进口化妆品申报资料及要求英文版及宝贝计划婴儿用品专卖店计划书

ApplicationdossiersforadministrativelicensingofimportedcosmeticrequiredbySFDAPARTONE:ImportedcosmeticsclassificationTheimportedcosmeticsaredividedintotwomajorcategoriesbySFDA:importedcosmeticforparticularpurpose,andimportedcosmeticfornon-particularpurpose.ThedetaileddescriptionabouttheclassificationissetforthinAppendix3.PARTTWO:AdministrativelicensingofimportedcosmeticforparticularpurposeAdministrativelicensingofimportedcosmeticforparticularpurposeforthefirsttime,theapplicationdossiersshouldbeprovidedasfollows,(1)Applicationformofadministrativelicensingofimportedcosmeticforparticularpurpose,(2)ThereasonfornameoftheimportedproductsinChinese,(3)Productformula,(4)Brieflydescriptionandschematicsaboutthemanufacturingprocesses,(5)Requirementsinqualitycontroltoensurethesafetyoftheproduct,(6)Originalpackagingoftheproduct(includingthedirectionandthelable).IncaseoftheproductwithaproprietarypackagingformarketinginChina,theintendedpackagingdesign(includingthedirectionandthelable)shouldbeprovidedsimultaneously.(7)ThecertificateofanalysisandrelevantdossiersissuedbytheinspectionagencywhichmustberecognizedandacceptedbySFDA,orthecertificateofanalysisonSPF,PFAorPAvalueissuedbyabroadlaboratory,(8)Safetyevaluationdateonmaterialsthatmaybeexistinthefinishedproductswhichhavethesafetyrisk.(9)Applicationforproductsusedinnurturinghair,bodybuildingandbreast,theeffectiveconstituentandthereferenceliteraturescontainingthescientificproofsshouldbeprovide,(10)TheletterofauthorityfortheapplicantinChina(copy),whichhasbeenrecordedbySFDA,andthebusinesslicenceoftheapplicantinChina(copywithofficialseal),(11)Theletterofcommitmentthattherawmaterialandthesourceoftherawmaterialinproductionshouldmeettherequirementsoftherestrictionsorprohibitionsinusinghighriskmaterialsfrombovinespongiformencephalopathy(BSE)diseaseareas,(12)Thecertificateofmanufacturingandmarketingfromthecountry(region)whichtheproductsaremanufacturedorthecountry(region)oforigin,(13)Additionaldossierswhichareconducivefortheadministrativelicensing.1unopenedsampleproductfromthemarketwhichissealedbytheinspectionagencywithlicenseshouldbeprovidedsimultaneously.ThedetaileddescriptionabouttheapplicationdossiersaresetforthinAppendix1.PARTTHREE:Administrativelicensingofimportedcosmeticfornon-particularpurposeAdministrativelicensingofimportedcosmeticfornon-particularpurposeforthefirsttime,theapplicationdossiersshouldbeprovidedasfollows,(1)Applicationformofadministrativelicensingofimportedcosmeticfornon-particularpurpose,(2)ThereasonfornameoftheimportedproductsinChinese,(3)Productformula,(4)Requirementsinqualitycontroltoensurethesafetyoftheproduct,(5)Originalpackagingoftheproduct(includingthedirectionandthelable).IncaseoftheproductwithaproprietarypackagingformarketinginChina,theintendedpackagingdesign(includingthedirectionandthelable)shouldbeprovidedsimultaneously.