Mark foster - QMS Advisor

Energy Conservation Policy for QMS Advisors in the Pharmaceutical Industry

June 16, 2024 by Mark foster

Introduction Energy conservation is crucial for sustainability and operational efficiency within the pharmaceutical industry. QMS Advisors acknowledges its responsibility to minimize environmental impact through effective energy management. This policy outlines our commitment to conserving energy resources in accordance with international standards and regulations. Policy Statement At QMS Advisors, we recognize that energy conservation plays a … Read more

Standard Operating Procedure for calibration of analytical balance

June 16, 2024June 16, 2024 by Mark foster

Standard Operating Procedure for calibration of analytical balance Current Version 01 Controlled # SP-001 Effective Date: Distribution: Revision History: Review # Revision # Date Authorizer Reason 00 00 Date:01 Name of Authorizer Document Created 1.0 Objective: The purpose of this SOP is to describe the procedure of Calibration of Analytical weighing balance in the … Read more

Standard Operating Procedure for Analytical Balance 220g x 0.1mg Radwag AS 220/C/2.

June 16, 2024 by Mark foster

Standard Operating Procedure for Analytical Balance Current Version 01 Controlled # SP-001 Effective Date: Distribution: Revision History: Review # Revision # Date Authorizer Reason 00 00 Date:01 Name of Authorizer Document Created 1.0 Objective: The purpose of this SOP is to describe the procedure of Operation, Calibration, and Maintenance of Analytical balance (Analytical Balance … Read more

Standard Operating Procedure for UV Spectrophotometer (Manual Use), Shimadzu UV-1800

June 15, 2024 by Mark foster

Purpose The purpose of this procedure is to describe the operating procedure of UV-Spectrophotometer Shimadzu, UV-1800. Scope and Application This procedure applies to all UV-Spectrophotometers Shimadzu, UV-1800 in the Laboratory. Responsibility Tasks Responsibility Responsible to perform all the activities as per the SP and to maintain and record all the activities as per the SP. … Read more

Calibration and Validation in Pharmaceutical Quality Control

June 2, 2024 by Mark foster

Calibration VS Validation an Overview The pharmaceutical industry has a big job: making sure medicines are safe and work well for millions of people around the world. To do this, they have strict rules to follow called quality control. Calibration and validation are super important parts of this process. They help make sure medicines are … Read more

ALCOA and ALCOA Plus Principles for Data Integrity

July 1, 2024May 6, 2024 by Mark foster

9 Principles for Data Integrity Welcome to the world of ALCOA, a powerful tool that has transformed the landscape of data integrity in pharmaceutical manufacturing facilities. But what exactly is ALCOA, and why is it so crucial in the realm of pharmaceuticals? ALCOA, an acronym for Attributable, Legible, Contemporaneous, Original, and Accurate, serves as a … Read more

ALCOA Data Integrity

July 1, 2024May 6, 2024 by Mark foster

Data integrity is the maintenance of, and the assurance of, data accuracy and consistency over its entire life-cycle. The GxP’s require manufacturers and distributors of medicinal products to apply the Data Integrity principles to the data they generate.