Scientific Instruments Calibration

Conheça conteúdos de destaque no LinkedIn criados por especialistas.

  • Ver perfil de Deepthi Rathnayake

    Chemist | Lab Technician, Quality Officer - Water, Food, Fertilizer, Cosmetic, Oil, Pharmaceutical

    4.199 seguidores

    Brief explanation about a refractometer 1. What Is Brix? Brix (°Bx) is a unit that measures the percentage of soluble solids (mostly sugars) in a liquid. • 1°Bx = 1 gram of sucrose in 100 grams of solution. Brix is commonly used in: • Food and beverage industry (juice, wine, soft drinks) • Agriculture (fruits and vegetables) • Cosmetics (to measure concentration of sugar-based solutions) 2. Principle of Refractometer A refractometer works on the principle of light refraction. • When light passes from one medium (air) into another (liquid), it bends. • The amount of bending depends on the refractive index of the liquid. • The refractive index changes with the concentration of solutes (like sugar). • The refractometer converts this refractive index into a Brix percentage. 3. Types of Refractometers 1. Handheld Analog Refractometer • Simple and portable • Requires manual reading through an eyepiece 2. Digital Refractometer • More accurate and easier to read • Displays the Brix value on a digital screen 3. In-line Process Refractometers • Installed in industrial pipelines for continuous monitoring. 4. Guide to Measuring Brix with a Refractometer A. Calibration (Important Before Use) 1. Clean the prism with distilled water. 2. Add a few drops of distilled water. 3. Close the daylight plate and look through the eyepiece (or press the button on a digital model). 4. Adjust the scale to read 0.0 Brix. 5. Wipe the prism dry. B. Sample Testing 1. Add 1–2 drops of the sample liquid onto the prism. 2. Close the daylight plate gently (no air bubbles). 3. Hold it up to a light source. 4. Look through the eyepiece (analog) or press the button (digital). 5. Read the Brix value at the line where the blue and white areas meet. C. Cleaning • After testing, clean the prism with distilled water and dry it with a soft tissue to avoid contamination. 5. Tips for Accurate Results • Use room temperature samples. • Avoid air bubbles or particles in the liquid. • Regularly calibrate your refractometer. • Do not use strong acids or solvents on the prism.

  • Ver perfil de Vinod Yadav

    Pharma Quality Control ! HPLC !Uv visible spectrophotometer

    8.078 seguidores

    If your HPLC calibration is weak, your data is already wrong — even before analysis starts. Most analysts run HPLC daily… but very few truly understand ALL calibration parameters Save this post — it’s a complete QC checklist 👇 HPLC CALIBRATION – ALL PARAMETERS YOU MUST CHECK 1️⃣ PUMP (Solvent Delivery System) Flow rate accuracy: ± 2.0% Flow rate precision: %RSD ≤ 1.0% Pressure accuracy: ± 10% Gradient accuracy: ± 2.0% (if applicable) Gradient precision: %RSD ≤ 2.0% 2️⃣ INJECTOR / AUTO-SAMPLER Injection volume accuracy: ± 2.0% Injection precision: %RSD ≤ 1.0% Carryover: ≤ 0.1% of standard response 3️⃣ DETECTOR (UV / PDA) Wavelength accuracy: ± 2 nm Wavelength precision: ± 1 nm Detector linearity: r ≥ 0.999 Noise & drift: As per SOP / manufacturer 4️⃣ COLUMN OVEN (If Used) Temperature accuracy: ± 2°C Temperature precision: ± 1°C 5️⃣ SYSTEM PERFORMANCE System precision: %RSD ≤ 2.0% Retention time precision: %RSD ≤ 1.0% Resolution (if applicable): ≥ 2.0 6️⃣ SOFTWARE & DATA INTEGRITY Integration accuracy Audit trail enabled 21 CFR Part 11 compliance Secure data backup PRECAUTIONS YOU SHOULD NEVER IGNORE Use fresh & filtered mobile phase Proper degassing is mandatory Remove air bubbles from pump lines Allow system equilibration Use calibrated balance & stopwatch Document every step clearly GUIDELINE REFERENCES USP <621> – Chromatography USP <1058> – Analytical Instrument Qualification ICH Q2 (R2) EU GMP Annex 15 Calibration is not a formality. It is the foundation of trust in your data. Follow Learn with Vinod For practical pharma QC knowledge That actually helps you in the lab #HPLC #Calibration #PharmaQC #QualityControl #AnalyticalChemistry #USP #ICH #GMP #LearnWithVinod