(6)ThecertificateofanalysisandrelevantdossiersissuedbytheinspectionagencywhichmustberecognizedandacceptedbySFDA,(7)Safetyevaluationdateonmaterialsthatmaybeexistinthefinishedproductswhichhavethesafetyrisk,(8)TheletterofauthorityfortheapplicantinChina(copy),whichhasbeenrecordedbySFDA,andthebusinesslicenceoftheapplicantinChina(copywithofficialseal),(9)Theletterofcommitmentthattherawmaterialandthesourceoftherawmaterialinproductionshouldmeettherequirementsoftherestrictionsorprohibitionsinusinghighriskmaterialsfrombovinespongiformencephalopathy(BSE)diseaseareas,(10)Thecertificateofmanufacturingandmarketingfromthecountry(region)whichtheproductsaremanufacturedorthecountry(region)oforigin,(13)Additionaldossierswhichareconducivefortheadministrativelicensing.1unopenedsampleproductfromthemarketwhichissealedbytheinspectionagencywithlicenseshouldbeprovidedsimultaneously.ThedetaileddescriptionabouttheapplicationdossiersaresetforthinAppendix2.ThecopyoftheletterofauthorityandbusinesslicencearerecordedbySFDAApplicationCenterPARTFOUR:TheprocessflowdiagramofaThecopyoftheletterofauthorityandbusinesslicencearerecordedbySFDAApplicationCenterFilloutaformfromSFDAaFilloutaformfromSFDAadministrativelicensingsystemonlineFormalexaminationFormalexaminationbySFDAApplicationCenter,5wdReviewedbyCHFE,60wdReviewedbyCHFE,60wd（Incaseof（Incaseofdisapprove,theapplicationdossiersareabletoberecoveredbypaperapplicationwithin6months）ApprovApprovedbySFDA,20wdPARTFIVE:ChargeThereisnochargeinadministrativelicensingofimportedcosmeticbySFDA

Appendix1Thedetaileddescriptionabouttheapplicationdossiersforadministrativelicensingofimportedcosmeticforparticularpurpose1.Thedossiersshouldbeprovidedfollowingthelist,2.Fillouttheapplicationformundertheinstructionoftheformnotices,Applicationformforadministrativelicensingshouldbefilledoutbythemanufacturingenterprisesofimportedcosmetic,ortheauthorizerofthemanufacturingenterprises,ortheauthorizedagencyfortheadministrativelicensinginChina.Indicationsshouldbewritteninthesealplaceoftheletterofassurancefrommanufacturingenterprisesincaseofnoofficialseals.LetterofcommitmentinapplicationformshouldbesignedbythelegalpersonoftheauthorizedagencyfortheadministrativelicensinginChina,ortheauthorizerofthelegalperson,withofficialsealontheletter.Whensigninginthepowerofattorney,anotarizedcopyandChinesecopyshouldbeprovided,theconsistentoftheChinesecopywiththeoriginaloneshouldbenotarizedsimultaneously.AccordingtotherequirementsinArticle24of“TheRequirementsOfTheApplicationDossiersForAdministrativeLicensingOfCosmetic”(shortforTheRequirementsOfTheDossiers),theoriginalofthepowerofattorneyandthenotarizedcopyshouldbeprovidedwhiletheapplication,andawrittenexplanationoftheproduct’snameintheoriginalofthepowerofattorney.ThecontentofthesignatureinthepowerofattorneyshouldnotbecontainedbythecontentofthecertificateofauthorizationfromtheapplicantinChina.3.Theproductformulashouldcontaintheconfirmationoftheformulaissuedbytheinspectionagencywithlicense,andthedateoftheconfirmationshouldbeconsistentwiththeapplicationdate.4.Requirementsinqualitycontrolshouldcontaintherequirementsconductedbytheoriginalmanufacturer(foreignlanguageandtheChinesecopy),andaletterofcommitmentdeclaringtheproductsmeettherequirementsin"HygienicStandardforCosmetics".5.Incaseofnoproductdirectionsordirectionsprintedonthecontainers(suchaslipstickandliprougesatcompactsize),therelevantexplanationshouldbemadeinthePackagingPart.6. ThecertificateofanalysisandrelevantdossiersissuedbytheinspectionagencywhichmustberecognizedandacceptedbySFDA,orthecertificateofanalysisonSPF,PFAorPAvalueissuedbyabroadlaboratoryshouldmeettherequirementsasfollows,1)Applicationformforinspection;2)Notificationofacceptanceforinspection;3)Directionoftheproduct;4)Health&Safetytestingreport(microorganism,sanitarychemistryandtoxicology);5)Thedossiersasfollowsshouldbeprovidedincaseofexisting:①Humansafetytestingreport(skinpatchtest,humantrials);②SPF、PFAorPAvaluereports;③Additionalreports(suchasAsbestosinspectionreport).