PubMed ID: 7867670Using in vitro dissolution and in vivo absorption of different generics or batches for an appropriate drug and dosage form, a reference equation of form: {Mathematical expression} can be proposed. In the case of availability of standardised in vitro-in vivo data for a specific drug, a Level A a correlation of this type containing experimentally determined a, b, d parameters would serve to predict in vivo absorption phase of the drug. The larger number of batches, the stronger will be the predictive power of these parameters. © 1994 Springer-Verlag
In the development of new oral drug compounds, poorly water-soluble compounds are a challenge for th...
In vitro dissolution has been recognized as an important element in drug development to assure the q...
none7noWith the aim of developing an in vitro model for the bioavailability (BA) prediction of drugs...
A biopharmaceutics drug classification scheme for correlating in vitro drug product dissolution and ...
In vitro drug dissolution-time profiles can be used to predict in vivo drug plasma concentration-tim...
A computer method and software based on the in vitro dissolution ofdrug preparations has been elabor...
In vivo bioavailability studies are performed for new drug to establish essential pharmacokinetic pa...
A generic drug product (test product) is bioequivalent to an innovator product (reference product) w...
A computer method and software based on the in vitro dissolution ofdrug preparations has been elabor...
A computer method and software based on the in vitro dissolution ofdrug preparations has been elabor...
In vitro dissolution has been extensively used as a quality control tool for solid oral dosage forms...
In bioequivalence assessment, pharmacokinetic characteristics of concentration-time curves have trad...
For approval of generic drugs, the FDA requires that evidence of bioequivalence in average bioequiva...
ABSTRACT To improve the quality of pharmaceutical products in their markets, several Latin American ...
In order to assess and predict the bioequivalence (BE) of oral drug products, a new in vitro system ...
In the development of new oral drug compounds, poorly water-soluble compounds are a challenge for th...
In vitro dissolution has been recognized as an important element in drug development to assure the q...
none7noWith the aim of developing an in vitro model for the bioavailability (BA) prediction of drugs...
A biopharmaceutics drug classification scheme for correlating in vitro drug product dissolution and ...
In vitro drug dissolution-time profiles can be used to predict in vivo drug plasma concentration-tim...
A computer method and software based on the in vitro dissolution ofdrug preparations has been elabor...
In vivo bioavailability studies are performed for new drug to establish essential pharmacokinetic pa...
A generic drug product (test product) is bioequivalent to an innovator product (reference product) w...
A computer method and software based on the in vitro dissolution ofdrug preparations has been elabor...
A computer method and software based on the in vitro dissolution ofdrug preparations has been elabor...
In vitro dissolution has been extensively used as a quality control tool for solid oral dosage forms...
In bioequivalence assessment, pharmacokinetic characteristics of concentration-time curves have trad...
For approval of generic drugs, the FDA requires that evidence of bioequivalence in average bioequiva...
ABSTRACT To improve the quality of pharmaceutical products in their markets, several Latin American ...
In order to assess and predict the bioequivalence (BE) of oral drug products, a new in vitro system ...
In the development of new oral drug compounds, poorly water-soluble compounds are a challenge for th...
In vitro dissolution has been recognized as an important element in drug development to assure the q...
none7noWith the aim of developing an in vitro model for the bioavailability (BA) prediction of drugs...