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Search for "bioequivalence"

Displaying results 1 to 3 out of 3

  Trial Expertise 81%
  ... modes of administration such as oral, transdermal, buccal and sublingual. In 2008, 2009, 2010, 2011 and 2014, the FDA performed inspections of bioequivalence studies and awarded the highest rating in all cases: ‘No Action Indicated’. Food-drug interaction Although in most trials a standard high-fat ... CRS has extensive knowledge in the field of skin-related investigative and safety measurements, the development of TTS/TDS, bioavailability and
  Size: 34 K - Created: 18-11-12 - Modified: 02-08-19 10:27
Path: /Expertise/Trial Expertise

  2000 – 2009 66%
  ... What is the "optimal" follow-up schedule for ICD patients? Europace. 2005 Jul; 7(4):319-26. Stahlberg HJ, Beier H, Baumann-Noss S , Birkel M. Bioequivalence of a new clarithromycin 250 mg dst (dose sipping technology) granule formulation (clarosip®) compared to an equimolar reference suspension ... 1053-62. Grossmann M, Ebert U, Baumann- Noss S , Birkel M, Renner J, Luecker PW. An approach to characterize pharmacokinetic – pharmacodynamic
  Size: 53 K - Created: 09-11-15 - Modified: 02-08-19 10:27
Path: /Expertise/Published Expertise/2000 – 2009

  2010-2020 61%
  ... May 20. doi: 10.1111/bcp.14389. [Epub ahead of print] Grill S, Bruderer S, Sidharta PN, Antonova M, Globig S, Carlson J, Schultz A , Csonka D. Bioequivalence of macitentan and tadalafil given as fixed-dose combination or single-component tablets in healthy subjects. Br J Clin Pharmacol 2020 May 6. ... J Clin Pharmacol. 2012 Nov 28. [Epub ahead of print] Cawello W, Bökens H, Nickel B, Andreas JO, Halabi A . Tolerability, pharmacokinetics, and
  Size: 71 K - Created: 09-11-15 - Modified: 08-07-20 10:17
Path: /Expertise/Published Expertise/2010-2020