瑞安药业产品新斯诺脚本

合集下载

一诺软件使用说明

采购管理选采购入库菜单中的购进记录管理，或直接点窗口上方按钮行的第一个按钮，打开购进记录管理窗口：首先在来货单位中输入供货单位的输入码（单位拼音开头字母，例如:新海制药厂，输入码为：xhzyc，输入时不区分大小写），按回车选定相应的供货单位。

如果输入开头几个字母例如：xhz 回车，也许会出现“新华制药一厂”等相同开头的单位，用上下键选择一个单位，回车确定。

（注：此输入码及单位名称是在供货方资料管理中定义的）。

增加单位:点此按扭可直接在弹出的窗口中新增供货单位，如下图：按回车后接下来选择采购员：然后用上下键选择采购员，也可打输入码回车直接选择。

（注：业务员输入码及姓名是在企业员工资料中定义的）。

增加采购员:点此按扭可直接在弹出的窗口中新增采购员，如下图：在选择供货厂商或采购员时所填输入码有错，或是资料中找不到相应记录时系统会给出提示，填写正确后，并用左右键选择付款方式（现金或欠款入库）后回车，打开下面录入界面。

调单：可用于调取当日购进记录，但只能对“已录入”的入库票进行编辑，其余入库票只允许查看；如下图所示：输入码以及商品的选择:现在在输入码中打上药品输入码（在药品资料中定）或输入码开头部分按回车，打开下面商品选择窗口：在商品列表中选择入库的药品。

