Pak Law
Indeed, it is compendium of the provincial and federal laws of Islamic Republic of Pakistan, compiled from the authentic sources of law agencies, private and public libraries including virtual and web ones; and are being published under my blog http://paklaws2014.blogspot.com/ for awareness to Pakistani Laws as well as access to justice in one touch. How much it is advantageous, your valuable comments will be awaited. Thanks.
Friday, 25 December 2015
Thursday, 3 December 2015
MARRIAGES VALIDATION ACT, 1892
l[THE MARRIAGES VALIDATION ACT, 1892]
ACT No. II OF 1892
[29th January, 1892]
An Act to validate certain marriages solemnized under Part VI of the Christian
Marriage
Act, 1872.
WHEREAS provision is made in Part VI of the Christian Marriage Act, 1872, (XV of
1872) for the solemnization of marriages between persons of whom both are Native Christians,
but not of marriages between persons of whom one only is a Native Christian;
Thursday, 5 November 2015
INVESTMENT COMPANIES AND INVESTMENT ADVISERS RULES, 1971
INVESTMENT COMPANIES AND INVESTMENT ADVISERS
RULES, 1971
(As amended upto 1st May, 1999)
CHAPTER I
PRELIMINARY
(ii) An investment purchased and awaiting payment
RULES, 1971
(As amended upto 1st May, 1999)
CHAPTER I
PRELIMINARY
(ii) An investment purchased and awaiting payment
Monday, 2 November 2015
Drugs (Labelling and Packing) Rules, 1986
The Drugs (Labelling and Packing) Rules, 1986
1. Short title and commencement: (1) These rules may be
called the Drugs (Labelling and Packing) Rules, 1986.
(2) They shall come into force on the expiration of the
period of one year beginning with their publication in the official Gazette.
2. Definitions: In these rules, unless there is anything
repugnant in the subject. or context; (a) "international non-proprietary
name" means the name of a drug as recommended by the World Health
Organization or such other name as may be notified by the Federal Government in
the Official Gazette;
(b) "pharmacopoeia" means a publication mentioned
in sub-clause (ii) of clause (z) of Section 3 of the Drugs Act, 1976 (XXXI of
1976);
(c) "pharmacopoeial name" means the name of a drug
as mentioned in the pharmacopoeia;
(d) "Schedule" means a schedule to these rules;
and
(e) "registered medical practitioner" means a
medical practitioner registered or provisionally registered under the Medical
and Dental Council Ordinance, 1962 (XXXII of 1962).
3. Manner of labelling: The following particulars shall
appear either in print or in writing in inedible ink in a conspicuous manner on
the label of the innermost container of a drug and also on the covering in
which such container is packed, namely :--
(a) the registered name of the drug;
(b) if the registered name is a proprietary name, then
immediately following the registered name, the generic name or other name, if
any, approved by the Registration Board, for this purpose small be printed
within breakets with at least equal prominence as that of the brand name;
(c) the international non-proprietary name or the
pharmacopoeial name or the generic name, and if no such name is known, the
chemical name, of each active ingredient of a drug with weight or measure in
metric system, or the number of units of activity, as the case may be,
expressed,--
(i) in the case of oral liquid preparations, in terms of
contents per specified volume,, the volume being indicated in millilitres;
(ii) in the case of liquid parenteral preparations ready for
administration, in terms of millilitres or percentage by volume or dose:
Provided that in the case of a preparation contained in
ampoule, it, shall be sufficient if the ingredients are shown on the label or
warpper affixed to any package in which such ampoule is issued for sale:
(iii) in the case of drugs in solid form intended for
parenteral administration, in terms of weight or unitage, per milligram or gram
or per container;
(iv) in the case of tablets, capsules, pills and the like,
in terms of the contents per tablets, capsule, pill or other unit, as the case
may be; and
(v) in the case of other preparations, in terms of
percentage by weigh or volume or unitage, per gram or millilitre, as the case may
be;
(d) the name and principle place of business of the
manufacturer;
(e) the drug manufacturing licence number;
(f) the drug registration number;
(g) the date of expiry;
(h) Urdu version of the following namely:-
(i) registered name of drug.
