Ich trphu International Council harmonisation technical requirements pharmaceutical Human use .. 13 principles; 1ethics declaration of hilsinkey 2 risks versus benefits 3 rights safety and wellbeing 4 non clinical data enough to suport 5 protocol 6 protocol compliance 7 qualifications of the investigator 8 qualifications of the staff members 9 informed Consent 10 clinical trials information 11 confidentiality 12 gmp 13 systems
For a video discussing a topic related to succinctly organizing ICH-GCP, the first two plus minutes feels as though our overloaded truck is about to tip over a cliff without warning. Review and edit. Try re-shooting. Voice each thought one time only. Move to next point.
This was my 1st video ever made on RUclips and 1st video of this channel. Appreciate your suggestions will consider it and I hope the rest all videos on the channel you can see the improvement.
Can you describe simply by denoting giidline name and number along with 21 cfr, anvisa , ich, other guidelines. Means Which guidelines refer to validation, qualification, investigation, risk assessment, change control, deviation, incidents, capa, root cause analysis, sampling techniques, manufacturing and packing, gdp, gmp. Etc Plz awaited for response.
Ok, it will take a while but I will try.... But may I know what comparison u need because all 3 are totally different. Us fda is regulatory agency of US whereas MHRA is for UK, ICH is not 1 particular Regulatory agency of a country. What u want me to compare specify...
Ich trphu
International Council harmonisation technical requirements pharmaceutical
Human use ..
13 principles;
1ethics declaration of hilsinkey
2 risks versus benefits
3 rights safety and wellbeing
4 non clinical data enough to suport
5 protocol
6 protocol compliance
7 qualifications of the investigator
8 qualifications of the staff members
9 informed Consent
10 clinical trials information
11 confidentiality
12 gmp
13 systems
Video starts at 2:16 thank me later
tq
employee of the year]
employee of the year]
Thanks
Thanks
Tq for the detailed information on ICH GCP guidelines .
I dont know how but some how your crazy way worked for me...
Start from 3.19
kindly make comparative video on ich vs usfda vs MHRA
better if with origin story of all
Mam thank you so much......!!!!! It was very nice and useful..... I request you to upload more such videos....
Keep posting.. about clinical research associate
Thanks for good information
Could you please make a video on interview questions n how to prepare for an interview for CR position
wait for 3 more weeks, will soon upload
Tq information is very distinct nd clear
Thanku for sharing this video..i have my interview..it was very confusing to learn..u made it easy 😊👍
Awesome informative video. Thanks for the effort.
Tq so much. Very useful.. make more videos
Thanq sis..
It is easy to learn
Awesome 👍
Thank you.
That was very helpfull thank you for your efforts
Thank you so much
Thank you dear,,,👍👍
It was very good and exhaustive,,,👍
Hiii mam .. recently i got placed in MNC..as a PV trainee.... mam will u please help me in GCP 6 guidelines...
Thanks so much mam
Really helpful info mam
Nice explanation
Mam ICH GCP guidelines : QUALITY , EFFICACY,SAFETY, MULTIDISCIPLINARY.HOW to read and what to read from this.please make video on this.
Rajasree, I appreciate you for asking. Definitely, i will make one video on it soon.
Hello mam please help me cilinical reaserch corse kaise kare
Please check out the videos on channel, has mentioned already.☺️
Iam soo proud..of you sushma 😘😘😘
For a video discussing a topic related to succinctly organizing ICH-GCP, the first two plus minutes feels as though our overloaded truck is about to tip over a cliff without warning. Review and edit. Try re-shooting. Voice each thought one time only. Move to next point.
This was my 1st video ever made on RUclips and 1st video of this channel.
Appreciate your suggestions will consider it and I hope the rest all videos on the channel you can see the improvement.
Can you describe simply by denoting giidline name and number along with 21 cfr, anvisa , ich, other guidelines. Means
Which guidelines refer to validation, qualification, investigation, risk assessment, change control, deviation, incidents, capa, root cause analysis, sampling techniques, manufacturing and packing, gdp, gmp. Etc
Plz awaited for response.
It will need whole RA departement of various fields to work on this thing, its a whole database you are asking.
very helpful thank you
V very nice
Thanks madam regarding to I am passed in nida tarining organisation but certificate not come😔💛💜
Very useful
Tq mam
Thanks
Nice
Did u say BUTTIFY?
Please clearly mention how can we help you, where you are getting problem?
what is the 4th principle
All available information should be adequate to support the proposed trial
Thnxs
Instead u have written in a paper
May I know what difficulty you are phasing.
Telugu lo cheppochu kada beauty
Very poor skills in teaching.... You confusing the viewers
It was my 1st video as student may be you liked new videos! Thank you for feedback.
Medam make a one vidio total ICH guidelines ?
same question Ma'm
didn't get your accent
Please read the subtitles!
Improve ut English first and then try to be clear
kindly make comparative video on ich vs usfda vs MHRA
better if with origin story of all
Ok, it will take a while but I will try....
But may I know what comparison u need because all 3 are totally different.
Us fda is regulatory agency of US whereas MHRA is for UK, ICH is not 1 particular Regulatory agency of a country.
What u want me to compare specify...