
Balance XPR603SNDR
Go Beyond Weighing. Excellence XPR Precisions Balance, 610 g / 120 g capacity, 0.1 mg / 1 mg readability, without draft shield, SmartPanTM weighing pan, 7 inch capacitive colored touchscreen with modern user interface, QM; data integrity and LabX.
Accurate analytical results
XPR balances deliver the accurate weighing results you need as the foundation for your analytical results.
Flexible Solutions
Innovative features and easy to connect accessories meet the needs of almost any application - today and tomorrow.
Easy compliance
Quality assurance features ensure your weighing results are always valid, helping you to comply with even the strictest regulations.
Maximum Capacity | 120 g/610 g |
Readability | 1 mg;10 mg |
Repeatability (typical) | 0.8 mg;4 mg |
Minimum Weight (USP), Typical | 1.6 g |
Weighing Pan Dimensions (DxW) | 127 mm x 127 mm |
Linearity ± | 6 mg |
Repeatability (Test Weight) | 1 mg;6 mg (100 g) |
Settling Time | 1.5 s |
Dimensions (DxHxW) | 411 mm x 102 mm x 194 mm |
Adjustment | Internal / proFACT Advanced |
Linearity | 6 mg |
Material Number(s) | 30316529 |
Data integrity made easy
LabX automatically saves all results and process information securely in a central database. This ensures traceability and assists with FDA 21 CFR part 11 compliance.

Fewer process steps
Under standard conditions, 1 mg readability balances with SmartPanTM can be used without a draft shield. The built-in notepad automatically records all task parameters and results, eliminating manual transcription.

Fast and accurate results
The extraordinary stability provided by SmartPan means you get your results up to twice as fast compared to a standard weighing pan.

Simplified workflows
Add accessories when you want to meet the changing needs of all your different applications e.g. a remote switch or terminal stand. Easy connectivity makes it quick to add peripheral devices such as a barcode reader and/ or label printer.

Stored weighing methods
To ensure consistent processes, store regularly used task methods in your own method library and re-call them anytime you need them.

SOP user guidance
LabX provides full SOP user guidance on the balance so you can be sure that all users follow the same procedures. All QA functions can be managed centrally by LabX, including cheduling routine tests and blocking the balance from use if necessary.

A balance for every need
With readability from 0.1 mg to 1 g and capacity from 200 g to 64 kg, there’s an XPR balance to suit every application.

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我们公司想组建一个新的实验平台,仪器设备都得我们自己选,请问哪位有好点的分析天平(万一之一)推荐的,谢谢了。
1251分析天平称重提到:电子分析天平有基于所用负载的内部校准系统。此校准适用于当前的环境温度。
<41>砝码与天平里面提到:2级砝码用于内置砝码的分析天平的校准工作,以及用于日常分析工作的实验室砝码。
但是看到一份培训资料,说美国fda不认可电子天平的自校系统的校验。
希望了解的战友执教,天平的自校和外置砝码校验是否都被fda接受。
谢谢
我们公司是生物制药公司,最近购买了一台百万分之一天平,还未校正,想请教各位大牛,百万分之一天平如何校正,是否必须由计量局校正?制药行业有没有相关法规文件规定必须得校正?如果有,麻烦分享一下,谢谢!
精确称量与天平合规性管理—张忠任2017.8.2
精确称量与天平合规性管理—张忠任2017.8.2.pdf(5364.43k)
精确称量与天平合规性管理—张忠任2017.8.2.rar(81743.24k)
请问,临床前研究用的电子天平,需要符合GMP要求吗?需要3Q认证吗?相关数据用于申报临床试验的,谢谢
QC实验室的电子天平配有打印机,早已不是什么业界的新闻了。瑞士梅特勒-托利多公司的和德国赛多利斯等国际知名电子天平生产商在N年前(不夸张地说,20年前)就给电子天平配置了打印机,并且电子天平也可以和计算机相连接,将称量数据保存在计算机中。
我国的很多大药企和经过FDA、欧盟认证的药企,基本上都为电子天平配置了打印机和(或者)计算机,将称量数据及时打印出来,和(或者0将称量数据存储在计算机中。
电子天平配置打印机的目的是为了将打印数据及时打印出来,防止称量数据被丢失和人为的改动,或者称量数据不原始(有很多人习惯先将称量数据记录在本上或者纸上,然后在记录在正式的记录上,这也是符合TCH和cGMP的要求的。
我们为电子天平配置上打印机就能做到称量数据真实了吗?我说不一定。当然主流是操作人员会把称量数据及时真实地打印出来。非主流还是可以对称量数据可以做手脚的。为什么这样说?因为如果实验室没有LIMS系统,那么你的电子天平是独立的,操作也是独立的,没有被监视和控制。因为称量操作也会发生失败(比如称量结果超出称量范围或者称量完必,在称量物质转移时发生洒落等现象)。操作人员势必会重新进行称量,那么上次称量的数据就很可能被删除或者不打印出来。
另外,称量的时间也会被人为地改变。一是改变电子天平上的时间设置,二是改变打印机和(或者)计算机上的时间来做假。
所以,我们在给电子天平配置了打印机和(或者)计算机后,我们还应该有合适的文件或者LIMS系统设置和规定和操作人员、主管等人的权限,使我们的称量操作符合法规的要求。避免和减少差错的发生,是GMP的核心内容之一。
以上内容,仅供同行们参考,如有不妥,欢迎指正。因个人水平有限,写的内容会不全,欢迎朋友们进行补充,坛友们会感谢您的。


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