Searching 'packaging' | Accredited Consultants Pvt Ltd in Noida

Chat with us

packaging

3.8 Design output means the results of a design effort at each design phase and at th ...

packaging

5. Sanitation: Availability of written specifications and procedures for cleaning the ...

packaging

(3) In case of imported diagnostic in vitro diagnostic medical devices, the report of ...

packaging

3.0 Labelling: The dossier should typically contain a complete set of labeling associ ...

7.5.1.1 General requirements The manufacturer shall plan and carry out production and service provision under controlled conditions. Controlled conditions shall include, as applicable:— (a) the availability of information that describes the characteristics of the product; (b) the availability of documented procedures, documented requirements, work instructions; and reference materials and refere ...

packaging

(ii) Evidence of the ongoing revalidation of the process should also be provided. Typ ...

packaging

4.0 Design and manufacturing information: 4.1 Device Design: The dossier should conta ...

FIFTH SCHEDULE [Refer rules 20(3), 20(5), 20(8), 22(i)] QUALITY MANAGEMENT SYSTEM FOR MEDICAL DEVICES AND IN VITRO DIAGNOSTIC MEDICAL DEVICES 1. General Requirements: 1.1 This Schedule specifies requirements for a quality management system that shall be used by the manufacturer for the design and development, manufacture, packaging, labelling, testing, installation and servicing of medical device ...