Carcasses or viscera designated for pharmaceutical purposes shall be held in a vessel labelled "FOR PHARMACEUTICAL PURPOSE" and sealed under the supervision of the veterinary meat inspector before they are delivered to the pharmaceutical manufactory.

Carcasses or viscera having passed the post-mortem inspection, but later undergone degeneration, decay, contamination or any other changes that might endanger human health, shall be re-interpreted as "fail".

The slaughterhouse shall dispose the carcasses or viscera interpreted as "fail" using any of the following methods:
1.Rendering: After the approval of the veterinary meat inspector, carcasses or viscera may be delivered to a rendering site or a temporary storage site in transit to the rendering site.
2.Incineration or burial: Carcasses or viscera shall be denatured under the supervision of the veterinary meat inspector and then be delivered to an incineration or landfill site, or a temporary storage site in transit to the incineration or landfill site.
3.Other necessary actions as specified by the central competent authority.
The term "denature" stated in the preceding paragraph means cutting or chopping the carcasses or viscera into pieces and mixing them with a substance designated by the competent authorities to change their appearance or nature and to render them unusable for food.
For livestock or poultry interpreted as "fail" in ante-mortem inspection or carcasses or viscera interpreted as "fail" in post-mortem inspection may be denatured by injection with the aforesaid substance.

For the purpose of research or disease diagnosis, the academic and research institutions may apply to the central competent authority for the collection of specimens of carcasses/viscera deemed as "fail", having parasites and fetus. The aforesaid specimens shall not be moved out of the premises of slaughterhouse without a release permit issued by the veterinary meat inspector.