(2)TheapplicationdossierscontainingSPF,PFAorPAvaluereportsissuedbyabroadlaboratory,theadditionaldossiersasfollowsshouldbeprovidedsimultaneously:1)IncaseofthatthelaboratoryhasbeenrecognizedandacceptedbySFDA,theauthenticationcertificateshouldbeprovided;2)Incaseofnoauthenticationcertificate,GCPcertificateorGLPcertificateshouldbeprovided;3)Additionaldossierswhichareconduciveforqualifying.Incaseofthatthereportsissuedbyabroadlaboratoryareprovidedforthefirsttime,theoriginalreport,orthecopywhichisnotarizedbythelocalembassyorrelevantassociationsfromthecountry(region)ofmanufacturer.Thecopyofthereportwouldbeallowedinthere-applicationafterhavingbeenrecognizedandacceptedbySFDA.Theoriginalreportissuedbyabroadlaboratoryshouldbeprovided.Theoriginalreportofatleastoneproductshouldbeprovidedincaseofseriesproducts,thecopyonesofotherproductsareallowed,andtheproductnameintheoriginalreportshouldbepointed.Thecertificateoftherelationshipbetweentheinspectingsampleandthereportissuedbytherelevantlaboratoryshouldbeprovided,whilethereportofabroadlaboratoryisprovidedintheapplicationdossiers.Incaseofthattherelationshipbetweentheinspectingsampleandthereporthasbeenclearlystatedinthereport(suchastheproductnamehasbeennotedinthereport,andthenameofthesampleisconsistentwiththeproductname),thecertificateofaboveisneedless.7.Thecertificateofmanufacturingandmarketingfromthecountry(region)whichtheproductsaremanufacturedorthecountry(region)oforiginshouldmeettherequirementsasfollows,(1)Thecertificateshouldbeissuedbytheregulatoryauthoritiesorrelevantassociations.Thecopyofthecertificateisallowedincaseofwithouttheoriginallone.Thecopyofthecertificateshouldbenotarizedbylocalembassyortheregulatoryauthorities.(2)Thecertificateshouldcontainthenameofproduct,nameofmanufacturer,nameoftheregulatoryauthoritywhichissuesthecertificate,andtheofficialsealorthesignatureoflegalperson(orauthorizer)shouldbeonthecertificate.(3)Thenameofproductandmanufacturershouldbeconsistentwiththeapplicationdossiers.Incaseofcontractmanufacturingorotherwaysandthatthenameofmanufacturerincertificateisn’tconsistentwithapplicationdossiers,awrittenexplanationfromtheapplicantshouldbeprovided.Thecertificateofmanufacturingandmarketingfortheimportedpartoftheproductwhichcontainingvariousformsshouldbeprovided.(4)ThecertificateofmanufacturingandmarketingshouldbetranslatedintoChineseincaseofbeingforeignlanguages.AndtheChinesecopyshouldbenotarizedbynotarypublicinChina.8.Theproductbelongstothefollowingsituations,additionaldossiersasfollowsshouldbeprovidedsimultaneously:(1)Incaseofcontractmanufacturing,additionaldossiersareasfollows,1)Theprotocolaboutcontractmanufacturingbetweentheconsignorandtheconsignee,2)Forimportedproducts,thecertificateofQMSorGMPfromtheconsignee,ortheapprovedcertificateofcosmeticmanufacturingfromthecountry(region)ofmanufacturer,3)Theapprovedcertificateofcosmeticmanufacturingfromthecountry(region)ofmanufacturershouldmeettherequirementsasfollows,①Thecertificateshouldbeissuedbyregulatoryauthorityorthirdparties,Thecopyofthecertificateisallowedincaseofwithouttheoriginallone.Thecopyofthecertificateshouldbenotarizedbylocalembassyornotarypublic.