is granted to a product that meets a minimum set of regulatory, technical and safety requirements. Generally, type approval is required before a product is allowed to be sold in a particular country, so the requirements for a given product will vary around the world.

  5. Certificate of pharmaceutical product - Wikipedia

    en.wikipedia.org/wiki/Certificate_of...

    The certificate of pharmaceutical product (abbreviated: CPP) is a certificate issued in the format recommended by the World Health Organization (WHO), which establishes the status of the pharmaceutical product and of the applicant for this certificate in the exporting country; [1] it is often mentioned in conjunction with the electronic Common Technical Document (eCTD).

  6. ISO 13485 - Wikipedia

    en.wikipedia.org/wiki/ISO_13485

    ISO 13485 Medical devices -- Quality management systems -- Requirements for regulatory purposes is a voluntary standard, [1] published by International Organization for Standardization (ISO) for the first time in 1996, and contains a comprehensive quality management system for the design and manufacture of medical devices.

  7. Validation and verification (medical devices) - Wikipedia

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

    To establish a reference range, the Clinical and Laboratory Standards Institute (CLSI) recommends testing at least 120 patient samples. In contrast, for the verification of a reference range, it is recommended to use a total of 40 samples, 20 from healthy men and 20 from healthy women, and the results should be compared to the published reference range.

  8. Drugs and Cosmetics Act, 1940 - Wikipedia

    en.wikipedia.org/wiki/Drugs_and_Cosmetics_Act,_1940

    The term "drug" as defined in the act, includes various substances, diagnostic, and medical devices. The act defines "cosmetic" as any product that is meant to be applied to the human body for the purpose of beautifying or cleansing. The definition however excludes soaps. In 1964, the act was amended to include Ayurveda and Unani drugs. [2]

  9. Medical certificate - Wikipedia

    en.wikipedia.org/wiki/Medical_certificate

    A medical certificate can also be obtained online through telemedicine platforms, such as MedBond, which offer authentic medical certificates. An aegrotat (/ ˈ iː ɡ r oʊ t æ t /; from Latin aegrotat 'he/she is ill') [5] or 'sick note' is a type of medical certificate excusing a student's absence from school for reasons of illness.

  1. Related searches cdsco certificate for medical devices form pdf free 5 18 new 3 7 dodge engine

    cdsco manufacturers listcdsco authorized representative
    cdsco authorized agent