E Learning Regulatory History Document

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Project Main Details

E Learning Regulatory History Document 
Casual, yet professional style voice over for a training course No "broadcaster or announcer voice". Please talk like you are an employee. Must be available to do retakes on short notice with a 12 hour turn around.

Recording will be this week/early next week. Final .wav files due by Tuesday 3/25. Please note any additional charges should a re-record be needed for a couple of screens.

Person hired will be required to submit a tax ID and sign a confidentiality agreement prior to starting the work to get paid. Also, after the invoice is sent to us, it takes approximately 45 days for payment to be processed.

~12 Screens of content ~ 10-12 minutes. Each screen will need to be its own .WAV file.

FDA-say letters F-D-A
RHD-say letters R-H-D
FDA OPDP-two words say letters, F-D-A O-P-D-P
FDA USPI-two words say letters, F-D-A U-S-P-I
RACM--say "rack-um" 
2014-03-17 16:14:47 GMT
2014-03-19 17:00:00 (GMT -05:00) Eastern Time (US & Canada) 
Yes (click here to learn more about Voice123's SmartCast)
0 direct invitation(s) have been sent by the voice seeker resulting in 0 audition(s) and/or proposal(s) so far.
Voice123 SmartCast is seeking 25 auditions and/or proposals for this project (approx.) Invitations sent by SmartCast have resulted in 25 audition(s) and/or proposal(s) so far.

Project Parameters

The Voice Actor should be located in:
Fixed - USD 550
Training, business presentations, sales, and web sites
15 Minutes
English - USA and Canada
Middle Age Female OR Middle Age Male
• Audio files must be delivered via email
• Deliver edited and finished voice tracks AND
• Provide voice direction
Not defined
The voice seeker is willing to hire either union or non-union talents for this project

Script Details

custom demo required 
The RHD is regularly modified and updated.
Regulatory Affairs is responsible for the creation, content review, approval and maintenance of Regulatory History Documents. Every year, the content of each RHD is reviewed and updated, if required. However, there are some events which may trigger a review and update sooner than the annual review.
Those include receipt of:
- FDA OPDP advisory or correspondence
- FDA USPI labeling supplement approval, where the labeling supplement approval significantly impacts the RHD (such as a new or modified indication, patient, population, dosage form)
- or FDA OPDP enforcement actions (such as Untitled or Warning Letters) for the product 
Please note that you should only use the script or your recording of it for auditioning purposes. The script is property, unless otherwise specified, of the voice seeker and it is protected by international copyright laws.

Voice-Seeker Details

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