HANDLING OF DATA INTEGRITY
HANDLING OF DATA INTEGRITY PURPOSE: To lay down a procedure for management of data generated through electronic and paper based systems
Read MoreQuestion & Answer on Quality Control Part -III AS PER EU Guidelines (EudraLex)
Question & Answer on Quality Control Part -III AS PER EU Guidelines (EudraLex) Question: What is the purpose of the
Read MoreQuestion & Answer on Quality Control Part -II AS PER EU Guidelines (EudraLex)
Question & Answer on Quality Control Part II AS PER EU Guidelines (EudraLex) Question: What validation is required for testing
Read MoreOperation & cleaning of Non-viable Particle counter
Operation & cleaning of Non-viable Particle counter PURPOSE To lay down the procedure for operation & cleaning of non-viable particle counter.
Read MoreEntry & Exit procedure for manufacturing room of SVP section
Entry & Exit procedure for manufacturing room of SVP section PURPOSE: To lay down the written procedure for entry &
Read MoreQuestion & Answer on Quality Control Part -I AS PER EU Guidelines (EudraLex)
Question & Answer on Quality Control AS PER EU Guidelines (EudraLex) Question: What does Quality Control involve, and why is
Read MoreStainless Steel
Stainless Steel From time to time, stainless steel (SS) became a material that quickly adapted to use in many industries,
Read MorePROCEDURE FOR CLEANING,OPERATION AND CALIBRATION OF MICROMETER SCREW
PROCEDURE FOR CLEANING,OPERATION AND CALIBRATION OF MICROMETER SCREW PURPOSE To lay down a procedure for Operation and calibration of micrometer
Read MoreTachometer
Tachometer PURPOSE To lay down a procedure for Cleaning, Operation and Calibration of Tachometer. SCOPE This procedure is applicable for
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Filter Integrity in Clean Rooms of Pharmaceuticals
Filter Integrity in Clean Rooms of Pharmaceuticals Clean rooms are critical environments in the pharmaceutical industry where products are manufactured,
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Quality Assurances Quiz
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DEPYROGENATION OF GLASSWARE USED FOR BACTERIAL ENDOTOXIN TEST IN MICROBIOLOGY LAB
DEPYROGENATION OF GLASSWARE USED FOR BACTERIAL ENDOTOXIN TEST IN MICROBIOLOGY LAB Depyrogenation of glassware is a crucial process in pharmaceutical,
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ENTRY AND EXIT PROCEDURE IN MICROBIOLOGY LAB
ENTRY AND EXIT PROCEDURE IN MICROBIOLOGY LAB The entry and exit procedure in a microbiology lab is a critical aspect
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Pharma Change Control
Pharma Change Control Pharma Change Control is inevitable in any organization, but managing changes effectively is crucial to maintain product
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Deviation Management
Deviation Management Deviation Management is a systematic approach used to identify, document, investigate, and resolve deviations from established quality standards
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Market Complaint Handling
Market Complaint Handling Market Complaint Handling is a systematic process that organizations use to collect, evaluate, and resolve complaints or
Read MoreVendor Audit
Vendor Audit Vendor Audit, also known as supplier audit or third-party audit, is a systematic assessment of suppliers or vendors
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Standard Operating Procedures (SOPs) in Pharmaceuticals: Ensuring Quality, Compliance, and Safety
Standard Operating Procedures (SOPs) in Pharmaceuticals: Ensuring Quality, Compliance, and Safety Standard Operating Procedures (SOPs) are a cornerstone of the
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Quality Control in Pharmaceuticals: Ensuring Product Safety and Efficacy
Quality Control in Pharmaceuticals: Ensuring Product Safety and Efficacy Quality control is a critical component of the pharmaceutical industry, focused
Read MoreQuality Assurance in Pharmaceuticals: Ensuring Safe and Effective Medications
Quality Assurance in Pharmaceuticals: Ensuring Safe and Effective Medications Quality assurance is a critical aspect of pharmaceutical manufacturing that ensures
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