Code of Alabama

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6-5-502
Section 6-5-502 Limitation periods for product liability actions. (a) All product liability
actions against an original seller must be commenced within the following time limits and
not otherwise: (1) Except as specifically provided in subsections (b), (c), and (e) of this
section, within one year of the time the personal injury, death, or property damage occurs;
and (2) Except as specifically provided in subsections (b), (c), and (e) of this section,
each element of a product liability action shall be deemed to accrue at the time the personal
injury, death, or property damage occurs; (b) Where the personal injury, including personal
injury resulting in death, or property damage (i) either is latent or by its nature is not
discoverable in the exercise of reasonable diligence at the time of its occurrence, and (ii)
is the result of ingestion of or exposure to some toxic or harmful or injury-producing substance,
element or particle, including radiation, over a period of time as opposed...
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2-23-3
Section 2-23-3 Permit required for manufacturing or distribution; fees. Every manufacturer
or distributor selling agricultural liming materials in this state shall, on or before October
1 of each year or prior to manufacture or distribution of such liming material in the State
of Alabama, apply for and obtain an annual permit for such purpose on a form to be furnished
by the commissioner. Such application shall be accompanied by a permit fee established by
the Board of Agriculture and Industries not to exceed two hundred fifty dollars ($250) and
shall show the brand name under which the liming material will be sold. If more than one type
of agricultural liming material is manufactured or distributed or the product or the brand
name is changed by a manufacturer or distributor, an additional permit fee established by
the Board of Agriculture and Industries not to exceed one hundred twenty-five dollars ($125)
for each additional brand or type of liming material must be paid. All permits...
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20-1-150
Section 20-1-150 Marking or imprinting of drug products in finished solid oral dosage forms
required. No drug product in finished solid oral dosage form for which a prescription is required
by federal law may be manufactured or commercially distributed within this state unless it
has clearly and prominently marked or imprinted on it an individual symbol, number, company
name, words, letters, marking, national drug code, or any combination thereof, identifying
the drug product and the manufacturer or distributor of the drug product. (Acts 1981, No.
81-389, p. 595, §1.)...
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22-11C-12
Section 22-11C-12 Liability under chapter. (a) No person shall have any claim or cause of action
against the State of Alabama, or its political subdivisions, or any individual arising out
of any acts or omissions which occurred under the provisions of this chapter, if the state,
political subdivisions, or individual is in compliance with this chapter. (b) No person shall
have any claim or cause of action against any person, or the employer or employee of any person,
who participates in good faith in the reporting or receiving, or both, of head or spinal cord
registry data or data for head or spinal cord injury morbidity or mortality studies in accordance
with this chapter. (c) No license of a health care facility or health care provider may be
denied, suspended, or revoked for the good faith disclosure of confidential or privileged
information in the reporting of head or spinal cord injury registry data or data for head
or spinal cord injury morbidity or mortality studies in accordance...
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22-13-35
Section 22-13-35 Liability under article. (a) No person shall have any claim or cause of action
against the State of Alabama, or its political subdivisions, or any individual arising out
of any acts or omissions which occurred under the provisions of this article, if the state,
political subdivisions, or individual is in compliance with this article. (b) No person shall
have any claim or cause of action against any person, or the employer or employee of any person,
who participates in good faith in the reporting or receiving, or both, of cancer registry
data or data for cancer or benign brain-related tumor morbidity or mortality studies in accordance
with this article. (c) No license of a health care facility or health care provider may be
denied, suspended, or revoked for the good faith disclosure of confidential or privileged
information in the reporting of cancer registry data or data for cancer or benign brain-related
tumor morbidity or mortality studies in accordance with this...
