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    <title>topic Re: SAS Clinical Data training in SAS Health and Life Sciences</title>
    <link>https://communities.sas.com/t5/SAS-Health-and-Life-Sciences/SAS-Clinical-Data-training/m-p/24083#M1033</link>
    <description>Hi,&lt;BR /&gt;
&lt;BR /&gt;
You may be interested in my new and unique class, Best Practices in SAS Statistical Programming for Regulatory Submission. It will be a two-day intense and comprehensive class in New Brunswick, New Jersey. During these two days, I expect to review all the details in the submission process and SAS macros for validating and producing publication-quality summary tables. I will also be available to answer any questions you may have.&lt;BR /&gt;
&lt;BR /&gt;
Best Practices in SAS Statistical Programming for Regulatory Submission&lt;BR /&gt;
- Download Class Outline and Brochure:&lt;BR /&gt;
[http://www.cfpa.com/PDF/2009/2234,C8-185,0903-409.pdf]&lt;BR /&gt;
- More update to date information on Class:&lt;BR /&gt;
[http://www.sascommunity.org/wiki/Best_Practices_in_SAS_Statistical_Program&lt;BR /&gt;
ming_for_Regulatory_Submission]&lt;BR /&gt;
&lt;BR /&gt;
- Best Practices in SAS Class Description:&lt;BR /&gt;
This course is intended for anyone directly or indirectly responsible for&lt;BR /&gt;
the creation, content or validation of summary tables, data lists and&lt;BR /&gt;
graphs used to support research, drug or medical device efficacy and&lt;BR /&gt;
safety in a regulatory submission. Professionals in the pharmaceutical,&lt;BR /&gt;
biotechnology and medical device industries who want to be 21 CFR Part 11&lt;BR /&gt;
compliant in relation to the SAS programming environment will benefit from&lt;BR /&gt;
this unique course. Effective and practical solutions to address real-&lt;BR /&gt;
world issues will be provided.&lt;BR /&gt;
&lt;BR /&gt;
This class is offered through The Center for Professional Advancement, an&lt;BR /&gt;
organization which is CEU accredited.&lt;BR /&gt;
&lt;BR /&gt;
&lt;BR /&gt;
Regards,&lt;BR /&gt;
Sunil</description>
    <pubDate>Thu, 02 Oct 2008 12:07:44 GMT</pubDate>
    <dc:creator>SunilGupta</dc:creator>
    <dc:date>2008-10-02T12:07:44Z</dc:date>
    <item>
      <title>SAS Clinical Data training</title>
      <link>https://communities.sas.com/t5/SAS-Health-and-Life-Sciences/SAS-Clinical-Data-training/m-p/24082#M1032</link>
      <description>Hi, I am SAS programmer working as an analyst in a Survey Research Industry, but now I want to learn about clinical data and looking to move towards Pharma Industry. Is there any training program for an individual with already a  SAS knowledge? If you can provide me with any guidance on available course, books, certifications etc.&lt;BR /&gt;
&lt;BR /&gt;
&lt;BR /&gt;
thank you.&lt;BR /&gt;
snk.</description>
      <pubDate>Mon, 09 Jun 2008 15:16:34 GMT</pubDate>
      <guid>https://communities.sas.com/t5/SAS-Health-and-Life-Sciences/SAS-Clinical-Data-training/m-p/24082#M1032</guid>
      <dc:creator>deleted_user</dc:creator>
      <dc:date>2008-06-09T15:16:34Z</dc:date>
    </item>
    <item>
      <title>Re: SAS Clinical Data training</title>
      <link>https://communities.sas.com/t5/SAS-Health-and-Life-Sciences/SAS-Clinical-Data-training/m-p/24083#M1033</link>
      <description>Hi,&lt;BR /&gt;
&lt;BR /&gt;
You may be interested in my new and unique class, Best Practices in SAS Statistical Programming for Regulatory Submission. It will be a two-day intense and comprehensive class in New Brunswick, New Jersey. During these two days, I expect to review all the details in the submission process and SAS macros for validating and producing publication-quality summary tables. I will also be available to answer any questions you may have.&lt;BR /&gt;
&lt;BR /&gt;
Best Practices in SAS Statistical Programming for Regulatory Submission&lt;BR /&gt;
- Download Class Outline and Brochure:&lt;BR /&gt;
[http://www.cfpa.com/PDF/2009/2234,C8-185,0903-409.pdf]&lt;BR /&gt;
- More update to date information on Class:&lt;BR /&gt;
[http://www.sascommunity.org/wiki/Best_Practices_in_SAS_Statistical_Program&lt;BR /&gt;
ming_for_Regulatory_Submission]&lt;BR /&gt;
&lt;BR /&gt;
- Best Practices in SAS Class Description:&lt;BR /&gt;
This course is intended for anyone directly or indirectly responsible for&lt;BR /&gt;
the creation, content or validation of summary tables, data lists and&lt;BR /&gt;
graphs used to support research, drug or medical device efficacy and&lt;BR /&gt;
safety in a regulatory submission. Professionals in the pharmaceutical,&lt;BR /&gt;
biotechnology and medical device industries who want to be 21 CFR Part 11&lt;BR /&gt;
compliant in relation to the SAS programming environment will benefit from&lt;BR /&gt;
this unique course. Effective and practical solutions to address real-&lt;BR /&gt;
world issues will be provided.&lt;BR /&gt;
&lt;BR /&gt;
This class is offered through The Center for Professional Advancement, an&lt;BR /&gt;
organization which is CEU accredited.&lt;BR /&gt;
&lt;BR /&gt;
&lt;BR /&gt;
Regards,&lt;BR /&gt;
Sunil</description>
      <pubDate>Thu, 02 Oct 2008 12:07:44 GMT</pubDate>
      <guid>https://communities.sas.com/t5/SAS-Health-and-Life-Sciences/SAS-Clinical-Data-training/m-p/24083#M1033</guid>
      <dc:creator>SunilGupta</dc:creator>
      <dc:date>2008-10-02T12:07:44Z</dc:date>
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