instrument-calibration-procedure 
GMPSOP
MARCH 20, 2024
Instrument calibration procedure for pharmaceutical industry Pharmaceuticals quality assurance & validation procedures GMPSOP %title% Last Updated on March 20, 2024 Prev PREVIOUS POST Have you ever wondered if the scales at the grocery checkout show the right amount? The answer is instrument calibration.
GMPSOP
APRIL 3, 2023
To confirm your test results are trustworthy and unbiased, you would turn to well-designed policies, procedures, guidelines, methods, protocols and all types of records. How do you do it? In other word, you need GMP documentation specially developed and used for your laboratory to guide you through everything you do in the lab.
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GMPSOP
DECEMBER 24, 2023
ISO/ IEC 17025: General requirements for the competence of calibration and testing laboratories. All sampling procedures and plans must be documented. General GLP requirements Laboratory activities and procedures must conform to many GLP requirements. – Calibrate and quality instruments.
GMPSOP
FEBRUARY 10, 2024
FDA-regulated industries should prepare GMP Training policies and procedures for their employees outlining training approaches, scope, responsibilities and overall training system. – Audit the system periodically to ensure it complies with the company procedure. General Operating Procedures e.
GMPSOP
JULY 23, 2023
Laboratory Instruments: Including analytical instruments like HPLC systems and spectrophotometers i.e., mass spectrometers. Also, you should include references to the documents to be used, deviation handling, and change management procedure in the protocol.
GMPSOP
MARCH 17, 2023
Table of Contents If you are looking for literary help to write an actionable procedure on corrective and preventive action for your workplace or school, this article will be a good place to start. keep the samples and instruments in their last original positions. Consider this scenario. Ideally, you should halt further testing.
GMPSOP
JULY 14, 2023
What you will need are properly validated equipment cleaning procedures and a well-defined cleaning and verification regime in order to make sure your products are free from unnecessary contaminants. Once you will apply the basic rules in developing your cleaning procedure, you will move one step ahead in assuring product quality and safety.
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