How to Write An Effective SOP?
An effective SOP writing is necessary for the goods manufacturing process. USFDA in the pharmaceutical Industry, WHO and GMPx all regulatory bodies follow the instructions…
Tag: Free QC Course
Problem Solving
The problem solving technique is vital part of business and manufacturing process. Every business and manufacturing hub have faced a lot of problems. To resolve…
Aseptic Processing
Aseptic processing is a method which is used commercially use in the sterilization of water and steam under the pressure. What will you learn After…
Facility Readiness And Site Round
Facility readiness is associated with risk reduction, curcial plainning and decision making. What will you learn In this course, you will learn about implication of…
How To Behave in Audit Room While Facing Regulatory Inspection
Regulatory inspection is a process of evaluation integrity of data submitted to healthcare authorities like USFDA, CDSCO etc. What will you learn In this course,…
How To Face Audits Questions & Answers
Regulatory inspection is a process of evaluation integrity of data submitted to healthcare authorities like USFDA, CDSCO etc. What will you learn In this course,…
Who is Responsible for Quality?
Quality is a important parameter of any production line. In pharmaceutical companies have more than two departaments investigate for quality test, quality control and quality…
Specimen Collection, Transport and Processing Bacteriology
To isolate and identify bacterial etiological agent(s) in deep-seated pus/wound specimens. What will you learn In this course, you learn about the specimen collection from…
FDA Compliance and Prevent 483s Observation
An FDA Form 483 is issued to firm management at the conclusion of an inspection when an investigator has observed any conditions that in their…
How to Respond to Audit Observation
The audit observation is the most important part of an audit report. It represents the end result of weeks of reviews, analysis, interviews and discussions. What…