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6-12A-6
Section 6-12A-6 Penalties; unlawful practices. (a) Revocation of stamping privileges and civil
penalty. In addition to or in lieu of any other civil or criminal remedy provided by law,
upon a determination that a wholesaler, distributor, or any person has violated subsection
(c) of Section 6-12A-3, or any regulation adopted pursuant thereto, the commissioner may revoke
or suspend the stamping privileges of any stamping agent in the manner provided by Section
40-2A-8. Each stamp affixed and each offer to sell cigarettes in violation of subsection (c)
of Section 6-12A-3 shall constitute a separate violation. For each violation thereof, the
commissioner may also impose a civil penalty in an amount not to exceed the greater of 500
percent of the retail value of the cigarettes sold or five thousand dollars ($5,000) upon
a determination of violation of subsection (c) of Section 6-12A-3 or any regulations adopted
pursuant thereto. (b) Contraband and seizure. Any cigarettes that have been...
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8-21C-3
Section 8-21C-3 Manufacturer and dealer agreement - Required for sales by manufacturer or distributor.
(a)(1) After September 30, 2011, a manufacturer or distributor may not sell a recreational
vehicle in this state to or through a dealer without having first entered into a manufacturer
and dealer agreement with the dealer which has been signed by both parties. (2) A dealer may
not sell a new recreational vehicle in this state without having first entered into a manufacturer
and dealer agreement with a manufacturer or distributor which has been signed by both parties.
(b) The manufacturer or distributor shall designate the area of sales responsibility exclusively
assigned to a dealer in the manufacturer and dealer agreement. Except as provided in subsection
(c), the manufacturer or distributor may not review or change the area of sales responsibility
without the consent of both parties or contract with another dealer for the sale of the same
line-make in the designated area until at...
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8-21A-11
Section 8-21A-11 Supplier to indemnify dealer against claims relating to manufacture, assembly,
or design beyond dealer's control. The supplier will fully indemnify and hold harmless its
dealer against any losses, including but not limited to: court costs, reasonable attorney's
fees, any damages arising out of complaints, claims or lawsuits including, but not limited
to, strict liability, negligence, misrepresentation, warranty either express or implied, or
recession of the sale where the complaint, claim or lawsuit relates to the manufacture, assembly,
or design of new items covered by this chapter, parts, or accessories, or other matters relating
to the manufacturer, beyond the control of the dealer. (Acts 1991, No. 91-721, p. 1401, §11.)...

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34-23-11
Section 34-23-11 Physicians, dentists, registered nurses, etc., exempt from chapter. (a) Nothing
contained in this chapter shall prevent any licensed practitioner of the healing arts from
personally compounding, dispensing, administering, or supplying to his or her patient drugs
and medicines for their use. This chapter shall not apply to the manufacture or sale at wholesale
or retail of patent or proprietary medicines as purchased from a manufacturer or wholesaler,
or to the manufacture or sale at wholesale or retail of packaged, bottled, or nonbulk chemicals,
medicines, medical and dental supplies, cosmetics, and dietary foods when identified by and
sold under a trademark, trade name, or other trade symbol, privately owned or registered in
the United States Patent Office, sold or offered to be sold to the general public, if the
article meets the requirements of the Federal Food, Drug, and Cosmetic Act other than prescription
legend drugs. (b) A registered nurse in the employment of...
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6-12A-2
Section 6-12A-2 Definitions. For the purposes of this chapter, unless otherwise indicated,
the following terms shall have the meanings respectively ascribed to them by this section:
(1) BRAND FAMILY. All styles of cigarettes sold under the same trade mark and differentiated
from one another by means of additional modifiers or descriptors, including, but not limited
to, menthol, lights, kings, and 100s and includes any brand name (alone or in conjunction
with any other word) trademark, logo, symbol, motto, selling message, recognizable pattern
of colors, or any other indicia of product identification identical or similar to, or identifiable
with, a previously known brand of cigarettes. (2) CIGARETTE. As defined under subdivision
(4) of Section 6-12-2. (3) COMMISSIONER. The Commissioner for the Department of Revenue for
the State of Alabama. (4) DISTRIBUTOR. A person, wherever resident or located, who purchases
non-tax-paid cigarettes and stores, sells, or otherwise disposes of the...
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