Description
Summary:
Provides researchers, clinicians and general requests with scientific reprints describing work that has been performed using clinical devices and research systems. Intended to ensure that company reprints are appropriately distributed and that company does not promote an unapproved product or unapproved uses. Laboratory use only systems are not governed under the same restrictions, but will be maintained in a similar manner. Applies to all related reprints controlled and distributed from the US only. Does not apply to non-scientific materials (e.g., investor relations material), or European distribution of reprints. Covers article manuscript submission, library maintenance, review and maintenance of library, reprint request, reprint fulfillment, and archiving.
Included Sections:
Purpose, Scope, Responsibility, References and Applicable Documents, Materials and Equipment, Health and Safety Considerations, Documentation Requirements, and Procedures
Included Attachments/Appendices:
Medical Inquiry Form, Article Submission Form, Reprint Fulfillment Form Letter
About This Document:
This is not a generic template, it's a 6-page procedure that was actually created and used in the Sales & Marketing operations of a FDA-regulated establishment. The company-specific information (names, addresses, some images, proprietary product information, etc.) has been redacted but the content and format have been largely preserved.
Reasons to Buy:
- Use it as a starting point for your own documentation project
- Compare the quality of your documents against your industry peers
- Learn what other companies in your industry are actually doing
Who Will Benefit:
- Sales & Marketing Managers
- Regulatory Affairs Managers
- Executive Management
Product Details
- Edition:
- 1.0
- Published:
- 08/01/2007
- Number of Pages:
- 6
- File Size:
- 1 file , 410 KB