②Thenameandaddressofthemanufactureshouldbeconsistentwiththeapplicationdossiers.(2)Incaseofthemanufacture(applicant)andtheactualmanufacturebelongtoasamecompanygroup,thecertificateoftherelationshipandthequalityassurancedocumentsissuedbythecompanygroupshouldbeprovided.9.Incaseoftheproductismanufacturedbymorethanoneenterprises,oneofthemanufacturersshouldprovidetheaboveapplicationdossiersandadditionaldossiersasfollows,(1)Incaseofcontractmanufacturing,theprotocolaboutcontractmanufacturingshouldbeprovided.Forimportedproducts,thecertificateofQMSorGMPfromtheconsigneeortheapprovedcertificateofcosmeticmanufacturingfromthecountry(region)ofmanufacturershouldbeprovided.(2)Incaseofthemanufacturersbelongtoasamecompanygroup,thecertificateoftherelationshipandthequalityassurancedocumentsissuedbythecompanygroupshouldbeprovided.(3)Theoriginalpackagingfromotheractualmanufactures(4)Health&Safetyinspectionreport(microorganism,sanitarychemistry)fromotheractualmanufactures(5)Theletterofcommitmentthattherawmaterialandthesourceoftherawmaterialinproductionshouldmeettherequirementsoftherestrictionsorprohibitionsinusinghighriskmaterialsfrombovinespongiformencephalopathy(BSE)diseaseareasfromotheractualmanufactures.10.Incaseoftheproductcontainingtheformsofpackagingasfollows,theapplicationsshouldbemadeasthefollowingregulations,(1)Onesamplepackagingcontainsmorethantwo(includingtwo)individuallypackaging,orseparatedsamples(suchaseyeshadow,pressedpowder,blush,etc.),andtheapplicationismadewithoneproductname,thecertificatesofanalysisandformulasofeachseparatedproductsshouldbeprovided.Samplewithoutindividuallypackagingandseparatedsamples,formulasofeachpartsandonecertificateofanalysisshouldbeprovided.(2)TheSamplewithacollectivepackagingwhichcouldnotbesplit,theapplicationismadewithoneproductname,andthesamplehasvariedrawmaterials&statesofmatter,thecertificatesofanalysisandformulasforeachproductshouldbeprovidedrespectively.(3)Incaseoftheproductwhichcontainmorethantwo(includingtwo)formulations,andmustbeusedasamixture,theapplicationshouldbemadeforoneproduct.Accordingtowhethertheproductwithmultipleformulationsisusedasamixtureorseparatedones,thecertificatesofanalysisforthemixtureoreachformulationshouldbeprovided.(4)Incaseofthattheapplicationofimportedproductsaremadebythesamemanufacturingenterprises,whichcontainmorethantwo(includingtwo)originalpackagingwiththesameforeignlanguagenamebutdifferentappearances,thedescriptionoftheappearancesshouldbeaddedtotheforeignlanguagenamecolumnofthecertificateofmanufacturing&marketingandapplicationform,whileattachedwithrelevantexplanation.11.Incaseofthatthesunscreencosmeticswithmultipleserieshaveasamebasicformula,andmakesamplinginspectionfortestingSPF,PFA,PAvalue,theapplicationisallowedtobemadeasonegroupofproduct.Theapplicationdossiersforeachseriesshouldbeattachedwiththenameofeachproductinthisseries,basicformula,colorantslistandsamplinginspectionlist.12.Incaseofthattheimportedproductswhicharemanufacturedbytheenterpriseabroadwithacontractmanufacturingfromresidententerprise,theproductsareprovideashomemadeones.