  • Ver perfil de FT Roopam Jangra

    Food Safety & Quality Executive | Qualified: ICAR JRF/SRF 2023 AIR RANK 41, | HACCP | ISO 22000:2018 | ISO/IEC 17025:2017 | FSSAI Compliance

    1.546 seguidores

    🔬 Are Your pH Readings Truly Accurate? Here’s the Secret: Proper Calibration! In the world of food quality, pharmaceuticals, and laboratories, even a small error in pH can lead to big consequences. That’s why pH meter calibration isn’t just a routine—it’s a critical control step. Here’s a simple yet powerful guide to get it right 👇 🧪 Step-by-Step pH Meter Calibration: ✅ 1. Start Clean Rinse the electrode with distilled water and gently blot dry (never rub!). ✅ 2. First Point – Neutral (pH 7.00) Place the electrode in pH 7 buffer solution. Wait for stabilization and set the calibration. ✅ 3. Second Point – Acidic or Alkaline Use pH 4.00 (acidic) or pH 10.00 (alkaline), depending on your sample. Allow the reading to stabilize and confirm calibration. ✅ 4. Triple Calibration (Best Practice) For higher accuracy, use all three buffers: 4.00, 7.00, and 10.00. ✅ 5. Rinse Between Steps Always rinse and blot the electrode before moving to the next buffer. ⚠️ Common Mistakes to Avoid: ❌ Using expired or contaminated buffer solutions ❌ Skipping calibration before important analysis ❌ Letting the electrode dry out ❌ Wiping the electrode harshly 💡 Pro Tips: ✔️ Calibrate daily for critical work ✔️ Use fresh buffers every time ✔️ Store the electrode in proper storage solution ✔️ Ensure temperature consistency (or use ATC) 🎯 Remember: “An uncalibrated pH meter is worse than no measurement at all.” Accuracy begins with calibration. Make it a habit, not an option. #QualityControl #FoodSafety #LaboratoryPractice #pHMeter #Calibration #FoodIndustry #AnalyticalChemistry

  • Ver perfil de Abderrakib Ghettas

    Instrumentation and Control Engineer chez Sonatrach

    1.819 seguidores

    🔧 7 Steps Calibration Procedure for Differential Pressure (DP) Transmitters : Ensuring accurate measurement is key to process safety, product quality, and operational efficiency. Here's a simplified yet professional approach to calibrating a DP transmitter, aligned with NIST traceability and IEC 61508 functional safety standards: ✅ Step 1: Prepare Tools Required Calibrated pressure source (hand pump) Digital pressure calibrator or reference manometer Multimeter, power supply (24V), HART communicator Manufacturer’s datasheet and calibration certificate ✅ Step 2: Safety First Follow site-specific LOTO (Lockout-Tagout) procedures Depressurize lines and isolate process connections Wear appropriate PPE and ensure proper venting ✅ Step 3: Setup the Calibration Bench Connect transmitter to the pressure source and reference device Apply 24 VDC power and ensure correct wiring ✅ Step 4: Perform Calibration Apply zero pressure (LRV) → Adjust Zero Apply Span pressure (URV) → Adjust Span Repeat in 25% steps (0%, 25%, 50%, 75%, 100%) ✅ Step 5: Check Linearity Record readings at each pressure point in both ascending and descending order Compare against reference device Ensure readings are within manufacturer’s accuracy specs ✅ Step 6: Post Calibration Checks Reconnect to process carefully Remove test equipment Confirm transmitter is responding correctly in DCS or PLC ✅ Step 7: Calibration Report Preparation Document: Instrument tag As-found and as-left values Date/time, environmental conditions Name and signature Ensure traceability to NIST standards Align with IEC 61508 if part of a SIS loop Let’s raise the standard in field instrumentation #Instrumentation #DCS #Calibration #ProcessControl #Maintenance #Automation #DPTransmitter #IEC61508 #NIST

