Podcast
Questions and Answers
Why is programmatic access to FederalRegister.gov and eCFR.gov limited?
Why is programmatic access to FederalRegister.gov and eCFR.gov limited?
What do you need to complete to request access to FederalRegister.gov and eCFR.gov?
What do you need to complete to request access to FederalRegister.gov and eCFR.gov?
How long is a request for access to FederalRegister.gov and eCFR.gov valid for?
How long is a request for access to FederalRegister.gov and eCFR.gov valid for?
What should you do if you want to request a wider IP range?
What should you do if you want to request a wider IP range?
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What type of website is FederalRegister.gov?
What type of website is FederalRegister.gov?
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What is the primary purpose of analytical method validation?
What is the primary purpose of analytical method validation?
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What information must be included on a sample label?
What information must be included on a sample label?
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What type of records must be maintained in a laboratory?
What type of records must be maintained in a laboratory?
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Why is it essential to handle and transfer samples properly?
Why is it essential to handle and transfer samples properly?
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How long must laboratory records be retained?
How long must laboratory records be retained?
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Study Notes
Access to FederalRegister.gov and eCFR.gov
- FederalRegister.gov and eCFR.gov limit programmatic access due to aggressive automated scraping.
- Human users can request access by completing a CAPTCHA (bot test) to add their IP address to the allowed list.
- Access requests are valid for approximately three months before needing to be repeated.
Wider IP Range Requests
- To request access for a wider IP range, first request access for the current IP address.
- Then, use the "Site Feedback" button (found in the lower left-hand side) to make the request.
Laboratory Procedures
- Testing and analysis must adhere to established procedures and protocols to ensure accuracy and reliability
Laboratory Equipment Management
- Laboratory equipment must be properly installed, operated, and maintained to prevent errors and contamination
- Equipment calibration and standardization records must be maintained, including date, time, and results
- Equipment must be cleaned, sanitized, and labeled regularly to prevent contamination and ensure traceability
Analytical Method Validation
- Analytical methods must be validated to ensure accuracy, precision, and reliability
- Validation involves assessing specificity, linearity, range, accuracy, precision, detection limit, and quantitation limit
- Validation records must include method description, validation protocol, results, date, and time of validation
Sample Handling and Identification
- Samples must be properly identified and labeled to ensure traceability, including sample identifier, description, date, and time of sampling
- Samples must be stored to prevent contamination, degradation, or loss
- Samples must be handled and transferred to prevent mix-ups or contamination
Documentation and Record Keeping
- Laboratory records must include test and analysis results, calibration and standardization records, analytical method validation records, and sample identification and storage records
- Records must be accurate, complete, legible, and retained for a specified period of time
- Records must be accessible and available for review during inspections and audits
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Description
Learn about the rules and procedures for accessing FederalRegister.gov and eCFR.gov, including how to request access and manage IP addresses.