Month: September 2023

Standard Operating Procedure (SOP) for Handling of Spillages in the Laboratory

Explore a comprehensive Standard Operating Procedure (SOP) for the safe and effective handling of spillages in laboratory settings. This SOP provides guidelines for identifying, reporting, and responding to various types of spills, including chemical, biological, and hazardous material spills, ensuring the safety of laboratory personnel and the environment.

Standard Operating Procedure (SOP) for Actions to be Taken for Unusual Observations for Instruments During Calibration

Discover a comprehensive Standard Operating Procedure (SOP) for addressing unusual observations encountered during instrument calibration within your organization. This SOP outlines procedures for recognizing, evaluating, and taking appropriate actions in response to unusual observations to ensure the accuracy and reliability of calibration processes.

Standard Operating Procedure (SOP) for Cleaning of Water Bath

Discover a comprehensive Standard Operating Procedure (SOP) for cleaning and maintaining your laboratory Water Bath equipment. This SOP provides step-by-step guidance on routine cleaning, disinfection, and record-keeping to ensure equipment cleanliness, sample integrity, and contamination prevention within [Company Name].

Standard Operating Procedure (SOP) for Issuance, Maintenance, & Disposal of HPLC/GC Columns

Explore a comprehensive Standard Operating Procedure (SOP) for the issuance, maintenance, and disposal of High-Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC) columns within your organization. This SOP provides clear guidelines for column issuance, handling, storage, maintenance, and proper disposal to ensure accurate and reliable analytical results while adhering to regulatory and safety standards.

Standard Operating Procedure (SOP) for Calibration Program

Explore a comprehensive Standard Operating Procedure (SOP) for establishing and managing a calibration program within your organization. This SOP provides step-by-step guidance on equipment identification, scheduling, execution, record-keeping, and responsibilities to ensure the accuracy and reliability of your measuring and testing equipment in accordance with regulatory requirements.

Start of Pharmaceutical Career: Insider Tips for Fresher-Level R&D Interviews

In the ever-changing world of pharmaceutical research and development (R&D), getting an interview as a newcomer is both exciting and challenging due to fierce competition. To increase your chances of success, thorough preparation is key. In this guide, we will help you understand how to excel in your Fresher-Level R&D Interviews

Standard Operating Procedure (SOP) for Cleaning of Centrifuge

Explore a comprehensive Standard Operating Procedure (SOP) for cleaning and maintaining your laboratory centrifuge equipment. This SOP provides step-by-step guidance on routine cleaning, decontamination, and record-keeping to ensure equipment longevity, prevent contamination, and maintain sample quality within [Company Name].

Standard Operating Procedure (SOP) for Cleaning of Water Purification System

Discover a comprehensive Standard Operating Procedure (SOP) for the cleaning and maintenance of your Water Purification System within [Company Name]. This SOP provides step-by-step guidance on routine cleaning, sanitization, and record-keeping to ensure the production of high-quality purified water and the longevity of your equipment.

Standard Operating Procedure (SOP) for Calibration of Glassware in Pharmaceuticals

Explore a comprehensive Standard Operating Procedure (SOP) for the calibration of glassware in pharmaceutical processes within [Company Name]. This SOP provides step-by-step guidance on glassware calibration, including preliminary checks, calibration setup, the calibration process, and recordkeeping, ensuring accurate and reliable measurements for pharmaceutical operations.

Standard Operating Procedure (SOP) for Operational Qualification of Dissolution Tester

Explore a comprehensive Standard Operating Procedure (SOP) for conducting the Operational Qualification (OQ) of a Dissolution Tester within [Company Name]. This SOP provides step-by-step guidance on the setup, performance verification, and documentation of the OQ process, ensuring the accuracy and reliability of dissolution testing in pharmaceutical quality control.