商品列表中上部分显示符合您打的输入码开头的所有药品信息。

下部分显示光标所在药品在当前库存中的库号、批号、数量、有效期等，其中红色的表示已经失效的药品，黄色表示即将失效的药品。

用左右光标键在上下两部分之间切换(当前操作的选择列表上有绿色边框），上下光标键用于选择某批号的药品，最后按回车键确定，方便快捷。

选择入库的药品后，接着输入数量、件数（修改件数，数量也会随着件数的变化而变化。

不须修改的直接回车即可）、进价、批号、有效期、库号后回车，一个品种的药品就算开完了，接下来可以再打输入码开下一个品种，直至完毕。

在输入时可用上下键移动光标位置，ESC键可以清除所有内容，重新打输入码。

SOTAX自动样品准备系统说明书

APW & TPWAutomated Sample PreparationCompliant automated preparation of up to 300 samplesContent/Blend Uniformity, Potency, and Related Substances Assays Simplify extraction of difficult ER, CR, and tamper resistant formulations Robust, reproducible, and fit-for-purpose methodsFor Content Uniformity, Blend Uniformity, Potency, and Related Substances AssaySample preparation can be a very general term. When we talk about sample preparations at SOTAX, we’re referring to the volumetric preparations of API, solid/liquid oral dosage forms, creams, and pastes.Why automate? Automated Sample Preparation enhances laboratory productivity by minimizing resource allocation for repetitive tasks such as sample weighing, extraction, filtration, dilution, and transfer to analysis devices. This enables the repurposing of lab staff to mission critical tasks such as data analysis, reporting, and notebook documentation. Automated procedures can also reduce solvent usage and hazardous waste generation while improving analyst safety by minimizing exposure to hazardous reagents and samples.Do you want to streamline your laboratory workflow? Automation facilitates processing labor-intensive sam-ples for a broad spectrum of challenging formulations including tamper-resistant, osmotic pump, modified, ex-tended, and delayed release. With robust focused extrac-tion techniques the samples are consistently prepared across a variety of analysts and laboratories. Each step is gravimetrically confirmed and tracked in a secure data-base to ensure reproducible, high quality, traceable, compliant results.Recent initiatives to incorporate QbD and Continuous Process Improvement principles into the drug product lifecycle management process have increasingly raised laboratory productivity expectations. The demand for more sample throughput with the same or reduced head count is being imposed on laboratories across the industry. With 100’s of installations globally, processing hundreds of thousands of samples, SOTAX Automated Sample Preparation Systems have proven to be reliable and compliant solutions to enhance your laboratory’s effi-ciency and accelerate the workflow.Why Automate Sample Preparations?Automated… and in with the improved!Automate your sample preparationsso that they are performed the sameway every time. Each method stepis confirmed gravimetrically, repor-ted volumetrically, and docu m ent e delec t ronically.You will improve overall lab cycletimes and reduce solvent costs.Manual Out with the old …Volumetric glassware for tablet, capsule, and blend evaluations have long been the industry standard. Unfortunately, so have bottlenecks, OOS investigations, and excessive solvent costs. Traditional sample preparation relies on technique-dependent and labor-intensive laboratory steps often requiring error-prone data transcription.Coupled with the limited extraction efficiency of stirring, shaking, and sonication mechanisms, manual sam p le preparation is at the root of many time-consuming and costlylab investigations.APW and TPWEnhanced for Greater ProductivityThe APW and TPW Automated Sample Preparation Systems have recently been enhanced to provide even greater sample preparation productivity and reduced cycle time while streamlining your laboratory workflow. The TPW and APW provide productivity solutions to a broad variety of laboratories and applications. Typical products range from solid or liquid oral dosage forms for the pharma-ceutical industry to tooth paste and lipstick for the consumer products industry. Regardless of the industry or the degree of regulation, these platforms maximize efficiency and throughput for a vast array of applications. From API to suspen-sions to tablets to medicated feeds, the TPW and APW provide a range of support from simple sample preparation to barcoded sample ID and preparationwith on-line HPLC analysis and compliant data transfer to your validated CDS.> APW and TPWAutomated Sample Preparation WorkstationsExtractionThe TPW uses a high-shear homog-enizer probe to provide a consistent wet grinding process to quickly ex-tract samples. Alternately, the APW has a sonication probe coupled with a UV temperature sensor to deliver focused sample disintegration with-out overheating. With these tools, both TPW and APW can achieve effi-cient and reproducible extraction for even the most challenging of sample formulations. Cleaning of the extrac-tion path between samples is easily programmed into the method to eliminate sample carry-over, ensur-ing that each sample is handled iden-tically. The newly updated TPW and APW are enhanced to reduce cycle time by adding efficiency to the system cleaning process.Filtration & DilutionThe TPW uses a fluid metering pumpto filter extracted samples as theyare transferred from the extractionvessel to test tubes. Both the TPWand the APW also support a syringe-driven filtration process to filter so-lutions from one test tube to another.Post filtration, both systems can per-form up to 1:100,000 dilutions withina single method. Further dilutionsare also possible using the “MethodOverlap” feature. The volumes for allliquid handling operations are con-firmed gravimetrically for addedaccuracy and precision. For everysample, the system audit trail com-bined with the advanced error han-dling capabilities provides a detailedand comprehensive record of the en-tire preparation process.Analysis & StorageBoth units have HPLC injectors tosupport on-line HPLC analysis. AWaters Empower TM interface is alsoincluded to provide compliant datatransfer to Empower TM for stream-lined sample analysis with enhancedtraceability. All result-critical sam-ple preparation information is trans-ferred to Empower TM as the TPW/APWsample run-list progresses. In addi-tion to on-line HPLC analysis, sam-ples can also be collected in sealedHPLC vials to support various off-line analyses. Finally, both the TPWand APW have the capability to trans-fer sample to a UV spectrophotometerto act as an autosampler for on-lineUV analysis. The systems will thenuse an analog connection to triggerthe UV to read the sample in accor-dance with the external UV instru-ment control program.Fully Automated Steps> SAM Sample ManagerCollect samples with optionalcooling for off-line analysis orfurther processingBenefitsPerform High Quality Preparations Automated Sample Prep means robust and reproducible preparation that is equivalent or superior to your manual analytical procedures. Robust and reproducible means that automation guarantees uniform sample history.Sample weighing capabilities include 4- or 5-place weighing with automatic switching to 4-place mode for gravimetric confirmation of volumetric sample dilutions.