Tuesday, August 14, 2007

About the Source Document

One of the oft used words in any clinical trial.The Source Document!
Helps track the conduct of any trial,leaves an audit trail to help reconstruct,evalute and hopefully also learn from all that happened during the trial.

This is what I'll try to do with this blog.
Pick up pieces from what is now the blazing trail of the clinical research industry in India.Where we shine,shimmer,or sometimes just gloss over.

The buzz about what the industry is,what it is great at and the paths it could explore. The story of the Research Industry ,so far and then go further!
Come walk with me and share your experiences,views,angsts ,hopes and I will share with you ,mine.

Be seeing you often!

Anupama

15 comments:

Unknown said...

Congratulations.It was time somebody started A blodg devoted to Clinical Trails.I am sure it will ahit and will disseminate valuable inforamtion.
Raju Parekh

Unknown said...

Congratulations.It was time somebody started A blog devoted to Clinical Trails.I am sure it will a hit and will disseminate valuable information.
Raju Parekh

Unknown said...

Good initiation and motivation for clinical research professionals!
This would be informative also. The experienced great professionals like you sharing the experiences and concepts would be worth for Clinical Research Industry.

Unknown said...

Good initiation and motivation for clinical research professionals!
This would be informative also. The experienced great professionals like you sharing the experiences and concepts would be worth for Clinical Research Industry.

Jayesh & Dilip

Unknown said...

Congratulations. Wonderful initiation from a well experianced and a great clinical research expert.I am sure it is going to be a continous knowledge sharing process.Looking forward......

Dr Gitanjali

Unknown said...

It is a great initiative by somebody who is one of the best in this field. Congratulation to Madam for her efforts & best of luck for her pathbreaking initiatves. It will be platform for all the clinical research professional to share their experience, query & encourage the creativity & sharing of knowledge.
I hope there will be more Deabates & Discussions which will help professionals to learn lot of things.

Hip Hip Hurray. Happy Independance Day to all & new movement in this field.

Vishal & Sita

Unknown said...

Cheers!! to 'THE SOURCE DOCUMENT'.
Indeed its a great initiative, now Clinical Research Industry can have a lot of informal interaction.
I hope CDM folkes will also find space here.
Kedar Deshmukh

swapna said...
This comment has been removed by the author.
Unknown said...

This is a wonderful initiation for the people who are the part of this science. By this way people may share their views among each other. I think the people who are working in this field, should have a minimum awareness in the regard of Ethics. This ethics should not come from guidelines but it must be come from the individual's heart. But now these days the commerce is more powerful than ethics.

Unknown said...

Congratulations. Its a graet instigation by the great mind.
I hope this will help us a lot to share our knowledges & experiences.
Thank you madam for your valuable efforts.

Debabrata

Anonymous said...

Thats great. Nice to hear experience people like you willing to share and educate professional in this field.

Best wishes to you as always......
kajal

Anonymous said...

Congratulations Madam.

This is a good initiation for to share a knowledge to everyone who has not much knowledge about the clinical research field. I hope that I am also getting good knowledge about other than my work.

Gaurang

sushil said...

FIRST OF ALL CONGRATULATION FOR THE GREAT INITIATION.
CAN WE PERFORM BA STUDIES UNDER ANDA KIND OF SCENARIO. FOR eg IF WE WANT TO TEST THE BIOAVILABILITY OF FIVE TEST FORMULATION (SINGLE PERIOD BA STUDY ON 30 VOL.)TO CHECK WHICH ONE IS GIVING BETTER PROFILE. SUSEQUENTLY THE BEST TWO WILL B PICKED UP FORCONDUCTING ROUTINE BE PILOT STUDY. WHAT IS THE RATIONALE OF THIS KIND OF STUDY. PROVIDE YOUR EXPERT COMMENT ON IT.

Anonymous said...

dear friends, as such, the concept of GCP is nebulous.and moreover when one goes through the ICH guidelines they appear as cold lifeless rules to be followed.one actually becomes GCP compliant and makes it a part of one's mental makeup only through experience and constant exposure to a GCP compliant environment.
can we think of any tools or methodologies(apart from one-day GCP workshops) wherein new inductees into the clinical research arena could imbibe the very spirit of GCP and get used to it so that it becomes a way of life(or way of work)to them?
waiting for innovative ideas from all of you.
Manjunath

Anonymous said...

Congratulations mam

This is really nice idea to share the knowledge and also getting the correct views from the knowlegable clinical professionals.

Anir Vora