Appendix2Thedetaileddescriptionabouttheapplicationdossiersforadministrativelicensingofimportedcosmeticfornon-particularpurpose1.Thedossiersshouldbeprovidedfollowingthelist,2.Fillouttheapplicationformundertheinstructionoftheformnotices,Applicationformforadministrativelicensingshouldbefilledoutbythemanufacturingenterprisesofimportedcosmetic,ortheauthorizerofthemanufacturingenterprises,ortheauthorizedagencyfortheadministrativelicensinginChina.Indicationsshouldbewritteninthesealplaceoftheletterofassurancefrommanufacturingenterprisesincaseofnoofficialseals.LetterofcommitmentinapplicationformshouldbesignedbythelegalpersonoftheauthorizedagencyfortheadministrativelicensinginChina,ortheauthorizerofthelegalperson,withofficialsealontheletter.Whensigninginthepowerofattorney,anotarizedcopyandChinesecopyshouldbeprovided,theconsistentoftheChinesecopywiththeoriginaloneshouldbenotarizedsimultaneously.AccordingtotherequirementsinArticle24of“TheRequirementsOfTheApplicationDossiersForAdministrativeLicensingOfCosmetic”(shortforTheRequirementsOfTheDossiers),theoriginalofthepowerofattorneyandthenotarizedcopyshouldbeprovidedwhiletheapplication,andawrittenexplanationoftheproduct’snameintheoriginalofthepowerofattorney.ThecontentofthesignatureinthepowerofattorneyshouldnotbecontainedbythecontentofthecertificateofauthorizationfromtheapplicantinChina.3.Theproductformulashouldcontaintheconfirmationoftheformulaissuedbytheinspectionagencywithlicense,andthedateoftheconfirmationshouldbeconsistentwiththeapplicationdate.4.Requirementsinqualitycontrolshouldcontaintherequirementsconductedbytheoriginalmanufacturer(foreignlanguageandtheChinesecopy),andaletterofcommitmentdeclaringtheproductsmeettherequirementsin"HygienicStandardforCosmetics".5.Incaseofnoproductdirectionsordirectionsprintedonthecontainers(suchaslipstickandliprougesatcompactsize),therelevantexplanationshouldbemadeinthepackagingpart.6. ThecertificateofanalysisandrelevantdossiersissuedbytheinspectionagencywhichmustberecognizedandacceptedbySFDAshouldmeettherequirementsasfollows,1)Applicationformforinspection;2)Notificationofacceptanceforinspection;3)Directionoftheproduct;4)Health&Safetytestingreport(microorganism,sanitarychemistryandtoxicology);5)Thedossiersasfollowsshouldbeprovidedincaseofexisting:①Humansafetytestingreport(skinpatchtest,humantrials);②Additionalreports(suchasAsbestosinspectionreport).7.Thecertificateofmanufacturingandmarketingfromthecountry(region)whichtheproductsaremanufacturedorthecountry(region)oforiginshouldmeettherequirementsasfollows,(1)Thecertificateshouldbeissuedbytheregulatoryauthoritiesorrelevantassociations.Thecopyofthecertificateisallowedincaseofwithouttheoriginallone.Thecopyofthecertificateshouldbenotarizedbylocalembassyortheregulatoryauthorities.(2)Thecertificateshouldcontainthenameofproduct,nameofmanufacturer,nameoftheregulatoryauthoritywhichissuesthecertificate,andtheofficialsealorthesignatureoflegalperson(orauthorizer)shouldbeonthecertificate.(3)Thenameofproductandmanufacturershouldbeconsistentwiththeapplicationdossiers.Incaseofcontractmanufacturingorotherwaysandthatthenameofmanufacturerincertificateisn’tconsistentwithapplicationdossiers,awrittenexplanationfromtheapplicantshouldbeprovided.Thecertificateofmanufacturingandmarketingfortheimportedpartoftheproductwhichcontainingvariousformsshouldbeprovided.