Food and Drug Administration

Topics: Adverse drug reaction, Regulation, Pharmacology Pages: 4 (667 words) Published: August 26, 2013
Food and Drug Administration
Food and Drug Administration
General Functions
a. Develops plans policies, programs and strategies for regulating processed foods, drugs and other related products

b. Formulates rules, regulations and standards for licensing and accreditation of processed foods, drugs and other related products

c. Conducts licensing and accreditation of processed foods, drugs and other related products.

d. Provides technical, consultative and advisory services to and develops capability of filed offices on licensing and enforcement of laws, rules and regulations pertaining to processed foods, drugs and other related products.

e. Monitors, evaluates and ensures compliance of manufacturers, distributors, advertisers and retailers of processed foods, drugs and other related products to health rules and regulations and standards of quality.

f. Advises the Secretary and Undersecretary of Health on matters pertaining to regulation of processed foods, drugs and other related products.

1. Policy, Planning and Advocacy Division

Specific Functions

a. Develops plans, policies and programs pertaining to the regulation of processed foods, drugs and other related products.

b. Provides technical information and assistance to clients and the general public on matters pertaining to food and drug laws, regulations, functions and services.

c. Develops and maintains a database of all licensed/accredited processed foods, drugs and other related products.

d. Promotes rational drug use, self reliance and tailored procurement and monitors drug prices per Generics Law and the Philippine Drug Formulary

e. Conducts pharmaco-epidemiological and pharmaco-economic analysis.

2. Regulation Division I

Specific Functions

a. Conducts inspection and issues licenses for the operation of establishments involved in the importation, exportation, distribution and retailing of processed foods, drugs, medical devices, in vitro reagents,...
Continue Reading

Please join StudyMode to read the full document

You May Also Find These Documents Helpful

  • Federal Food, Drug, and Cosmetic Act of 1938 Research Paper
  • Essay about Food Regulations
  • Pharmacology: Food and Drug Administration and Prescription Drug Essay
  • Regulatory Agency: Food and Drug Administration Essay
  • Medication Administration Essay
  • Food Label Analysis Essay
  • Essay about History and Laws Behind the Federal Food and Drug Act of 1906
  • Essay about Prescription Drug

Become a StudyMode Member

Sign Up - It's Free