FEED REFERENCE STANDARDS |
CHAPTER IX LAWS REGULATING THE FEED INDUSTRY FEED LAW In in the Philippines, as in other countries, the feed control program has three phases: laws, regulations and administrative procedures. But the three are so closely tied together that they cannot be separated in the discussion of the various measures for safeguarding feed users. The major provisions of the feed law are as follows:
To upgrade the quality of medicated and commercial feeds, the BAI has been mandated to implement the following laws and regulations: 1. R.A. 1556, as amended, otherwise known as the "Livestock
and Poultry Feeds Act," and its implementing rules and regulations (Animal
Industry Administrative Order Nos. 35, 35-A and 40; and General Memorandum
Order No. 1);
The above-mentioned laws and regulations are administered and implemented by the Secretary of Agriculture through the Director of Animal Industry. The BAI, through its Animal Feed Standards Division (AFSD), oversees the manufacture, importation, distribution, advertisement and sale of livestock, poultry, aqua and specialty feeds, veterinary drugs, and chemical feed additives. The Department of Agriculture and the Department of Health signed a Memorandum of Agreement to delineate the responsibilities regarding registration of veterinary drugs and products. R.A. 3720, as amended by Executive Order No. 175, defines veterinary drzigs andproducts as "any substance, including biological products, applied or administered to food-producing, companion, aquatic, laboratory and exotic animals, whether used for therapeutic, prophylactic or diagnostic purposes or for medication of physiologic functions or behaviors." This law is comprehensive and all-embracing than R.A. 1556, as amended, when it comes to coverage, registration and quality control procedures. CLINICAL TRIALS OF VETERINARY DRUGS
REGISTRATION AND LICENSING
No change in the brand of a registered feed/veterinary dru- can be made without a written notification to the proper authorities. The Director of Animal Industry is empowered to caiicel the registration of any feed/veterinary drug that does not conform to the provisions of those aforementioned laws (i.e., labeling and quality standards). INSPECTION AND SAMPLING
Analytical methods for feed evaluation are also carefully prescribed.
R.A. 1556, as di-nended, mandates that the government and private feed
laboratories shall adopt the methods of analysis published in the official
methods of Analysis of the Association of Official Agricultural Chemists
(AOAC) in evaluating the quality of animal feeds. This is another provision
for uniformity, as well as accuracy.
Feed samples are analyzed for their nutrient composition (minimum percentage of crude protein and crude fat, ash, mineral and moisture), purity (absence or presence of adulterants and other extraneous materials, which are harmful to livestock or man) and toxicity (by using experii-nental animals). Results of the analysis are returned to the AFSD for proper decoding and interpretation. Decoded results are used to monitor the different feed mills or fari-ns. Feeds failing below minimum standards or substantially below guarantees and containing substances injurious to the animals, may be condemned and impounded. In cases of willful or repeated violations of the law, the registration certificates of errin(' persons or entities may be temporarily suspended or cancelled, depending oil tile degree of tile violations. Persons responsible for such violations may also be prosecuted. Laws regulating the compound feed industry are as vibrant and dynamic as the industry itself. They do change, depending on the needs of the industry; but the change is always for the better. For after all, these laws are specifically designed to safeguard everyone - the producer, trader, end-user and, ultimately, the consuming public. |