  • Ver perfil de Rahul Chaurasiya

    Senior Laboratory Technologist | QC & Report Accuracy Specialist | Helping Labs Reduce Wrong Reports & Improve Patient Safety

    4.541 seguidores

    If You Don’t Use Westgard Rules, You Are Guessing — Not Doing Quality Control Most laboratories check only one thing: “Is QC within ±2SD?” But that is not Quality Control. That is only noise checking. The real job of QC is to detect: • hidden bias • slow drift • random errors • reagent and calibration problems Before they reach the patient. That is exactly what Westgard Rules do. I created this step-by-step visual chart to show: • When to apply Westgard Rules • What each rule means • Which errors are random vs systematic • When to accept a run • When to stop reporting immediately One ignored rule can silently allow hundreds of wrong reports to be released. One Westgard violation = One Stop. If you work in: Biochemistry, Immunoassay, Hematology, or Lab QA — this chart should be on your wall. Save it. Share it with your lab team. And use it to protect patient safety. #WestgardRules #QualityControl #MedicalLaboratory #LabTechnologist #ClinicalChemistry #Immunoassay #LabQuality #PatientSafety #NABL #CAP #Diagnostics #LaboratoryMedicine #QCChart #HealthcareQuality Follow us to become a Quality Control expert — build confidence, protect patient safety, and grow your professional laboratory career.

  • Ver perfil de Shahid Sheikh

    Lead ICSS Engineer - Instrumentation & Control

    22.388 seguidores

    🌡 1. Purpose of Calibration Calibration ensures the temperature transmitter accurately converts the sensor signal (RTD/Thermocouple) into a standard output signal (usually 4–20 mA). It verifies and adjusts the transmitter’s accuracy against a known reference. --- 🧰 2. Required Tools & Equipment Temperature source (Dry Block Calibrator / Temperature Bath) Reference thermometer (high-accuracy, traceable standard) Multimeter / Loop calibrator (to measure 4–20 mA) Power supply (usually 24 V DC) HART communicator (if it’s a smart transmitter) Manufacturer’s datasheet or calibration sheet --- 🧪 3. Calibration Procedure Step 1: Preparation Isolate the transmitter from the process. Ensure safety: depressurize if needed, wear PPE. Connect transmitter to power supply and loop calibrator. Insert sensor or transmitter’s probe into the temperature source. --- Step 2: Apply Test Points Choose 3 to 5 calibration points, typically: 0% (Lower Range) → e.g., 0 °C 25% 50% (Mid Range) → e.g., 50 °C 75% 100% (Upper Range) → e.g., 100 °C For each point: 1. Set the temperature source to the reference value. 2. Allow stabilization. 3. Record: Reference temperature Transmitter’s indicated temperature mA output --- Step 3: Verification & Adjustment Compare measured output vs. expected output. If within tolerance, record as “As Found” and no adjustment needed. If out of tolerance, use: Zero & span adjustments (analog) HART communicator or software (smart transmitters) Repeat test points after adjustment (“As Left”) to confirm accuracy. --- 📊 4. Acceptance Criteria Error must be within manufacturer’s specification (e.g., ±0.1 % of span). Both upscale and downscale readings should be checked for hysteresis. --- 📝 5. Documentation Record the following: Instrument tag number Calibration date & technician name Reference equipment used As-found & as-left readings Adjustment details Next due date --- 🛠 6. Types of Temperature Transmitters Type Input Output Common Use RTD Transmitter Resistance (Pt100 etc.) 4–20 mA / Digital Precise temperature measurement Thermocouple Transmitter mV signal 4–20 mA / Digital High temp ranges, industrial Smart / HART Transmitter RTD / TC 4–20 mA + HART Advanced diagnostics & remote config