(ii) dosage (numerals in English shall be sufficient ): and
(iii) Instructions.
(i) the distinctive batch number, date of manufacture, and
the maximum retail price:
Provided that in the case of a drug packed in a strip of
paper, or blister or foil, or contained in an ampoule of a capacity of not more
than two millilitres or in an ampoule containing a sterile suture or ligature,
and such strip, foil. blister, or ampoule is placed in another package, and
also in the case of printed collapsible tubes, it shall be sufficient to give
the information on the outer packing containing such strip, foil, blister or
ampoule:
Provided further that the Registration Board may allow
relaxation of any of these conditions.
4. Labelling of drugs for internal use: The label of
container of a drug meant for internal use, except a drug contained in a strip
or foil or blister or collapsible tube, shall, in addition to the particulars
required to be given under rule 3, bear in a conspicuous manner,--
(i) If it contains a substance specified in the Schedule,
the words "To be sold on prescriptions of a registered medical
practitioner only"; and
(ii) if it contains not less than three per cent by volume
an alcohol, a statement giving the quantity of alcohol in terms of average percentage
by volume of absolute alcohol in the finished product.
5. Labelling of drugs for external use only: The label of a
container of ointment, cream, liniment, lotion, liquid, antiseptic or any other
drug for external application shall, in addition to the particulars required to
be given under rule 3, bear in a conspicuous manner,--
(i) the words "For external use only"; and
(ii) if the drug contains a substance specified in the
Schedule, the words "Poison; for external use only".
6. Labelling of physician's samples: The label of a
container of every drug intended for distribution to the medical profession as
free sample shall, in addition to the particulars required to be given under
these rules, bear the words "Physician's sample: Not for sale" which
shall be overprinted or stamped: Provided that if the drug is packed in a strip
of paper or blister or foil or contained in an ampoule of a capacity of not
more than three millilitres or in a collapsible tube, it shall be sufficient to
label the outer packing only with the said words.
7. Labelling of drugs for Government supply: The label of a
container of every drug intended for the supply to any Government agency
including an autonomous body or a semi-Government Agency shall, while complying
with the other labelling requirements of these rules, bear the words or mark
reading "Government Supply" or such other words or mark as may be
required by the agency concerned.
8. Labelling of drugs for veterinary use: The label of a
container of drug for veterinary use shall bear in a conspicuous manner,
preferably in red ink the words for veterinary use only.
9. Outer transparent wrapper not to require labelling:
Nothing in these rules shall be deemed to require the labelling of any
transport cover, wrapper, case or other covering used solely for the purpose of
packing, transport or delivery of a drug.
10. Labelling of non-sterile surgical ligature and suture:
Every container of, and every wrapper enclosing a surgical ligature or suture,
other than a ligature or suture certified to be sterile and fit for surgical
use without further sterilization, shall bear a label on which shall be printed
or written in a conspicuous manner in indelible red ink the word
"Non-sterile surgical ligature/suture: Not to be used for operation upon
human body unless properly sterilized".
11. Use of letter to indicate specifications: If a drug is
included in the recent edition of any publication specified in the rules, the
name of relevant publication in conventional abbreviations (B.P., U.S.P., etc.)
shall be printed in indelible ink, on the label to indicate that the drug
conforms to the specifications set out in that publication.
12. Packing of finished drugs: Each finished drug ready of
use-shall be packed in containers intended for retail sale to a hospital,
.dispensary, clinic or any other such institution.
13. Labelling of drugs manufactured for export or
experimental purposes: (1) Nothing contained in rules 3 to 12 shall apply to a
drug manufactured for experimental purposes which shall be labelled in
accordance with rule 23 of the Drugs (Licensing, Registering and Advertising)
Rules. 1976.
(2) Labelling of drugs manufactured for export shall, in
addition to meeting specific requirements of the importers, bear following
particulars printed in indelible ink, on the inner most container and other
packings of such drugs,--
(i) name of drugs ;
(ii) name and address of manufacturer; and
(iii) batch number and dates of manufacture and expiry date
of the drug:
Provided that in case of a drug packed in a strip of paper,
foil or blister or contained in an ampoule of a capacity of not more than two
millilitres or in a printed collapsible tube or in an ampoule containing a
sterile suture or ligature and that such strip, foil, blister or ampoule is
placed in another package, then it shall be sufficient to give name, date of
expiry and batch number of the drug, name and address of the manufacturer on
the inner-most container or its label, while full particulars shall be given on
outer packing containing such strip, foil, blister, ampoule or tube.
