FDA form 483 and Warning Letter| What is the difference? 

Q1- A Q2- True It was short, sweet and informative video. I request you to develop and post multiple videos including but not limited to PQC, FAR, stability, FDA audit process etc…

Good information

Very good information

Grt Information

Excellent 👌

Perfectly explained

Thank You Ma'am

Informative, Please refer a session regarding risk assessments...

Awesome

Excellent👍 Kindly make video on Risk assessment

Nice

Good

How to decide in multi step reaction which solvents to test for.

True

Nice... Thank you. I request you to make video in on content of ANDA for different type of formulation. What documents are required. How to fill form and prepare cover letter etc

I want to learn mechanism of all qc instrument,i mean how can any instrument work . by the way this clip was nice for learning purpose . Thanku very much

Plz tell about ich impurity guidlines and thersolds

Please make video starting to End means included each and every Instrument or machine and documentation work. Person who are fresher in Ur channel. they can understand mechanism and system. That is beneficial in interview for them. I am interested to see video of QC , production and packing Department department

very usefull

Tell about Q3 D elementary impurities

Very useful. If possible plz make a video about difference between FDA & MHRA oos guidance

Can u please share info about nce-1 filings

true

Tell me about Q3 guide line

1. form 483

483 True

1

1. 483 form

For more information on FDA form no 482,483 and 484 watch my video

Self based not employee targated

Tell about 21cfr

I want to know the whole process from drug discovery to final Formulation product...

Bad experience

Good information

True