typical-gmp-documentation-in-a-quality-control-laboratory 
GMPSOP
APRIL 3, 2023
In other word, you need GMP documentation specially developed and used for your laboratory to guide you through everything you do in the lab. Every laboratory facility has unique functions, equipment and facility layout. Depending on the objective of the lab, the need for GMP documentation will change for the laboratory.
GMPSOP
MAY 17, 2024
GMP cleaning and sanitation practices in pharmaceuticals Pharmaceuticals quality assurance & validation procedures GMPSOP %title% Prev PREVIOUS POST GMP cleaning and sanitation of pharmaceutical equipment and facilities account for almost one-third of all production activities, if not more.
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GMPSOP
FEBRUARY 10, 2024
It is a GMP/ GLP requirement that all personnel be trained in the work appropriate to their role. FDA-regulated industries should prepare GMP Training policies and procedures for their employees outlining training approaches, scope, responsibilities and overall training system. Additional documents are included each month.
GMPSOP
MAY 26, 2023
Six steps process to implement change control management Pharmaceuticals quality assurance & validation procedures GMPSOP Six steps process to implement change control management Last modified: June 3, 2023 Table of Contents “It is not the strongest of the species that survive, nor the most intelligent, but the one most responsive to change”.
GMPSOP
MAY 26, 2023
Six steps process to implement change control management Pharmaceuticals quality assurance & validation procedures GMPSOP Six steps process to implement change control management Last modified: May 28, 2023 Table of Contents “It is not the strongest of the species that survive, nor the most intelligent, but the one most responsive to change”.
GMPSOP
FEBRUARY 28, 2024
Basic cleaning and sanitation practices in Pharmaceuticals Pharmaceuticals quality assurance & validation procedures GMPSOP %title% Prev PREVIOUS POST Cleaning and sanitation of pharmaceutical equipment and facilities account for almost one-third of all production activities, if not more. Equipment cleaning and maintenance. (a)
GMPSOP
AUGUST 14, 2023
Pharmaceuticals quality assurance & validation procedures GMPSOP How to perform periodic review of systems and processes in pharmaceuticals? The quality and safety of your products are guaranteed! The quality and safety of your product will suffer immensely. Doesn’t it sound like an ideal world? Sounds too good to be true.
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