“Uniform sample history in automatedsample preparation eliminates bias and error introduced by inconsistencies in manual preparation.”sample preparation method. This can result in Due to the physics of the focused homogenizerReduce and Simplify OOS InvestigationsDeficiencies in laboratory investigations are a major source of warning letters in the pharmaceutical industry, accounting for 12 % – 15 % of 483s annually. With TPW and APW, each method step is gravimetrically confirmed and recorded in the secure database to ensure high quality consistent results. The TPW and APW audit trail provides a compliant and comprehensive history of the entire sample preparation process. In the event of an unexpected result, this audit trail ensures a well-defined assignment of root cause to simplify the laboratory investigation process.“DOE and QbD for analytical methods are no longer just buzz words. TPW and APW are ‘designed for experiments’… today.”Automate Your Method Development Our user-friendly software interface provides rapid assimilation of the TPW and APW platforms in all envi-ronments from academic to industry AR&D to the QC lab. Advanced developer options accelerate the method development process to facilitate Analytical Quality by Design (AQbD). AQbD pairs good scientific principleswith quality risk management. Combined with the Empower™ interface, TPW and APW’s powerful dEsign™ variables fully automate AQbD to ensure robust, fit-for-purpose methods that deliver consistent results throughout the method lifecycle. These powerful soft-ware functions allow you to plan and execute method development DOE activities quickly and efficiently. The easy-to-use and intuitive software interface stream-lines the method transfer across sites.“No more auditing of pipettes and volumetric flasks and no need to store glassware around the lab for weeks.”SpecificationsAPW TPWMax. Sample Throughput per Run 300 samples (extraction mode 1 & 2)100 samples (extraction mode 1)200 samples (extraction mode 2)Sample Containers • 16 × 100 mm tubes• 20 × 150 mm tubes• 16 × 150 mm tubes• 16 × 100 mm tubesSample Confirmation5-place and 4-place weighing(min. weight of 100 mg or 200 mg, respectively)5-place and 4-place weighing(min. weight of 100 mg or 200 mg, respectively)Sample Tracking Linear barcode reader Linear barcode readerExtraction & Liquid HandlingExtraction Mode 1Sonicator (with UV Temperature sensor)Homogenizer (2k RPM – 20k RPM) Extraction Mode 2Vortexer VortexerExtraction Volume• 1 mL – 10 mL (16 x 100 mm test tube)• 20 mL – 100 mL (extraction vessel), or• 50 mL – 520 mL (extraction vessel), or• 1 mL – 10 mL (16 x 100 mm test tube) Filtration Syringe Fluid metering pump and syringe Syringe-driven LiquidDispensing0.05 mL – 10 mL0.05 mL – 10 mLMax. Dilution Ratio1:100,0001:52,000,000Max. Number ofSolvents Connected9 solvents 5 solventsAnalytical FinishOff-Line• Sample collection in test tube rackson APW platform• Sample collection into sealed vials in SAM • Sample collection in test tube racks on TPW platform• Sample collection into sealed vials in SAMHPLC On-Line• HPLC fixed loop injector• incl. Waters Empower TM interface • HPLC fixed loop injector• incl. Waters Empower TM interfaceUV-Vis On-Line Sample collection followed by automated transferinto UV-Vis Sample collection followed by automated transfer into UV-VisControls (Minimum Requirements)PC• Windows 7-64 bit • Dual Core ProcessorDatabase• MS SLQ Server 2000 or greater • Express, Workgroup or Standard EditionDimensionsAPW / TPW AutomatedSample Prep. Workstations• Height: 42” / 107 cm (incl. Light Tower) • Width: 45.5” / 116 cm (with balance LCD panel) • Depth: 36” / 91 cm SAM Sample Manager• Height: 27.5” / 69 cm • Width: 21.5” / 55 cm • Depth: 30” / 76 cmTechnical ServicesGlobal. Reliable. Customer-focused. The SOTAX Global Service Network is available worldwide, whenever and wherever you need us.• System installation and qualification• User training• First Line Responder training• Preventive maintenance• Technical support• Repairs• Updates, upgrades, and customization• Compliance services (cGMP compliant qualification: IQ, OQ, PQ, and customer-specific qualification)• Service contracts• RelocationsAssociated ServicesApplication ServicesAt SOTAX, we engineer solutions for development and quality control.We support you with expertise at each step of your process:Feasibility study Secure your instrument investment with data confirmation of “fit forpurpose” method capability on your productsMethod development Save time and resources by allowing SOTAX application scientists todevelop your methods in accordance with your method developmentrequirementsMethod transfer Use our trained hands to provide method training and facilitate thetransfer of your automated methods across sitesMethod validation Speed rollout by allowing us to facilitate and document validation ofyour method at your siteApplication support at installation Screen your applications for potential hurdles and prioritize methods to be automated to develop an efficient and effective plan for integrating automation into your laboratoryApplication training Come to our labs or invite SOTAX into yours to work with ourapplication experts to streamline the automation of your methods 11SOTAX > Automated Sample Preparation > APW & TPWEuropeSwitzerland (HQ Europe)Aesch/BaselP Tech Support +41 61 487 5460P Offi ce +41 61 487 5454info @Czech Republic PragueP Tech Support +41 61 487 5460P Offi ce +420 246 039 260info @France Saint-LouisP Tech Support +41 61 487 5460P Offi ce +33 3 8970 0846info @Germany LörrachP Tech Support +41 61 487 5460P Offi ce +49 7621 16 5635info @Great Britain LondonP Tech Support +44 20 8349 6946P Offi ce +44 20 8349 6947info @Italy MilanP Tech Support +41 61 487 5460P Offi ce +39 02 8363 2641sotaxitalia @AmericasUSA (HQ Americas)Westborough, MAP Tech Support +1 508 544 4040P Offi ce +1 508 417 1112sotaxusa @Canada BramptonP Tech Support +1 800 931 4151P Offi ce +1 905 494 0114sotaxcanada @Asia-PacificIndia (HQ Asia-Pacifi c)MumbaiP Tech Support +41 61 487 5460P Offi ce +91 22 42 95 01 -91 / -92sotaxindia @China ShanghaiP Tech Support +41 61 487 5460P Offi ce + 8621-6135 6268, ext. 205sotaxchina @SOTAX WorldwideM B 30002E N _02_2015-11。

