Our process for developing your
CD-ROM is designed to be low impact to your already hectic schedule.

1. We can leverage your existing investigator meeting content, if available, such as PowerPoint™ presentations, web cast content, audio or video tapes
   
   
2. You are the experts. We go to the source for the audio scripts, either culling the content from your speaker notes or recording the presenter to capture all of the detail points to be communicated.
   
   
3. We edit these transcripts for brevity and succinctness, paying close attention to not inadvertently change the intended message. Our goal is to provide the user with as much content as they can handle in as little time as possible.
   
   
4. We follow the familiar agenda of a typical investigator meeting. The content is organized so that study staff can find the information that is appropriate to their tasks.
   
   
5. You have input and review opportunities at predefined milestones throughout the development process.
   
   
6. We provide you an easy to manage paper based document to confirm content and to make alterations as appropriate. All content is tagged with a predefined numbering/tracking convention so confirming revisions is streamlined.
   
   
7. Your approved scripts are then recorded by professional voice talent with experience reading medical copy. All this is done in a professional recording studio to obtain the highest quality voiceover for your production. A member of your clinical team is required to be present to confirm the accuracy of the content and to monitor pronunciation as the script is being read.
   
   
8. Most of our production activities happen concurrently to help constrain the production timeline to 8-10 weeks. Should your production require instances of new animation or video to communicate a complex concept or illustrate a series of activities we will attempt to anticipate & accommodate this in the production timeline.