Webinar: "Defining DITA for Pharmaceutical Documentation"

DITA Pharmaceutical Content SC members:

OASIS is hosting a 30-minute webinar to educate potential 
participants on the proposed work of the DITA Pharma Subcommittee. Please plan 
to attend and help us promote the webinar by referencing it in your blogs or 
forwarding the invitation below to appropriate mailing lists and others who may 
be interested.

 

Thanks,

Carol

 

 

  
  

    
      

      
        
        

          
            
 

          
            
 

        

          
            

          
            
              
              

                
                  

              

                
                  
 

              

                
                  
Defining 
                  DITA for Pharmaceutical 
                  Documentation

              

                
                  
 

              

                
                  
                    
                    

                      
                        
                          
                          

                            
                              
Join 
                              us for a Webinar on September 
                              22

                          

                            
                              
 

                          

                            
                              

                          

                            
                              
 

                          

                            
                              
Space 
                              is limited.
Reserve 
                              your Webinar seat now at:
https://www1.gotomeeting.com/register/733810553

                          

                            
                              
 

                          

                            
                              
                                

                                
                                
Date: 
                                22 Sept 2009 
Time: 15:00 UTC (17:00 
                                Paris/11:00 Boston/8:00 San Francisco/23:00 
                                Beijing) 
                                

OASIS invites you to attend a free, 
                                30-minute webinar outlining the upcoming 
                                activities of the new DITA Pharmaceutical 
                                Content Subcommittee. The group is bringing 
                                together pharmaceutical documentation experts 
                                from all regions to define DITA topics and maps, 
                                as well as associated metadata and 
                                terminology.  The output of this 
                                Committee will address good practices as well as 
                                proposed DITA specialization; all stakeholders 
                                are strongly encouraged to be represented. 
                                

The webinar will provide examples of how 
                                the group’s recommendations may be used to 
                                streamline the creation of documentation 
                                supporting a product for scientific and 
                                regulatory purposes throughout its lifecycle. 
                                

While the actual scope and schedule will 
                                be determined by the Committee, some of the 
                                early topics may  include: 
- ICH 
                                Common Technical Document; 
- FDA Structured 
                                Product Labeling; 
- EU Product Information 
                                Management; and 
- Clinical Trial Protocol 
                                and Study Reports. 
   
Who 
                                should attend: 
Anyone with an interest in 
                                participating in or monitoring the work of the 
                                DITA Pharmaceutical Content Subcommittee 
                                including: 

* Medical and technical 
                                writers for pharmaceutical companies 
* 
                                Information technology architects with 
                                specialization in content and document 
                                management 
* Researchers who have expertise 
                                in the design of drug development programs, 
                                

Reference links: 

* DITA 
                                Pharmaceutical Content SC Statement of Work 
                                
http://lists.oasis-open.org/archives/dita/200905/pdf00000.pdf 
                                

* OASIS DITA Technical Committee 
                                
http://www.oasis-open.org/committees/dita/ 
                                

* OASIS Membership 
                                
http://www.oasis-open.org/join/categories.php

                                

                                
                                
 

                                

                                
                                
                                
                                

                                
                                
Title:

                                
                                
 

                                
                                
Defining 
                                DITA for Pharmaceutical 
                                Documentation

                                

                                
                                
 

                                
                                
 

                                
                                
 

                                

                                
                                
Date:

                                
                                
 

                                
                                
Tuesday, 
                                September 22, 
                                2009

                                

                                
                                
 

                                
                                
 

                                
                                
 

                                

                                
                                
Time:

                                
                                
 

                                
                                
11:00 
                                AM - 11:30 AM 
                                EDT

                                

                                

                                
                                
 

                                

                                
                                
After 
                                registering you will receive a confirmation 
                                email containing information about joining the 
                                Webinar.

                                

                                
                                
 

                              
 

                              
                                

                                
                                
System 
                                Requirements
PC-based 
                                attendees
Required: Windows® 2000, XP Home, 
                                XP Pro, 2003 Server, Vista

                                

                                
                                
 

                                

                                
                                
Macintosh®-based 
                                attendees
Required: Mac OS® X 10.4 (Tiger®) 
                                or newer

                                

                                
                                
 

                              

                        

                  

            

          
            

        

          
            
 

          
            
 

          
            
 

      

 

  
  

    
      

      
        
        

          
            
 

        

          
            
 

      

  

    
      
 

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