Model-Integrated Bioequivalence (MIBE) in Generic Drug Research: Can We Ease the Bioequivalence Burden? [PDF]
Kollipara S +3 more
europepmc +1 more source
Phase I Study Evaluating Pharmacokinetics, Pharmacodynamics, Safety, and Immunogenicity of Recombinant Human Serum Albumin (rHSA) in Healthy Adults. [PDF]
Panuganti VK +9 more
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Active-controlled commercial field evaluation of an independently developed fluralaner oral solution for poultry red mite control in laying hens. [PDF]
Liu Z +8 more
europepmc +1 more source
Guiding a Diclofenac Sodium Dual-Release Sustained Formulation Development Through In Vitro-In Vivo Relationship Based on Physiologically Based Pharmacokinetics. [PDF]
Wang Q +7 more
europepmc +1 more source
Short-Term HbA1c Non-Inferiority of Synthetic Semaglutide Should Not Be Conflated With Full Therapeutic Interchangeability. [PDF]
Singh AK, Singh A, Singh R.
europepmc +1 more source
Foreign Comparator Drug Products, Manufacturing & Supply Chain Considerations for Otic, Ophthalmic, And Parenteral Solutions - Generic Drugs Perspective. [PDF]
Nana A +4 more
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A randomized, open, two-period, cross-over, single oral dose, pharmacokinetics and bioequivalence study of vitamin K<sub>1</sub> in healthy volunteers under fasting and fed conditions. [PDF]
Li Y +5 more
europepmc +1 more source
Reply: Methodological considerations in the ADAPT-1 ovarian stimulation study. [PDF]
Bernabeu A +7 more
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Comment on 'Real-World Evidence of the Effectiveness and Safety of Biosynthetic Semaglutide in Type 2 Diabetes: A Multicentre Study From Pakistan'. [PDF]
Shahid F, Khan MF.
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A Novel Ultra-Performance Liquid Chromatography-Electrospray Ionisation-Tandem Mass Spectrometry Method for Quantification of Imeglimin in Human Plasma: Application to a Bioequivalence Study. [PDF]
Wadie M +5 more
europepmc +1 more source

