Thursday, 19 December 2013

BATCH :

A quantity of any drug produced during the given cycle of manufacture.

BATCH NUMBER :

designation printed on the label of the drug that identifies the batch and permit the production history of the batch, including all stages of manufacture and control, to be traced and reviewed.

COUNTERFEIT DRUG:

means a drug the label or outer packing of which is an imitation of ,or resembles or so nearly resembles as to be calculated to deceive the label or outer packing of a drug of another manufacture.

EXPIRY DATE :

means the date stated on the label of the drug after which the drug is not expected to retain its claimed efficacy,safety,quality or potency or after which it is not permissible to sell the drug.

Expert:

a specialist through university education and experience in the relevant field.

GENERIC NAME :

means the non-proprietry , scientific or official name of a drug as approved by the federal government

 LABEL:

a display of written, printed or graphic matter upon the immediate container , or the outside container or a wrapper of a drug package.

LABELING:

means all labels and other written , printed and graphic matter accompanying any drug .



 SCHEDULES



SCHEDULE A : Forms according to Punjab Drug Rules 2007
SCHEDULE B : Narcotic, Psychotropic , Antidepressant , and other controlled drugs e.g; 
                           Morphine,  cannabis, Amphetamine
SCHEDULE C : List of test e.g; physical examination,biological assays 
SCHEDULE D : Drugs that are to be sold by the retailer strictly under the prescription of 
                            registered  practitioner e.g; Bacitracin , Griseofluvin , erythromycin
SCHEDULE E :  List of poisons e.g ; Acetanilide , Conine 
SCHEDULE F :  List of minimum Requirments for a pharmacy

 FORMS ACCORDING TO FEDERAL DRUG LABORATORY AND FEDERAL GOVERNMENT ANALYST

Form 1: Regarding person not to dispose of stock in his possession

Form 2: Receipt for stock of drugs seized according to The Drug Act 1976

Form 3: Intimation of person form whom the sample is taken

Form 4; Memorandum to government analyst

Form 5: Memorandum to federal labortaory

Form 6: Certificate of test of analysis by the federal drug laboratory/ Government Analyst

LIST OF FORM ACCORDING TO PUNJAB DRUG RULES 2007

Form 1 : Monthly report from inspector shows inspection report of the month

Form 2: Report of drug testing laboratory shows progress report of the month 

Form 3:  Regarding person not to dispose of stock in his possession

Form 4 : Intimation of purpose to person from whom the sample is taken

Form 5 : Receipt for stock and articles seized under section of the drug act1976

Form 6: Memorandum to government analyst

Form 8(A): Application for the license to sell, store,exhibit for sale and distribute drugs by way of pharmacy

From 8(B): Application for the license to sell ,store,exhibit fro sale and distribute drugs by way of medical store    excluding the drugs specified in schedule G

Form 9 : License to sell drugs in pharmacy

Form 10 :  License to ell drugs in medical store



 


Tuesday, 17 December 2013

Rules And regulation for import of drugs



  1.  Federal government make rules for the ease of public and inform them by notifying in official gazette that certain t

  2. Federal government will deal with the import of drugs and to perform its function makes rules and issue directions to the importer and exporter

  3. ypes of drugs  that are mentioned in a official gazette imported or exported only under the license of licensing authority or by an exporter , importer or indentor

  4. some specified types of drugs are not  imported  by the importer ,they are allowed to import through an agency of government

  5. prohibit the import and export of drugs that are specified in the official gazette

  6. only such drugs are imported which are on sale in the market of any of the western countries USA,Japan,Australia or countries that are specified.

Saturday, 14 December 2013

ADULTERATED DRUGS :


according to drugs act 1976 adulterated drug means a drug ...



which consists in whole or in part of any filthy,putrid or decomposed substance or which contains any foreign matter vermin ,worms rodents or insects or

 which has been manufactured ,packed or held under unsanitary conditions whereby it has been contaminated with dirt ,filth or another foreign matter or whereby it may  have been rendered injurious to health or

the container of which releases any poisonous or deleterious substances which may render the contents injurious to health or

which bears or contains as an ingredient a substance other than the prescribed substance

with which any substance has been mixed or packed so as to reduce its quality or strength or for which any substance has been substituted wholly or in part ;