(4)ThecertificateofmanufacturingandmarketingshouldbetranslatedintoChineseincaseofbeingforeignlanguages.AndtheChinesecopyshouldbenotarizedbynotarypublicinChina.8.Theproductbelongstothefollowingsituations,additionaldossiersasfollowsshouldbeprovidedsimultaneously:(1)Incaseofcontractmanufacturing,additionaldossiersareasfollows,1)Theprotocolaboutcontractmanufacturingbetweentheconsignorandtheconsignee,2)Forimportedproducts,thecertificateofQMSorGMPfromtheconsignee,ortheapprovedcertificateofcosmeticmanufacturingfromthecountry(region)ofmanufacturer,3)Incaseofthattheimportedproductsaremanufacturedbytheenterpriseabroadwithacontractmanufacturingfromresidententerprise,thepowerofattorney,certificatesofmanufacturingandmarketing,andtheoriginalpackagingwouldnotbenecessary,thepackagingdesignshouldbeprovided.4)ThecertificateofQMSorGMPfromtheconsignee,ortheapprovedcertificateofcosmeticmanufacturingfromthecountry(region)ofmanufacturer,shouldmeettherequirementsasfollows,①Thecertificateshouldbeissuedbyregulatoryauthorityorthirdparties,Thecopyofthecertificateisallowedincaseofwithouttheoriginallone.Thecopyofthecertificateshouldbenotarizedbylocalembassyornotarypublic.②Thenameandaddressofthemanufactureshouldbeconsistentwiththeapplicationdossiers.(2)Incaseofthemanufacture(applicant)andtheactualmanufacturebelongtoasamecompanygroup,thecertificateoftherelationshipandthequalityassurancedocumentsissuedbythecompanygroupshouldbeprovided.9.Incaseoftheproductismanufacturedbymorethanoneenterprises,oneofthemanufacturersshouldprovidetheaboveapplicationdossiersandadditionaldossiersasfollows,(1)Incaseofcontractmanufacturing,theprotocolaboutcontractmanufacturingshouldbeprovided.Forimportedproducts,thecertificateofQMSorGMPfromtheconsigneeortheapprovedcertificateofcosmeticmanufacturingfromthecountry(region)ofmanufacturershouldbeprovided.(2)Incaseofthemanufacturersbelongtoasamecompanygroup,thecertificateoftherelationshipandthequalityassurancedocumentsissuedbythecompanygroupshouldbeprovided.(3)Theoriginalpackagingfromotheractualmanufactures(4)Health&Safetyinspectionreport(microorganism,sanitarychemistry)fromotheractualmanufactures(5)Theletterofcommitmentthattherawmaterialandthesourceoftherawmaterialinproductionshouldmeettherequirementsoftherestrictionsorprohibitionsinusinghighriskmaterialsfrombovinespongiformencephalopathy(BSE)diseaseareasfromotheractualmanufactures.10.Incaseoftheproductcontainingtheformsofpackagingasfollows,theapplicationsshouldbemadeasthefollowingregulations,(1)Onesamplepackagingcontainsmorethantwo(includingtwo)individuallypackaging,orseparatedsamples(suchaseyeshadow,pressedpowder,blush,etc.),andtheapplicationismadewithoneproductname,thecertificatesofanalysisandformulasofeachseparatedproductsshouldbeprovided.Samplewithoutindividuallypackagingandseparatedsamples,formulasofeachpartsandonecertificateofanalysisshouldbeprovided.(2)TheSamplewithacollectivepackagingwhichcouldnotbesplit,theapplicationismadewithoneproductname,andthesamplehasvariedrawmaterials&statesofmatter,thecertificatesofanalysisandformulasforeachproductshouldbeprovidedrespectively.(3)Incaseoftheproductwhichcontainmorethantwo(includingtwo)formulations,andmustbeusedasamixture,theapplicationshouldbemadeforoneproduct.Accordingtowhethertheproductwithmultipleformulationsisusedasamixtureorseparatedones,thecertificatesofanalysisforthemixtureoreachformulationshouldbeprovided.(4)Incaseoftheimportedproductsmadeapplicationbythesamemanufacturingenterprises,whichcontainmorethantwo(includingtwo)originalpackagingwiththesameforeignlanguagenamebutdifferentappearances,thedescriptionoftheappearanceshouldbeaddedtotheforeignlanguagenamecolumnofthecertificateofmanufacturing&marketingandapplicationform,whileattachedwithrelevantexplanation.11.Incaseofthatthesunscreencosmeticswithmultipleserieshaveasamebasicformula,andmakesamplinginspectionfortestingSPF,PFA,PAvalue,theapplicationisallowedtobemadeasonegroupofproduct.Theapplicationdossiersforeachseriesshouldbeattachedwiththenameofeachproductinthisseries,basicformula,colorantslistandsamplinginspectionlist.12.Incaseofthatimportedproductsaremanufacturedbytheenterpriseabroadwithacontractmanufacturingfromresidententerprise,theproductsareprovideashomemadeones.

