Presenting Documents During Regulatory Inspections In Pharma
Pharma regulatory inspections by USFDA & other regulatory agencies are a common scenario in the pharma manufacturing units. The documents presented during these inspections are…
Tag: Free QA Course
Career Tips For Freshers In Pharmaceutical Industry
This course tells you about the various tips which can help you grow faster in pharma industry & also you will learn the do’s &…
Understanding FDA Inspection & Form 482 | Form 483
FDA inspection is a regular phenomenon in pharma manufacturing units. These inspections are very crucial for a pharma manufacturing unit as it may put some…
Importance of Training In Pharma
Training is not a choice but a mandate. Without regular training, you cannot expect your employees involved in Good Manufacturing Practices (GMP) to excel in…
GMP Document Simplification
Good Manufacturing Practices documents can be simplified to Reduce Complexity, Improve Compliance & Productivity. What will you learn How to write Simple SOP Reduce Number…
Basics of SOP Writing In Pharma
Standard operating procedure writing is a set of instructions intended to run routine operations by an organization. What will you learn In this Course, you…
Schedule U Pharma Manufacturing
Schedule U describes the particulars to be shown in manufacturing record. What will you learn You will learn about the how to collect pharmaceutical manufacturing…
How to Face 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,…
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…
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…