FAR || Field Alert Report || USFDA Guideline ||

List of the Pills in Video
00:00 Introduction
01:09 What is a FAR?
01:40 Which type failures can trigger FAR
02:12 Within how many days we need to submit FAR?
03:00 What will happen if not submitting FAR?
03:45 What is Initial, follow up & Final FAR?
04:30 If product not distributed and OOS observed in that case FAR required?
04:49 If OOS results invalidated within 3 days ,do FAR required?
05:23 When Final FAR should be submitted?
05:34 How to submit FAR?
06:03 Who is responsible for submitting FAR?
06:35 Is FAR required if recall is initiated?
Happy Learning
Pharma Pill

[@vps1705]

Excellent informative

[@dharshanyappo152]

Sir urs explaination is very understanding it will reach all level of person

[@sanjays1344]

Thanks, informative

[@PharmaPill]

Glad it was helpful!

[@manojmodi414]

Good morning sir

[@kausalbhavsar8153]

Fantastic video

[@ramakrishnaguttula7941]

Good video, please post more pharma videos

[@manojmodi414]

Dear sir,
Your video is knowledgeable
Kindly prepare for GLP related videos

[@ramakrishnaguttula7941]

Good information

[@PharmaPill]

Thanks Ramakrishna Garu … :)

[@Creativeworld1103]

Very nicely explained.FAR is for USFDA what about other regulatory .Can you please prepare , how to inform to other regulatory in case of failure.

[@patilmahavira]

Pls tell about process of new and old analytical instrument validation, qualifications and calibration and their flow and procedure

[@manojmodi414]

Please prepare a video on warning letter

[@PharmaPill]

Okay

[@manojmodi414]

FEI