Why Production Fails?
Production is the most important part of any company. In daily activity in the company, lot of reasons behind production failure. Failure can be a…
Tag: Free Manufacturing Course
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…
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,…
Why FDA Regulatory Inspection Comes?
FDA may conduct an regulatory inspection of your operation for a variety of reasons, such as a routinely scheduled investigation, a survey, or a response…
Human Error Reduction
Human error reduction must be a primary focus of management in healthcare organizations. Human error is responsible for more than 80 percent of failures and…
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…
Trending of Breakdown in Equipment
Breakdown maintenance is maintenance performed on a piece of equipment that has broken down, faulted, or otherwise cannot be operated. The goal of breakdown-maintenance is…
Gemba Walk In Pharma Industry
Gemba Kaizen is a Japanese concept of continuous improvement designed for enhancing processes and reducing waste. What will you learn In this course, you will learn…