PharmPK Discussion - Bioavailability study protocols

• On 25 Nov 1996 at 10:08:28, mzhuk.aaa.paco.net sent the message
  

  
  I would like to know about investigation of bioequivalent drugs (standard
  protocols). Please let me know.
  
  Thanks for your help
  
  Olga Zhuk, Ph.D.
  
  

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• On 26 Nov 1996 at 13:10:40, DGarg8838.aaa.aol.com sent the message
  

  
  I do not understand this message. We conduct many bioavailability studies and
  have experience in the development of standard protocols. We also write
  reports for bioavailability studies. If you need help in writing a chapter
  for a text book, we may be able to assist you. Please clarify your message
  and let us know if we can assist you in any way.
  
  Dyal Garg, Ph.D.
  Clinical Research Services, Inc.
  8838 Indian River Run
  Boynton Beach, FL 33437
  Phone: 561-737-3954
  Fax: 561-732-1941
  E-Mail:DGarg8838.at.aol.com
  
  

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• On 26 Nov 1996 at 13:29:27, "David S. Farrier" (dfarrier.at.bright.net) sent the message
  

  
  Olga,
  
  You will find a direct link to the full text of FDA/CVM's 1996
  Bioequivalence Guidelines in the Regulations and Guidelines portion of my
  Link page on my web site (Yes! This is advertising. Why else would I put
  such useful stuff there?) at http://www.bright.net/~dfarrier/index.html
  
  David
  
  Dr. David S. Farrier
  Summit Research Services
  1374 Hillcrest Drive
  Ashland, OH 44805 USA
  (419)-289-9207
  E-mail: dfarrier.-at-.bright.ne
  Internet:  http://www.bright.net/~dfarrier/index.html
  
  [David I hope you don't mind...but the link above is on the page
  http://www.bright.net/~dfarrier/links/links.htm in the Regulations and
  Guidelines portion. The link from home page above to this page is called
  Links. ;-) DB]
  
  

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