Approval for the Implementation of Preclinical Testing for Quasi-Drugs.

UMKU Detail

  • Parameter: All
  • Authority: Minister/Head of Agency

Requirements

  1. Evidence of paying PNBP

    2. Duration: -

  2. Standard Approval for Preclinical Testing of Traditional Medicines, Quasi-Medicines, Health Supplements, and Cosmetics.

    3. Duration: -

Responsibilities

  1. Conduct preclinical testing according to approved protocols and GLP standards.

    2. Duration: -

  2. Report any changes or amendments to the preclinical testing protocol.

    3. Duration: -

Sector: Drugs and Food.
Status: Available
Belongs to:
10799
11040
11090
20232
21012
21022
46334
46339
46441
46442
46443
47111
47112
47191
47724
47911
47999
72103
74117

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