Intouch函数脚本与逻辑使用指南

商标
本文所提及且已知为商标或服务标志的所有专用名词均已采用适当的首字母大写形式。 Invensys Systems, Inc. 无法证实此类信息的准确性。在本文档中使用某个专用名词不应视为会影响任何商标或服务标志的有效性。 Alarm Logger、 ActiveFactory、 ArchestrA、 Avantis、 DBDump、 DBLoad、 DT Analyst、 FactoryFocus、 FactoryOffice、 FactorySuite、 FactorySuite A2、 InBrialRAD、 IndustrialSQL Server、 InTouch、 MaintenanceSuite、 MuniSuite、 QI Analyst、 SCADAlarm、 SCADASuite、 SuiteLink、 SuiteVoyager、 WindowMaker、 WindowViewer、 Wonderware 以及 Wonderware Logger 均为 Invensys plc 及其子公司与附属公司的商标。所有其它品牌可能是其相应所有者的商标。
$LogicRunning 系统标记 ................................................37
第 4 章脚本语言 ................................................39
基本语法规则 ......................................................................40 子程序 ..............................................................................40 语句.................................................................................. 40 缩进.................................................................................. 40 注释.................................................................................. 40 标记引用 ..........................................................................41 数据值 ..............................................................................41 值表达式 ..........................................................................41 语法验证 ..........................................................................41