    • + 1
  • Ver perfil de Md. Moniruzzaman Monir

    Executive, Quality Control

    749 seguidores

    📕 Validation / Verification / Calibration / Qualification.. ✅ 1. Validation Definition: A documented process of proving that a method, system, or process consistently produces results meeting predetermined acceptance criteria. Example: Analytical Method Validation: Proving that an HPLC assay method is accurate, precise, specific, robust, etc. Process Validation: Running three consecutive commercial batches of a tablet to demonstrate consistent quality. ✅ 2. Verification Definition: The act of checking whether a specific requirement or specification has been fulfilled. (Validation = proving overall reliability, Verification = checking individual requirements) Example: Measuring buffer pH with a calibrated pH meter to confirm it meets specification (e.g., pH 7.0 ± 0.05). Checking whether a dissolution apparatus is running at the set speed of 50 rpm. ✅ 3. Calibration Definition: The process of comparing an instrument’s measurements to a known standard and adjusting it if necessary. Example: Checking an analytical balance using a 100 g standard weight to see if it reads exactly 100.00 g. UV spectrophotometer calibration using standard potassium dichromate solution to confirm correct absorbance. ✅ 4. Qualification Definition: A documented process of demonstrating that equipment or systems are properly installed, operate correctly, and perform as intended for their specific use. Example: HPLC System Qualification: IQ (Installation Qualification): Ensuring the HPLC system is installed properly. OQ (Operational Qualification): Confirming it operates correctly under defined conditions. PQ (Performance Qualification): Running real samples to demonstrate acceptable performance in routine use. 📌 In Short: Validation → Proves the process is reliable. Verification → Confirms a specific requirement is met. Calibration → Adjusts instrument readings against standards. Qualification → Demonstrates equipment/system is suitable for intended use.

  • Ver perfil de Aman Gupta

    Microbiologist

    2.474 seguidores

    🔬 pH Meter Verification and Validation in Pharma Industry In pharmaceutical laboratories, accuracy and reliability of analytical instruments are essential — and one such critical instrument is the pH meter. ✅ Verification Verification ensures that the pH meter is working correctly on a daily or routine basis. It is usually done by calibrating the instrument using standard buffer solutions (e.g., pH 4.0, 7.0, and 9.2) and checking that readings are within the acceptable range. 👉 This confirms instrument performance before analysis. ✅ Validation Validation, on the other hand, provides documented evidence that the pH meter consistently produces accurate and reproducible results throughout its intended use. It includes checking parameters like: Linearity,Accuracy,Precision,Range, Specificity and Robustness. ⚙️ Best Practices: Calibrate regularly using fresh buffer solutions. Clean electrode properly after each use. Maintain documentation of verification and validation reports. 📋 Proper verification and validation not only ensure data integrity but also maintain regulatory compliance (as per WHO, USP, and GMP guidelines). 💡 Regular verification + well-documented Validation = Reliable pH measurement = Quality assurance! #Pharma #QualityControl #pHMeter #Validation #GMP #Laboratory #PharmaceuticalIndustry #Calibration

  • Ver perfil de Gugan Bharath M

    Junior Instrumentation Engineer @Sime

    1.436 seguidores

    🔹Loop Checking ≠ Calibration🔹 In industrial automation, calibration and loop checking are often mistaken as the same — but they’re very different. ✅ Calibration ▫️Verifies transmitter accuracy against a known standard. ▫️Input: pressure, temperature, or electrical signal. ▫️Adjust zero/span as needed. ▫️Focus: instrument performance. ✅ Loop Check ▫️Validates the entire control loop from field device to DCS/PLC. ▫️Signal injection → confirm correct value in the control system. ▫️Verifies scaling, polarity, wiring, and logic mapping. ▫️Focus: signal integrity across the loop. 👉 A transmitter may be perfectly calibrated yet fail loop checking due to: →Incorrect PLC/DCS configuration, →Mis wired signal cable, →Faulty I/O channel. ⚡ Commissioning Best Practice 1️⃣ Calibrate instruments (field or workshop). 2️⃣ Perform loop checks before startup. ✅ This workflow prevents delays, ensures system reliability, and reduces troubleshooting hours. #loopchecks #calibration #instrumentation #automation #controlsystems #engineering

Conhecer categorias