加拿大外贸
大家好！我是做蚊香出口的，刚入行不久。
好不容易联系到了孟加拉一个客户对我们的产品感兴趣。人家需要填申请农药登记证的信息。
对这个材料我是似懂非懂。不知道是否有朋友能帮帮忙，或者之前做过类似的农药证申请书的。
大家帮忙看看啊！
THE BANGLADESH GAZETTE, EXTRA, NOVEMBER16, 1985
FORM 1
(See rules 3)
Application for registration of Pesticides
1. Name and address of the applicant
:
2. Name of the pesticide
:
(Brand Name /Trade name)
3. Name and address of the manufacturer/ formulator
:
4. Common Name /Descriptive name
:
5. Chemical Name
:
(IUPAC nomenclature)
6. Structural formula
:
7. Empirical formula and molecular weight
:
8. Manufacturer’s development code number(s)
:211302
9. Active ingredient (certified percentage of active material)
(a)
Physical state
:
(b)
Colour /Appearance
(c)
Odour
:
(d)
Refractive index
:
(e)
Melting Point
:
(f)
Decomposition point
:
(g)
Viscosity
:
(h)
Boiling point
:
(i)
Vapor pressure: Figure should be given at a stated
Temperature preferably in the range of (20-25°C)
:
(j) Flash point
:
(k)Specific gravity/Density (for liquid only)
:
(l)Hydrolysis rate under stated relevant conditions
:
(m)Surface tension
:
(n) Stability
:
(o)
Solubility
:
(p)
Compatibility
:
(q) Photolysis
:
(r)Absorption spectra, e.g. Ultra violet, visible and
infrared, etc.
:
(s) Any other relevant properties
:
(t)
Acidity /Alkalinity /PH value
:
10. Technical grade material:
(a)Source: name and address of manufacturer and
address where manufactured
:
(b) Physical state
:
(c)
Colour
:
(d) Odour
:
(e)Acidity /Alkalinity or PH value
:
(f)Specific gravity
:
(g)Viscosity
:
(h)Flash point
:
(i) Minimum (and maximum) active ingredient
content in % W/W
:
(j)
Identity and amount of isomers, impurities and
other by products, together with information
on their possible range expressed as % W/W.
:
(k)
Storage stability ( Low and High
Temp. storage stability ).
:
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11. Formulated product:
(1) Identity /Appearance (colour) :
(2) Odour :
(3) Type of formulation :
(4) Content of active ingredient (s) :
(5) Content and nature (identify if possible of :
other components included in the formulation ,
e.g., technical grade, adjuvants and
inert ingredient.
(6)Water content /Moisture (above relevant) :
(7)Specific gravity :
(8)Viscosity :
(9) Low and High temp. storage stability :
(in respect to composition and
physical properties related to use .
(10) Impurities :
(11) Flamability:
(a) Liquid: Flash point :
(b)Solid: A statement must be made :
as to whether the product in flammable
(12) Acidity :
(13)Alkalinity :
(14) PH Value :
(15)Other properties may in certain :
case need evaluation
(16) Carrier Materials :
(17) Wetability ( for dispersible powers ) :
(18)Persistent foam ( for formulation :
applied in water )
(19)Suspensibility ( for dispersible powders :
and suspention concentrates)
(20).Particle size :
(21) Wet sieve test ( for dispersible powders :
and suspension concentration).
(22) Dry sieve test (for granules, dust) :
( 23)Emulsion stability (for emulsifiable :
concentrates)
(24) Bulk density :
(25) Corrosiveness (when necessary) :
(26) Flowability :
(27)Incase of Tablet /Pellets
(a)Weight :
(b) Thickness /height :
(c) Diameter :
(d) Colour /appearance :
(e) Percentage of active in gradients :
and other related standard specification
(28) Known incompatibilities with other :
products, e.g. pesticides, fertilizers
(29) Application with dossage rate :
12. Rate of release of active ingredient :
(granules, dust ,etc ).