(演讲版)瑞安药业核心产品新斯诺左炔诺孕酮滴丸产品讲义

4、药物在基质中分散均匀，单剂量更加准确； 5、滴丸剂与片剂，胶丸等其他制剂相比，最显著的特点在于作用迅速，生物利用度高，可保障药物合理的使用剂量。
新斯诺生物等效试验
100%安全100%有效新斯诺
片剂曲线分布比较分散血药浓度范围为8-29ng/ml
滴丸曲线分布比较集中血药浓度范围10-18ng/ml
质量控制
u
气流粉碎粒子撞击原理示意图 Page 20
三. 新斯诺产品特点和价值
100%安全100%有效新斯诺
Page 21
新斯诺产品介绍
优质商标
100%安全100%有效新斯诺
国内外20年专利唯一滴丸类紧急避孕药
商标名：新斯诺
性状：白色至淡黄色滴丸。剂型：滴丸规格：0.75mg×2粒/盒临床适应症及用法用量：
崩解特点药物内左炔诺孕酮含量均匀，入口即开始吸收，不会出现呕吐，绝对（安全性）安全
有效率据最新临床研究证明新斯诺有效率据不完全统计有6%的消费者出现避孕失败高达 99.9% ，为行业内最高（有效性）
服用时间很方便：72小时内随时服用，随买麻烦：需要在饭后或睡前吃，以减少呕吐的发随服，可以空腹服，可以饭后服，生，对紧急避孕起限制时间作用，不方便（方便性）可舌下含服达到血药峰平均2小时，不呕吐，不影响避孕效果值时间专利保护
左炔诺孕酮滴丸获得国临床批件
Page 19
新斯诺优势比较
标准
原料辅料
100%安全100%有效新斯诺
左炔诺孕酮滴丸
通过气流微粉化到小于1微米粒径细粉（特点：粒径细不产热）
左炔诺孕酮片（胶囊）
通过机械粉碎粒径多在50微米以上（粒径粗、易产热）国产淀粉、微晶纤维素等片剂填充辅料

智能药片测试系统 SmartTest 50说明书

Swiss QualityHigh quality components paired with Swiss preci-sion engineering provide for a long product life and minimize costly machine downtime. In order to ensure maximum reliability of your SmartTest 50, all instruments are tested according to strict inter-nal quality standards before they leave our factory. Hardness TestingW ith more than 40 years of experience and more than 20'000 testers in the market, Dr. Schleuniger ® Pharmatron measuring technology is a safe invest-ment. Like all our hardness testers, the SmartTest 50 offers consistently accurate test results and fully complies with current USP (chapter 1217, tablet breaking force) and EP (2.9.8, resistance to crushing of tablets) requirements.Quality matters.C er t if i e d S y s t e mI S O9001SmartTest 50The SmartTest 50 sets new standards in fast and efficient semi-automatictesting of up to five physical parameters. Weight, thickness, width, diameter/length and hardness of virtually all tablet shapes can be tested in full compli-ance with current Pharmacopeia requirements. Proven Dr. Schleuniger®hardness measuring technology guarantees accurate and highly reliable testdata that can be evaluated immediately. An integrated color touch screen withsimple icon-based navigation makes operating the SmartTest 50 very intuitive consequently reducing operator training time to an absolute minimum. Per-fectly suited for both laboratory and production environments, the SmartTest50 has been designed to optimize efficiency of your quality control processwithout limiting the range of possible applications.→ SmartTest 50Semi-automatic tablet testing system→ Semi-automatic testing of virtually all tablet shapes and sizes with the SmartTest 50→ SmartAlign TM to measurediameter & hardness→ SmartAlign TM to measure width → SmartAlign TM to measurelength & hardnessThe SmartTest 50 is capable of testing virtually all tablet shapes and can easily be programmed to meet your individual testing requirements. Tablet samples are placed in a feeder carousel by the operator and all further testing is done automatically. The patented SmartAlign TMsystem guarantees reliable orientation of samples in the integrated measuring stations and automatically turns both oblong and oval shapes for width and length measuring prior to hardness testing.Smart, Smarter, SmartTest 50Especially when it comes to testing oval, oblong or other shapes, the SmartTest 50 combines maximum flexibility with reliable tablet orientation for high precision results. The integrated single-flap SmartAlign TM system ensures correct positioning of test samples at all times. As a standard, the SmartTest 50 first measures the width of tablets and then quickly re-positions them for precise length and hardness measuring – all in the same integra-ted measuring station. If width measuring is not required, tablets are immediately oriented for combined diameter (length) and hardness measurement.After each measurement, an integrated cleaning function removes debris and broken tablet fragments from all contact surfaces of the hardness station for trouble-free operation. Short cycle times are maintained at all times.To «future-proof» your investment, the SmartAlign TM system does not limit the application range of the SmartTest 50 in any way. From small to large tablet sizes – almost all shapes can be tested in standard configuration. When equipped with a custom feeder carousel, there are no limits for testing even the most complex specialtablet shapes.BCAAccommodating for most standard testing needs, up to 23 tablet samples are measured in one test run. If testing larger sample sizes is required, results from several test runs can be combined in a single test report – with the push of a button.Only the combination of quality components, state-of-the-art electronics and correct tablet orientation provides test results you can rely on. The SmartTest 50 with pro-ven Dr. Schleuniger ® Pharmatron measuring technology complies with all current USP and EP requirements and offers consistently accurate results. Tablet hardness is measured using a precision S-beam load cell with a line-arity of 99.95% over the entire measuring range. Featuring innovative light-weight construction, the integrated thickness gauge is extremely precise and applies only minimal pressure on tested tablets. To ensure stable test conditions – particularly for the integrated balance – the SmartTest 50 can be equipped with an anti-static safety cover protecting all measuring stations.Flexibility and Precision→ Top view of SmartTest 50 A: Integrated balance (depending on model) B: Thickness measuring stationC: Width / Length (Diameter) / Hardness measuring stationwith integrated SmartAlign TM system6Hardness testing → Semi-automatic tablet testing system →SmartTest 50→ Fast and intuitive icon-basedtouch screen operationOperating a semi-automatic tablet testing system has never been easier. The intuitive icon-based touch screen user in-terface sets new standards for fast and user-friendly control. Three test modes allow using the SmartTest 50 according to individual reporting requirements.From executing simple tests to programming products with T1/T2/PL limits and methods – everything is configurable using the touch screen menu. Intuitive icon-based navigation and logical menu structures with intelligent operator assistance provide for fast test setup, short training time and error-free data entry.Different views can be selected while test runs are executed, allowing theoperator to display currently measured value, complete series of measure-ments and even graphical hardness curves. Professional reports are auto-matically printed at completion of a test run.For paperless reporting and central data management in full compliance with 21 CFR, Part 11 requirements, the SmartTest 50 can be networked with the q-doc PC er-friendliness“FullTest” modeAll product and method specifica-tions can be pre-programmed and easily retrieved for fast test setup. Up to 100 products including nominal values and T1/T2/PL limits for all test parameters are conveniently stored directly on the SmartTest 50. Oncompletion of each test run, a com-prehensive report is printed automa-tically. The report shows all product and test parameters, calibration data and individually measured valuesalong with statistical analysis.“EasyTest” modeFor tests without T1/T2/PL limits, the “EasyTest” mode allows fast anduncomplicated setting of the desiredsample size for each parameter. No programming of product specifica-tions is required. The same reportingfunctions as in the “FullTest” mode are available.“SingleTest” modeTo quickly measure single tablets without printing a report, simply ac-tivate the parameter(s) you would like to test and press start.PC SoftwareAll SmartTest 50 tablet testers can be connected with PC software for 21 CFR, Part 11 compliant electronic data management. M easured results and test reports are collected in a data-base and can be exported in various formats such as PDF, XM L, HTM L, and TXT.→ Example: q-doc with 2 x SmartTest 50(TDH version and WTDH version)→ TDH version, connected to external balanceThe SmartTest 50 with external balance inter-face (instead of being equipped with an inte-grated weighing module) has been designed for alternative testing requirements.The operator first measures the weight of samples individually on a connected external balance and then places them in the SmartTest 50 feeder carousel. Measured results are automatically transferred to the tester. As soon as the required sample size has been reached, testing of thickness, width, diameter/length and hardness parameters proceeds automatically. Upon completion of the test, a report with all results – including manually measured weight values – is auto-matically generated.Models20014042016-01Your local sales & service partner1。