14. Exemption: These rules shall not be applicable in
respect of a drug made up ready for treatment, whether after or without
dilution and is supplied by a person licensed to sell drugs on the prescription
of a registered medical practitioner.
Provided that the label bears the following particulars,
namely :--
(i) the ham e and address of the suppliers of the drug;
(ii) the name of the patient ;
(iii) the number representing the serial number of the
entries in the prescription register;
(iv) if the drug is for internal use, the dosage;
(v) if the drug is for external use, and does not contain a
substance specified in the Schedule' the words "For external use
only"; and
(vi) if the drug is for external use and contains a
substance specified in the Schedule, the words "Poison: for external use
only".
THE SCHEDULE
TO BE SOLD BY A RETAILER ON THE PRESCRIPTION OF REGISTERED
MEDICAL PRACTITIONER
1. C.N.S. stimulants.
2. Drugs affecting uterine motility.
3, Drugs inhibiting hormonal production.
3. Hormones and other steroidal preparation excluding
preparations for external and topical use.
5. Narcotic drugs as per Single Convention on Narcotic
Drugs, 1961.
6. Psychotropic substances mentioned as per Convention on
Psychotropic Substances, 1971.
Friday, 30 October 2015
SINDH PROVINCE PENSION FUND (AMENDMENT) ACT, 2006
PROVINCIAL ASSEMBLY OF SINDH
N O T I
F I C A T I O N
Karachi, the 18th December, 2006
NO.PAS/Legis-B-7/2006-. The Sindh Province Pension Fund (Amendment)
Bill, 2006 have been
passed
by the Provincial
Assembly of Sindh on Wednesday, the 15th November, 2006 and assented to by the Governor of Sindh
on Thursday, the 14th December, 2006 is hereby published as an Act of the Legislature of Sindh.
THE SINDH PROVINCE
PENSION FUND (AMENDMENT) ACT, 2006
SINDH ACT NO.VI OF 2006
(First published after having
received the assent of
the Governor of Sindh
in the
Gazette of Sindh (Extra-Ordinary) dated18th December 2006).
AN ACT
to amend the Sindh Province Pension
Fund Ordinance, 2002.
Preamble WHEREAS it is expedient to amend the
Sindh Province Pension
Fund Ordinance,
2002, in the manner hereinafter appearing;
Thursday, 29 October 2015
PUNJAB PRIVATE EDUCATIONAL INSTITUTIONS (PROMOTION AND REGULATION) ORDINANCE, 1984
[1]THE PUNJAB PRIVATE EDUCATIONAL INSTITUTIONS
(PROMOTION AND
REGULATION) ORDINANCE, 1984
( IV of
1984)
[12thAugust,
1984]
An
Ordinance
to provide for the
promotion and regulation of private educational institutions.
Preamble.— WHEREAS it is expedient to promote and regulate the
setting up and management of private educational institutions in the Punjab;
NOW,
THEREFORE, in pursuance of the proclamation of the 5th day of July,
1977, read with the Laws
(Continuance in Force) Order, 1977, (CMLA Order No. 1 of
1977), and the Provisional Constitution Order, 1981, (CMLA
Order No. 1 of 1981), the Governor of the Punjab is pleased to make and
promulgate the following Ordinance:-
Tuesday, 27 October 2015
RESTRICTION OF HABITUAL OFFENDERS (PUNJAB) ACT, 1918
[26 April 1918]
An
Act for restricting the movements of habitual offenders in the Punjab and for
requiring them to report themselves.
WHEREAS it is expedient
to make provision for restricting the movements of habitual offenders in the
Punjab and requiring habitual offenders in the Punjab to report themselves, and
whereas the previous sanction of the Governor-General in Council has been
obtained under section 79(2) of the Government of India Act, 1915, to the
passing of this Act:
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