Technical Report Writing
Customized Reports
Although we maintain standard report formats for all study types, Springborn will produce client-specific, customized study reports upon request. Many clients have their own internal electronic format requirements for templates, styles and fonts, and even client-specific organization of certain documents. In the spirit of partnership, we will customize study report formats to meet your specific documentation needs. Springborn recognizes the need to have a standardized format for a submission which may consist of studies crossing several disciplines. Contact us to discuss your custom formatting needs.
On Schedule
The commitment of our dedicated writing staff allows Springborn to accommodate your requirements for deadlines and submissions. We employ a staff of technical writers trained in incorporating laboratory study data into standardized report formats. Report writers possess a college degree in biology, chemistry, or an associated discipline and are responsible for producing reports for a variety of study types. All draft reports receive a full review by the Study Director prior to report audits performed by Springborn's Quality Assurance Unit. Draft reports are typically issued six to eight weeks following experimental termination (the last day of data collection). This period can be shortened considerably depending on your specific needs. Once you have reviewed the document you can communicate your draft report comments directly to the responsible Study Director and/or Technical Report Writer. In either case, the Study Director and Quality Assurance Group always fully review any changes in reports.
Standard Electronic Formats
Springborn prepares data and documents in the format you need for submission. Our standard report format is a Microsoft WORD document and an Adobe Acrobat .pdf file created from the native file which includes bookmarks and hyperlinks according to the formats suggested by EPA http://www.epa.gov/pesticides/regulating/registering/submissions/eproc-01-08-08.pdf,
OECD and FDA for electronic submissions. Whatever your electronic requirements Springborn has the resources and experience to get the job done.
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