Foregene RT EasyTM I 说明书

RT Easy TM IMaster Premix for first-strand cDNA synthesisCat.No.RT-01011/01012Fast and highly sensitive reverse transcription system for generating first-strand cDNA using pg-level RNAFor research use only Store at-20℃目录产品介绍 (3)产品特点 (3)试剂盒应用 (3)产品质量控制 (4)试剂盒内容 (4)运输及储存条件 (4)试剂盒组分信息 (5)注意事项 (5)RT Mix耐受性 (6)●酒精耐受性分析 (6)●胍盐耐受性分析 (6)操作前准备事项 (7)逆转录引物用量 (7)RNA模板用量 (7)实验材料和设备 (7)自备试剂 (8)安全性 (8)操作指南 (9)操作示意图 (10)问题分析指南 (11)本公司的2×RT Easy TM Mix合成第一链cDNA的温度高达50℃，有利于复杂二级结构RNA模板进行逆转录反应。

实验室纯化获得的RNA常有酒精及胍盐残留，对大多数逆转录酶有很强的抑制性，导致逆转录效果不理想或逆转录效率低。

福际2×RT Easy TM Mix对酒精和胍盐显示出极高的耐受性，对RNA样品中酒精的最高耐受为45%，胍盐的最高耐受为750mM。

即使不纯的RNA也可用福际2×RT Mix进行逆转录反应。

独特的反应体系,使得RT反应更加简便、快捷、高效，25min即可完成第一链cDNA的合成。

此产品可与Foregene公司的荧光定量产品Real Time PCR Easy TM配合使用，能获得高质量的实验结果。

产品特点◆高效的逆转录体系，只需25min即可完成第一链cDNA的合成。

◆高灵敏的逆转录体系，pg级别的模板也可以得到高质量的cDNA。

S2 Pharma Laser 产品说明书

C h e c k w e i g h e r sLaser marker operating terminalOption: combined use of a single operating terminal for all data entries etc.(operation of the laser marker is through the weighing terminal)GARVENSS2 Pharma Laser• dynamic checkweighing and industrial laser marking • in one perfect operation• with Garvens checkweigher S2, Sator laser marker and OCR cameraRenowned specialists have combined to offer a system of the highest quality made in Germany:GARVENS checkweighers of the S2 design series are the result of focused research and development, with their proven technology they are used world-wide. Sator Laser – a leading company in industrial laser marking technology – now offers the optimum enhancement to the S2 checkweigher: the DynaMark ®laser,top performer wherever the transfer of information onto a package surface is required, whatever the packaging material.New cost-saving process with low laser power: white pharmaceutical cartons can now be printed with dark lettering in highest quality (prerequisite is that the surface to be marked is coated with laser-sensitive ink). Monitored by a camera check system using OCR equipment. Process synchronization, enormous cost advantages due to integrated system. The overall system can be validated to 21 CFR part 11.CharacteristicsS2 checkweigher• "Weights and Measures" approved in specified countries (on enquiry)• automatic or manual re-zero control• askew packages detection (prior to laser marking)• open flap detection• flexible integration into production lines• transversal adjustment facility for laser marker and weighframe• follows GMP philosophy• rejection of wrongly printed (laser marked),off weight, unsealed, and wrongly orientated products • total system easy to service – easily accessible Weighing terminal• touch screen, colour LC display: TFT 12.1",resolution 800 x 600 pixel (SVGA)• user-friendly: TachoControl-style gauges, operator prompts/menus• multiple language support for on-screen dialogue • 200 article memory locations• up to 7 weight zones for weight classification • password protection for multiple access levels • networks (Ethernet, FreeWeigh)• comprehensive display of all current, important weight and production data or configuration screensTechnical details SchematicGARVENSS2 Pharma LaserWeighing range*within the range 0 to 600 g, specific to article weight Accuracy** from ±0.02 gThroughput (weighings / minute)** max. 250Roller centres (A-A), weighing conveyor 200, 250 mmBelt width (B-B), weighing conveyor100, 120, 150, 200 mm Roller centres (A-A), infeed/outfeed conveyor 250, 400, 600, 800 mm Belt width (B-B), infeed/outfeed conveyor100, 120, 150, 200 mm Standard sorting/rejecting deviceair jet* depending on the design and dimensions of the weighing belt used** depending on the weight, dimensions and transport behaviour of the product to be weighedTypical dimensions in mmSubject to technical modifications.Printed in Germany 0605/98 UK© Mettler-Toledo Garvens GmbH Kampstrasse 7D-31180 GiesenTelephone +49 (0) 5121 933-0Facsimile +49 (0) 5121 933-456********************Visit us atSator Laser 'T Series' laser marking unit • vector marking technology for superb, clear quality of texts, logos, special characters and graphics• unequalled speed of operation • maximum reliability and uptime • minimum maintenance• high positioning and repeat accuracy due to DynaMark ®laser printing software• absolute safety due to countercheck and OCR camera system (optical character recognition)• extraction systems with functional and exhaust air monitoring。

药厂urs编写范本 -回复

药厂urs编写范本-回复药厂URS编写范本：药物研发与生产工艺一、引言药厂URS（用户需求规范）是制药行业中一份关键的文档，它详细描述了药厂所期望的药物研发与生产工艺的需求。

