Monday, February 10, 2014

Sending emails through SAS

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I am not sure if there is any practical use for sending emails through SAS. But this SAS micro was picked up from RTP SAS User Group Email...
3 comments:
Sunday, February 02, 2014

Conference in Research Triangle Park, NC: TRENDS AND INNOVATIONS IN CLINICAL TRIAL STATISTICS (2014)

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The research triangle area in North Carolina is one of the area with the concentrated talents in statistics and biostatistics. All three bi...
1 comment:
Sunday, January 26, 2014

FDA Guidance Webinar Series

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FDA's Guidance Webinar series aims to foster collaboration and transparency in the development of guidance documents through direct ou...

Overrunning Issue In Adaptive Design Clinical Trials

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Adaptive designs have been more and more commonly used from early phase clinical trials to late phase pivotal clinical trials and from the ...
Friday, January 24, 2014

Archives of Webcast and Presentation Slides for Public Workshop on Complex Issues in Developing Drug and Biological Products for Rare Diseases

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To meet the requirements by PDUFA V  and FDASIA , FDA organized a public workshop on "Complex Issues in Developing Drug and Biological ...

Free Webinar by FDA on the final guidance for industry Electronic Source Data in Clinical Investigations

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On Wednesday, January 29, 2014, from 2:00PM - 3:00PM EST, FDA will present a webinar on the final guidance for industry Electronic Source Da...
Wednesday, January 01, 2014

Artistic and Creative Way in Naming a New Drug

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We all may have difficulties in remembering the drug names and wonder why many drug names are so awkward and difficult to read. For drug ma...
Thursday, December 26, 2013

Quantification of Risk – Breaking down adverse reaction into common and uncommon categories

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When we conduct a clinical trial using an approved product, we may run into the requests for the list of common, very common adverse events...
Tuesday, December 10, 2013

Pharmacokinetic studies when endogenous compounds exist and pre-dose concentrations are not zero

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This Monday, FDA issued a new guidance titled “ Bioequivalence Studies with Pharmacokinetic Endpoints for Drugs Submitted Under an ANDA ”. ...
9 comments:
Sunday, December 08, 2013

SAS Programming for PK Time-Concentration Curve Using SGPLOT

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Comparing with other software/tools for generating the graphs, SAS/Graph may be inferior. Programming to generate graphs using SAS/Graph la...
2 comments:
Sunday, November 17, 2013

Causality Assessment, Causality Categories for Reporting Adverse Events or Adverse Reactions

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In clinical trials, safety reporting is a critical issue. This includes the reporting of safety information (adverse events or adverse reac...