6 Important Tips for calibrating pH Meter

It is critical for pH measurements to be reliable in numerous processes. Industries like agriculture, food processing or even wastewater facility rely on measuring pH accurately to determine the efficiency of a process or quality of a product. One of the key steps in achieving accurate pH results includes pH meter calibration. You must also […]

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How to Maintain and Determine Calibration Frequency of Equipment

The quality of the products manufactured by any enterprise can directly be associated with the accuracy of the instruments producing them. If the instruments are not calibrated properly, or if they are damaged and need repair work, they will surely affect the end products. ISO calibration lists out the general requirements for the competence of […]

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Principles and Importance of Process Control System Validation

Process control system validation as the name suggests is a set of activities which are carried out to check the efficacy of a process control system. It could be a piece of software or hardware which has been introduced to automate a certain process, which needs validation. Alternately, it could be a set of steps […]

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4 Types of Process Validation in Relation to Production

Process validation is a critical part of quality assurance procedures, for practically any sector or industry today. You can perform process validation at various stages of the production lifecycle to confirm whether your process is effectively controlling the quality of your finished product. Based on the stage of the production lifecycle at which process validation […]

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Infographic On Equipment Validation Process

Process and Equipment Validation is a method to establish evidence that a product is produced that meets the predetermined specifications. When a new machine or equipment is acquired, a master validation plan is designed to test the functional specifications and other user requirements. As a part of the validation process, qualification tests are carried out […]

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Equipment Qualification for Analytical Laboratory Instruments

Any instrument that is used in the pharmaceutical industries, small laboratories and health care industries is required to always provide reliable and accurate data. Accuracy and integrity of an instrument is established through qualification, calibration and validation. This is very important for all analytical lab instruments, and for everyone in this industry who makes use of such equipment. […]

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What is IQ OQ PQ?

For industries involved in pharmaceutical and health care products, or even laboratories, product quality is paramount and minute inconsistencies can have disastrous results. Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ) are an essential part of quality assurance through equipment validation. What Do IQ, OQ and PQ Mean? IQ OQ PQ protocols are […]

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What is Electronic Calibration?

If you use any equipment for measurement, then you should get acquainted with calibration. Even the most precise measurement instruments need to be calibrated in order to avoid errors in measurements and ensure accuracy. What is calibration?  – Electronic calibration definition Calibration is checking the accuracy of a measurement instrument by comparing it to reference standards. The result of equipment […]

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Equipment Validation Explained

Equipment validation is a term used to describe a set of independent procedures that are used to check if a product meets the specifications and requirements of its intended purposes. Regulatory agencies around the world have strict requirements for quality, procedures, performance testing, safety checks and the like, for a wide range of products. The […]

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RS Passes Annual ISO Audit

RS Calibration Services is proud to announce it has again successfully passed the annual International Organization for Standardization (ISO) Audits. The annual surveillance audit, performed by SAI Global, is necessary for the company to maintain ISO 9001:2008 certification. The audit, performed on December 4, is designed to assure continuing compliance and full evaluation of requirements. […]

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