Jump to content

Indian Pharma Law - Is this true?


summer27

Recommended Posts

21 minutes ago, Spartan said:

dani generic version create chesademo

Insulin is one of the preserved drug made by. India ... and that too killed by foreign company... because of our politicians... 

 

Thanks to the founder and CEO.. who is a Telugu guy.. 

 

 

Link to comment
Share on other sites

12 minutes ago, Kootami said:

They do it after patent ends

no..what she is saying is if the cost of the drug is not affordable, then they give patents to local company..

Link to comment
Share on other sites

True.. cheap labour.. acquring raw api from europe illegally

workers get peanut salaries compared to west.

pharm qa associate: 15000 rs/ month( its $ 70000 / year in usa )

pharmacist : 18000rs/ month( 100000$/ year in usa)

Link to comment
Share on other sites

Just now, Midnightsun said:

True.. cheap labour.. acquring raw api from europe illegally

workers get peanut salaries compared to west.

Yes, max 5000 workers get peanut salaries. But also,  1.5 billion people get cheaper drugs..

  • Upvote 1
Link to comment
Share on other sites

1 hour ago, pizzaaddict said:

One Downside of these sort of  manufacturing is quality Ani @JackSeal opinion. 

Bayya, FDA quality inspections untayi..If they find any issues they put warning letters and will not approve the drugs if they want to market in USA

Link to comment
Share on other sites

1 hour ago, summer27 said:

 

em madluthundi bhayya...patented drug in western countries valla drug composition ela dorukuthadi ivvaniki... avem Indialo register ayyi leve.. any patented drug will get an exclusivity only for 15 years after they invent the drug. After that any company file and create the generic version of that drug. adi ye country ayina chestadi..not only India. 90% of the generic drugs in USA are produced from China(40%), Mexico (35) and India (25%).

Link to comment
Share on other sites

India does not recognize patents to end products when it comes to pharma. The patent is only for process. So you can minutely change the process and create almost same product - legally.

 

Link to comment
Share on other sites

4 hours ago, MaZA said:

Bayya, FDA quality inspections untayi..If they find any issues they put warning letters and will not approve the drugs if they want to market in USA

FDA only for USA markets and Indian markets lo release chesey some medicines have issue . Not all of them and few of them .

Link to comment
Share on other sites

Join the conversation

You can post now and register later. If you have an account, sign in now to post with your account.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

×
×
  • Create New...