13. Efficacy :
Primary evaluation date using, harmonized method
and reported in a systematically
presented complete dossier. :
(14) Toxicology data:
(a) Acute
Oral toxicity and dermal toxicity :
(b) Acute
Percentaneous toxicity :
(c) Acute
Inhalation :
(d) Acute
Other routes e.g. in traperitoneal :
(e)Skin irritation
(f) Eye irritation :
(g) Short term
Oral administration :
(h)Short term
Sensitizing effects :
(i)Toxic effect of metabolies, breakdown
Products or impurities :
(j) Metabolic -studies :
(k) Long –term toxicity, including carcinogenicity :
(l) Neurotoxicity :
(m)Reproduction studies :
(n)Embryotoxicity, including teratogenicity. :
(o)(Nutagenicity ) :
(p)Potentiation :
(q)Direct observation, e.g. clinical cases :
(r) Health record, both from industry and
agriculture. :
(s)Treatment of poisoning :
(t) First aid measure :
(u)Supplementary treatment :
(v)Waiting period
(Last application to harvesting) :
15. Residue studies:
(a) Primary physical, chemical and biological data :
(b)Identification of residue-design of
analytical method.
(c) Reliable residue data from supervised trials :
(d)Estimation of maximum residue level at harvest:
(e) Data on further disappearance on
storage, transport, etc :
(f)Estimation of residue level in commodity on sale :
(g)Data on disappearance on food :
preparation, cooking, or processing
(h) Prediction of potential consumer :
intake, actual intake studies
(i) Assessment of actual consumer intake :
(j) Persistence of the product :
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16. Prediction of environment effects:
(a) Fate and mobility studies of toxicant :
(b) Method of application of pesticide :
(c) Time of application :
(d)Rate of application :
(e)Scale of use (number of application etc) :
(f) Climatic and geographical locality :
(g)Volality of product :
(h) Water solubility :
(i) Octanol water partition coefficient :
(J)Absorption :
(k)Desorption :
(l)Degradation :
(m)Persistence :
(n) Effects on birds :
(o)Effects on fish :
(p)Effects on fish food species
(q)Effects on honey bees
(r) Degradation product in soil :
(s) Possibilities of accumulation, with
stable lipophilic compounds :
(t)Effects on local aquatic species :
(u)Effects on soil organisms :
(v) Disposal of used, condemned and surplus pesticides and
pesticides containers . :
(w) Proposal for labeling and directions for use :
17. Packaging:
(a)State weight (or for liquids, volumes) and the size of
package in which the products is to be marketed and for each size ,
the type of package, for instance i.e. ,1kg in cans with screw plug
and 50 kg in iron drums .( please note that the product must be sold only
in the package size and type noticed to the plant protection wing ,
Deptt. of Agriculture Extension and for which the label is approved) :
(b)Classification during transport.
18. Method of analysis:
(a) Methods to determine the active ingredients of the product
(the accuracy of the method of determination should be stated both in
instrumental and chemical ).
(b)Methods to determine the amount of isomers,
impurities and other bi-products .
19. Labeled sample for analysis:
(a)Analytical reference standard 2-5g.
(b)Technical grade material 0.5- 1.0 Kg
(c)Formulated products 5kg /lit for each formulation.
20. Registration fee:
Taka 2000 (Taka two thousands) to be deposited in Treasury Challan payable under Head of Account “………………………………………………”
I do hereby apply for registration of the pesticides particulars of which are given above and hereby certify that these particulars are to the best of my knowledge true and correct.
Explanation –In this Form, “Active ingredient” means an ingredient capable in itself of preventing ,destroying ,repelling or mitigating insects , fungi ,bacteria, nematodes various ,rodents, weeds or other pests when used in the same manner and for the same purpose and those for which it is intended but is not antagonistic to the activity of any other active ingredient in the same formulation .
Date ………… ……………………………………
Signature of applicant
Notes
Direction for completion and submission of application (In triplicate)
The application must be accompanied by :
(a)General literature of the product including toxicological and efficacy data.
(b)Standard specification of technical product and formulation of product .
(c)Statement of ingredient (active and inert materials to be enclosed separately in
a sealed and confidential cover ).
(d)Composition of formulation in details with percentage.
Certified true copy of the contract /agreement made between manufacturer /principal and the local agent authenticated by the competent agency of the country for import and marketing the product in Bangladesh.
3.
(a) In case of renewal of an existing registration, the previous certificates of registration:
and
(b)A suitable sample of the pesticide sufficient for test and analysis (Physical and
chemical properties)
4. Treasury Challan or Taka two thousand evidencing payment shall be deposited under the
receipt head: “…………………………………………..”
5. Submission of application in a sealed cover and marked “Confidential”
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建议你将这份英文版注册申请书翻译成中文，然后拿给你们公司的研发实验室或化验实验室的同事看，他们应该可以给你很大的帮助的！
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