SOP for Operation and Calibration of Air Flow Meter
SOP for Operation and Calibration of Air Flow Meter: 1.Objective: To lay down a procedure for operation and calibration of Air Flow meter. 2.Scope: This SOP covers the operation and …
Pharmaceutical manufacturing and quality assurance
SOP for Operation and Calibration of Air Flow Meter: 1.Objective: To lay down a procedure for operation and calibration of Air Flow meter. 2.Scope: This SOP covers the operation and …
Clinical Data Management Interview Questions and Answers: Q1: What are the role of the Clinical Data Manager (CDM)? A: It is the responsibility of a clinical data manager to collect …
The term “pharmaceutical tablet” refers to both molded and pressed unit dosage forms of medications that contain one or more active medicinal ingredients. Typically, a tablet consists of a combination …
SOP For Operation procedure for Ice Maker: Objective: To lay down the procedure for the operation of ice maker. Scope: This standard operating procedure covers the operation procedure for ice …
Before starting the clinical trial process flow, we will understand, What is a definition of a clinical trial? what is a clinical trial in pharma? What is a Clinical trial? …
SOP for Disaster management for Chromatographic Software Data System Purpose: This procedure establishes a disaster management plan for handling any natural disaster or a human-made disaster that destroys hardware, software, …
What Is The Difference Between KF And LOD In pharmaceutical quality control, there are different methods to determine the water content or moisture content of the sample. i.e. 1. Karl …
In Pharmaceutical, an Annual product quality review (APQR) is of high importance to summarize the product quality for an improvement or to know the product trends. APQR is also known …
Principle of Turbidity in pharma Turbidity is the optical property, that causes light to be scattered and absorbed, rather than transmitted. The scattering of the light that passes through a …
Types Of FDA Inspections If the organization is manufacturing drugs or drug devices or it is the processor of the USFDA product, then the organization is bind to go through …