本文将一步一步回答关于药物研发与生产工艺的URS编写范本。

二、背景在这一部分，需要对药厂进行简短的介绍，并阐明背后的动机。

例如，该药厂的历史背景、经营理念和市场定位等。

三、目标这一部分需要明确药厂药物研发与生产工艺的目标。

例如，提高生产效率、降低成本、优化质量控制等。

四、药物研发与生产工艺1. 药物研发a. 新药研发流程：详细描述药物研发的各个阶段，包括药物发现、药物设计、药物合成等。

b. 药物研发技术要求：列出所需要的技术设备、实验室设施、研发团队等要求。

c. 研发项目管理：说明项目管理的方法和流程，包括进度控制、质量管理和风险评估等。

2. 药物生产工艺a. 生产流程：详细说明药物生产的各个阶段，如原料采购、制剂生产、包装等。

b. 生产设备与工艺控制：列出所需的生产设备和工艺控制要求，包括技术参数和操作规范。

c. 质量控制：阐明所需的质量控制系统和相关要求，包括质量检测和数据记录等。

d. 安全与环境保护：说明对于员工安全和环境保护的要求，包括安全培训和应急预案等。

五、验收标准这一部分需要确立药物研发与生产工艺的验收标准。

例如，药物研发成功的判定标准、工艺设备验收标准、药物质量合格标准等。

六、项目时间表与预算在这一部分，需要列出项目的时间表和预算。

明确项目的开始和结束时间，以及整体预算和分期付款计划等。

七、附件将所有的附件清单列出，这些附件可能包括技术文件、生产数据、市场调研报告等。

八、结论总结药物研发与生产工艺URS的编写内容，强调药厂的期望和需求。

同时，提醒读者核对URS编写的准确性和完整性。

九、致谢感谢相关人员对于药物研发与生产工艺URS编写工作的支持与帮助。

通过以上的URS编写范本，药厂可以详细阐明药物研发与生产工艺的需求，以便与设备供应商和合作伙伴进行有效的沟通和合作。

Eyecon 药房自动化系统说明书

Prescription Validation,Counting and Filling SystemRevolutionary Tabletop AutomationDistributedBy:*******************************Eyecon® is a revolutionary pharmacy automation system Eyecon is fast becoming the preferredchoice of pharmacies that have decidedto automate their prescription fillingprocess. Filling automation improves Rxaccuracy, resulting in improved customersafety, inventory control and customersatisfaction, saving an average pharmacythousands of dollars per year.Eyecon’s unique Visual Counting System™is up to 76% faster and significantlymore accurate than manual counting.It helps reduce tedium and stress whileallowing employees to spend more timewith customers. Customers benefit fromimproved customer service andRx accuracy.How Eyecon worksThe Eyecon is a unique machine visioncounting system. A camera mounted above the counting platter captures photo images used to count pills five times per second. An added benefit of the machine vision technology is thedetection of pill fragments or foreign matter on the counting platter. The Eyecon alerts the operator when pill fragments or foreign matter are present on the counting platter. This feature ensures the quality of the prescriptions filled on the Eyecon.Safety –• Validation mode ensures customer safety with proper dispensing. Separate sulfa and penicillin platters prevent cross-contamination. Speed –• Counts poured pills in 200 ms,updating pill count up to 5 times per second. Accuracy –• Field-tested near 100%.Confidence – • Open design ensures quick and easy visual inspection of medication.Quality – • Recognizes and identifies tablet fragments and foreign material on platter.Versatility – • Counts all sizes and shapes of capsules and tablets. Can also be used for validation and inventory of ointments, creams, solutions and pre-packs. Longevity – • Regular updates to drug database and user interface.Cleaning – • No hidden compartments or disassembly required.The highlighted shadow images represented on the left side of the display illustrate the location of the pill fragments or foreign matter on the counting platter.Operator displayMachine visioncameraCounting trayBarcode readerDispensing spoutSulfa/penicillin platter storage1 425365/2010 eyecon_L_500353.indd (C&D) AWT35-500353© Avery Weigh-Tronix, LLC 2010. All rights reserved. This publication is issued to provide outline information only which, unless agreed by Avery Weigh-Tronix, LLC in writing, may not be regarded as a representation relating to the products or services concerned. Avery Weigh-Tronix, LLC reserves the right to alter without notice the specification, design, price or conditions of supply of any product or service.1000 Armstrong Drive Fairmont, MN 56031-1439*********************Toll-Free: (800) 533-0456 Phone: (507) 238-4461SPECifiCAtionSPlatter Surface Area:• 48” sqDimensions:• 28” H x 11” W x 17.5” D Weight:• 16-18 lb (28 lb ship weight)Screen:• 6.5” Color LCD flat panel touchscreen Integrated Barcode Scanner:• Class I Laser, Standard symbologies Warranty:• One year limited Pill database updates • Interfaces to pharmacy• management software systems Two (2) USB Ports • Ethernet Port• Power:•100-240 VAC, 47-60 HzApprovals:• FCC, ETL US Patent # 7,599,516•performed 5 times to calculate average Rx fill time.Individual results may vary.Pill Count Product Avg. Fill Time 30 pillsGSE Eyecon®13.6 sec GSE Model 664 Scale 15.6Competitive brand 17.1Hand counting 26.960 pillsGSE Eyecon®14.1 sec GSE Model 664 Scale 16.9 Competitive brand 21.9Hand counting 47.790 pillsGSE Eyecon®15.9 sec GSE Model 664 Scale 17.0Competitive brand 26.8Hand counting66.6For more information or to arrange for a free demonstration unit, please visit us at: *********************866-260-6540Your local representative is:T o schedule an in-house demo800-922-9142oremail:*******************。

riboSCRIPTTM mRNA lncRNA qRT-PCR Starter Kit 使用说明说

ribo SCRIPT TM mRNA/lncRNA qRT-PCR Starter Kit使用说明RN：R11088.2产品简介ribo SCRIPT TM mRNA/lncRNA qRT-PCR Starter Kit是研究基因表达变化的通用检测方法。

然而，与mRNA 不同的是，lncRNA 表达水平相对较低，通常需要进行多个要素的系统优化才能准确地检测分析。

ribo SCRIPT TM mRNA/lncRNA qRT-PCR Starter Kit是锐博生物推出的基于SYBR Green I 嵌合荧光法的qRT-PCR 试剂盒，其包含已优化浓度的RT 酶，Taq 酶，缓冲液，SYBR Green I 荧光染料，RT引物和内参qPCR引物，仅需结合推荐浓度的qPCR引物即可实现mRNA或lncRNA表达情况的快速、高效、准确的检测。

运输保存产品需低温运输。

收到产品后，请于-20℃保存，可以稳定保存一年。

使用前须知使用前请瞬时离心，以免制品粘附于管壁或管盖上，造成损失或污染。

血浆/血清/外泌体的mRNA/lncRNA qPCR检测需要在提取RNA前加入外参。

实验方法1. mRNA/lncRNA RT反应1）取Random Primer (200µM) 和Oligo (dT) 18 (25µM)，恢复至室温，振荡混匀。

2以上体系混匀后，瞬时离心，RT反应程序为：42℃60 min，70℃10 min。

注：1）Random Primer和Oligo (dT)混合使用，可以高效合成cDNA。

实验目的不同，也可以用单引物或者基因特异性RT引物，使用量如下：2）RT反应结束后请立即将cDNA产物取出，快速置于冰上冷却备用或-20度以下保存；3）体系可按照实验需求等比放大，20μL反应体系建议不超过5μg的Total RNA。

