(Q52011484)

English

An analysis of the SFSTP guide on validation of chromatographic bioanalytical methods: progress and limitations.

scientific article published in August 2003

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12899965

An analysis of the SFSTP guide on validation of chromatographic bioanalytical methods: progress and limitations. (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12899965

author name string

B Boulanger

1

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12899965

P Chiap

2

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12899965

W Dewe

3

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12899965

J Crommen

4

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12899965

Ph Hubert

5

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12899965

publication date

1 August 2003

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12899965

Journal of Pharmaceutical and Biomedical Analysis

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12899965

32

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12899965

4-5

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12899965

753-765

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12899965

Conceptual and statistical issues in the validation of analytic dilution assays for pharmaceutical applications.

1 reference

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An assessment of the 4-6-20 rule for acceptance of analytical runs in bioavailability, bioequivalence, and pharmacokinetic studies

1 reference

https://api.crossref.org/works/10.1016%2FS0731-7085%2803%2900182-1

7 January 2021

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A comparison of the Two One-Sided Tests Procedure and the Power Approach for assessing the equivalence of average bioavailability

1 reference

https://api.crossref.org/works/10.1016%2FS0731-7085%2803%2900182-1

7 January 2021

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An analysis of the Washington Conference Report on bioanalytical method validation.

1 reference

https://api.crossref.org/works/10.1016%2FS0731-7085%2803%2900182-1

7 January 2021

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An approximate distribution of estimates of variance components.

1 reference

https://api.crossref.org/works/10.1016%2FS0731-7085%2803%2900182-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0731-7085(03)00182-1

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12899965

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12899965

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