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Squib Documentation Release v0.14.0Andy MeneelyNov 11, 2017Contents12Install & Update 1.1 Prerequisites. . . 1.2 Typical Installation. . 1.3 Updating Squib. . 1.4 Specific Quirks. . . . . . . . .
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What is squib documentation?
Squib documentation is a set of official records and reports related to a specific medical product.
Who is required to file squib documentation?
Manufacturers, distributors, and marketers of medical products are required to file squib documentation.
How to fill out squib documentation?
Squib documentation can be filled out electronically or using paper forms provided by regulatory authorities.
What is the purpose of squib documentation?
The purpose of squib documentation is to track the safety and effectiveness of medical products in the market.
What information must be reported on squib documentation?
Squib documentation must include information such as adverse events, product defects, and changes in manufacturing processes.
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