2. mRNA/lncRNA qPCR反应1）SYBR Green Mix：包括Taq酶、dNTP mix、PCR Buffer、SYBR Green Ⅰ等。

历史上最敢的要价的避孕药

历史上最敢的要价的避孕药-山东瑞安药业售价100元呀，"新斯诺"采用了不同于其他同类成分产品的制剂工艺，它采用先进的"固体熔融分散技术"。

运用该技术生产的"滴丸"剂型是当前该类紧急避孕产品的独家剂型，解决了其他剂型产品所固有的"药物含量很难做到均衡，副作用较大"的痼疾，从而保证了药物分散的均一性，实现了"避孕成功率高，身体损害小"的要求。

山东瑞安药业有限公司成立于1968年，是一家集科研、生产、销售于一体的现代化制药企业。

瑞安人是一批追求卓越的人，为了人类的健康，不惜成本，在各个环节都坚持高标准严要求。

"新斯诺"就是采用当前国际最高标准生产的紧急避孕药，从而保证了该产品的卓越品质。

山东瑞安药业有限公司成立于2002年，是一家集新药研究、开发、生产、销售于一体的创新型医药集团，现有员工总人数400人，资产突破8000万人民币。

瑞安药业旗下三大分公司：新斯诺生物科技有限公司、瑞安医药销售公司及维舒制药（筹建）。

瑞安药业以“成为人类健康产业领导者”为己任，不断学习和运用先进的医药技术，以人类健康需求为出发点，不断研制开发具有市场价值的医药品种，主要涵盖肿瘤、心脑血管、OTC药品、眼科和大健康产品等领域。

其中，抗癌止吐药物盐酸托烷司琼产品销量位列品类第一名；20年专利保护紧急避孕药新斯诺左炔诺孕酮滴丸被誉为“百姓信赖妇科用药”。

瑞安人清楚的知道：产品品质是决定经营成败的基础条件；只有不断创新的企业才有未来。

瑞安药业秉承：“精心制好药健康中国人”的企业愿景，坚持“诚信、创新、共赢、卓越”的企业文化，努力开拓国内市场，力争把企业打造成为中国综合创新型制药领先企业。

公司拥有一支具有行业领先水平的资深研发团队，拥有50多项自主研发的核心技术和知识产权。

未来十年，瑞安药业继续围绕人类健康需求持续创新，全力打造瑞安40亿计划，提供完全值得信赖、更加卓越的产品和服务，做到每一款产品都会使消费者感到满意，给参与者带来经济利益和荣誉感。

新式药物说明书_初三作文范文

新式药物说明书_初三作文范文
一、药品名称
通用名称：XXX
商品名称：XXX
二、药品成分
本品主要成分为XXX，其他辅料为XXX。

三、适用范围
适用于XXX症状的缓解和治疗。

四、药理作用
本品通过XXX作用于XXX，从而达到XXX的目的。

五、用法用量
1. 成人：每次XXX mg，每日X次。

2. 儿童：请咨询医生。

六、不良反应
1. 常见不良反应为XXX，XXX，XXX等。

2. 严重不良反应请立即停药并就医。

七、禁忌症
1. 对本品过敏者禁用。

2. 对XXX有过敏史者禁用。

3. 其他禁忌症请咨询医生。

八、注意事项
1. 本品不宜长期连续使用。

2. 操作机器、驾驶车辆等需要警觉的活动时慎用。

3. 与其他药物同时使用时请咨询医生。

4. 孕妇、哺乳期妇女和儿童慎用。

九、药物相互作用
1. 本品与XXX同时使用可能增加/减弱其效果。

2. 与其他药物同时使用时请咨询医生。

十、贮藏
密封，置阴凉干燥处保存。

十一、包装
XXXmg/片，X片/盒。

XX生物宣传片脚本(客户确认)(分镜头设计)

多彩的XX，多彩的生活
XXXX生物电子技术有限公司宣传片脚本
生命之光篇——目录
一、开篇——希望之光，开启彩色篇章
二、中篇——生机无限，诠释健康梦想——企业诠释
三、推进——与时俱进，突破健康渴望——实力展示
四、高潮——锐意创新，书写生命传奇——产品描述
五、尾篇——厚德载物，激荡生命舞台——精神内涵
六、结尾——高瞻远瞩，规划七彩未来——展望未来
一、主题线索：
体现企业技术实力，基于对生命的尊重，对健康、快乐生活的追求和向往，专业性、权威性和高度的社会责任感的结晶提炼——多彩极光
二、创作要求
三、项目分析
健康技术责任
XXXX生物电子技术有限公司成立于XXXX年，至今已有XX年历史。

公司一直以技术创新为先导，以服务大众健康为核心理念。

凭借着精湛的技术实力和优秀的管理团队，公司迅速成为XX市高新技术企业，国家高技术研究发展计划（“863”计划）支持企业。

公司秉承以患者需求为己任，尽心尽力服务社会、回报社会的经营宗旨，体现了勇于追求创新的企业内涵和尊重生命热爱生活的企业精神。

四、创意脚本。