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Part 211--Current Good Manufacturing Practice for Finished Pharmaceuticals

Subpart J--Records and Reports
Sec. 211.182 Equipment cleaning and use log.

TITLE 21--FOOD AND DRUGS

CHAPTER I--FOOD AND DRUG ADMINISTRATION
DEPARTMENT OF HEALTH AND HUMAN SERVICES

PART 211--CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS

Subpart J--Records and Reports

Sec. 211.182 Equipment cleaning and use log.

A written record of major equipment cleaning, maintenance (except routine maintenance such as lubrication and adjustments), and use shall be included in individual equipment logs that show the date, time, product, and lot number of each batch processed. If equipment is dedicated to manufacture of one product, then individual equipment logs are not required, provided that lots or batches of such product follow in numerical order and are manufactured in numerical sequence. In cases where dedicated equipment is employed, the records of cleaning, maintenance, and use shall be part of the batch record. The persons performing and double-checking the cleaning and maintenance shall date and sign or initial the log indicating that the work was performed. Entries in the log shall be in chronological order.


Equipment Log Books

Laboratory Equipment Log Book

  • Pages are Individually Numbered and include a Log Book number field
  • Column headings are Date, Activity Performed/Observations/Notes, Signature
  • Guidelines page includes FDA Sec. 211.182 Equipment cleaning and Use Log rules
  • Hardbound Book with Sewn Pages and Round Spine
  • 24lb. Acid-Free Archival-Safe Paper
  • Red Imitation Leather Cover
  • Available in two sizes:
    - Small 8" X 10" (20.3cm X 25.4cm) or
    - Large 8-7/8" X 11-1/4" (22.5cm X 28.6cm )
  • 96 pages
  • Usually ships out within 24 hours
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