Appendix3Cosmeticsforparticularpurposeclassification1.Cosmeticsfornurturinghair;2.Cosmeticsforhaircolor（permanentortemporary）;3.Cosmeticsfordepilation4.Cosmeticsforbreast,5.Cosmeticsforbodybuilding(includingforlosingweight)6.Cosmeticsfordeodorization7.Cosmeticsfordispelingfreckle,8.Cosmeticsforsunscreen,9.Cosmeticsforpermorstraighthair.

宝贝计划专卖店创业计划书企业名称：__宝贝计划婴儿用品专卖店创业者姓名：_________________________________________日期：__________________________________________通信地址：_________________________________________邮政编码：__________________________________________电话：____________________________________________传真：__________________________________________电子邮件：__________________________________________目录一、项目介绍------------------------------------3二、市场分析------------------------------------3三、成本预算------------------------------------3四、盈利状况------------------------------------4五、市场风险预测----------------------------------4六、人员机构配置----------------------------------5七、市场营销策略----------------------------------5宝贝计划婴儿用品专卖店计划书项目介绍：项目名称：宝贝计划婴儿用品专卖店经营范围：以出租和出售婴幼儿童车、童床、儿童玩具、婴儿日常用品和孕前孕后的孕妇培训为主，兼做婴儿游泳馆和家政服务信息等。项目投资：10—14万元回收成本期限：15个月（预计）样板店地址：桂林市兴安县（具体地址待定）项目概况：先组建宝贝计划婴儿用品总店，在此基础上，创办一个以片为依托的婴儿用品连锁店。企业宗旨：一切为了宝贝计划。二、市场分析：(一)市场需求分析：1、玩具是孩子的天使，孩子是父母的心肝宝贝。父母对自己孩子的投入是心甘情愿的，但由于各种原因，又不能完全满足孩子对玩具的占有欲望。同时，由于孩子的天性，对玩具喜新厌旧，一个几百元的玩具玩几天就不感兴趣了。而市场上层出不穷的高价玩具，都是孩子永不满足的需求，这样促使了儿童玩具出租行业的萌芽和发展。比如婴幼儿大都需要童车，低档童车价格大约在60—100元，中档童车价格大约在150～300元之间，高档一点的在500元以上，而一部质量较好的童车起码可以用三五年，家庭购买的童车平均使用期为一年左右，不买童车不行，买吧，用完后又很难处理，而且又浪费，所以本店的特色是——既可以出租而可以出售的方法。相似的用品不仅仅局限于童车童床，还有学步车等等。如果开一间婴幼儿童童车童床出租出售店，可以给消费一般的家庭带来实惠，生意肯定兴隆。2、孕前孕后培训也是一个新兴的行业，据市场调查，在此之前没有任何商家以店的形式对准爸爸和准妈妈进行。因为现在的准妈妈准爸爸无法科学的照顾自己的孩子和孕妇