659 PACKAGING AND STORAGE REQUIREMENTS
Ancillary component:A component or entity that may come into contact with a Tertiary packaging component during the distribution, storage, and/or transportation of the packaged article (e.g., pallets, skids, and shrink wrap).
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1664 〉〉〉〉 ASSESSMENT OF DRUG PRODUCT …
latam-edu.usp.orgadministration ports, overwraps, adminstration accessories, labels, cardboard boxes, and shrink wrap. A Primary Packaging Component is in direct contact or may come into direct contact with the product (e.g., IV bag). A Secondary Packaging Component is in direct contact with a primary packaging component and may provide additional protection
USP <51> Antimicrobial Effectiveness Testing
latam-edu.usp.orgIf the diluted product exhibits antimicrobial properties, specific neutralizers may need to be incorporated into the diluents or the recovery media. The ability of the procedure to measure preservative efficacy may be compromised if the method suitability requires significant dilution (10 −2 or 10 −3) as this will affect the measured recovery
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1151 PHARMACEUTICAL DOSAGE FORMS
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Module 08 USP 1115 Bioburden Control of Non-Sterile …
latam-edu.usp.orgUnlike aseptic processing for which facility requirements are generally uniform in specification and performance, nonsterile product manufacturing environments typically involve diverse products and microbial contamination control requirements. In general, liquid, cream, or ointment products require a greater level of
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USP <71> Sterility Tests - United States Pharmacopeia
latam-edu.usp.orgThe view from USP <1211> Sterilization and Sterility Assurance of Compendial Articles : 6 ... For products containing a mercurial preservative that cannot be tested by the ... Used for sterility testing of viscous products and for devices having tubes with small lumen.
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1117 MICROBIOLOGICAL BEST LABORATORY PRACTICES
latam-edu.usp.orgWhenever possible, sampling equipment should be loaded with its microbiological recovery media in the environment that is to be sampled. All testing in laboratories used for critical testing procedures, such as sterility testing of final dosage forms, bulk product, seed
71 〉〉〉〉 STERILITY TESTS
latam-edu.usp.orgof the test. Modify the conditions in order to eliminate the antimicrobial activity, and repeat the Method Suitability Test. This method suitability is performed (a) when the test for sterility has to be carried out on a new product; and (b) whenever there is a change in the experimental conditions of the test.
1092 THE DISSOLUTION PROCEDURE: DEVELOPMENT AND …
latam-edu.usp.org5.4 Precision 5.4.1 Repeatability of Analysis 5.4.2 Intermediate Precision/Ruggedness 5.4.3 Reproducibility 5.5 Robustness 5.6 Stability of Standard and Sample Solutions ... (such as dynamic solubility, potentiometric titration, or turbidity measurement methods). (USP …
STERILIZATION OF COMPENDIAL ARTICLES
latam-edu.usp.orgFor steam and dry heat, the D-value is a function of temperature. In gas sterilization (ethylene oxide, ClO , or O ), D-values are a function of the chemical concentration, relative humidity, and temperature. Similarly, for liquid chemical sterilization the D-value is a function of the temperature and sterilant concentration.
660 〉〉 CONTAINERS—GLASS
latam-edu.usp.orgglass containers will raise the hydrolytic resistance from a moderate to a high level, changing the classification of the glass to Type II. The following recommendations can be made as to the suitability of the glass type for containers for pharmaceutical products, based on the tests for hydrolytic resistance.
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<659> Packaging and Storage Requirements Type of Posting
www.uspnf.comá659ñ PACKAGING AND STORAGE REQUIREMENTS Change to read: (A portion of the Associated Components section of this chapter will become official on May 1, 2019, and a portion of the Packaging section of this chapter will become official on May 1, 2020, as indicated. Early adoption of the require-ments in this chapter and Plastic Materials of Construction á661.1ñ and …
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www.uspnf.com1 〈659〉 PACKAGING AND STORAGE REQUIREMENTS 2 Change to read: 3 (A portion of the Associated Components section of this chapter will 4 become official on May 1, 2019, and a portion of the Packaging 5 section of this chapter will become official on May 1, 2020, December 1, 2025 6 (USP 1-Aug-2020) as indicated. Early adoption of 7 the requirements in this chapter …
Other transportation-related fees and shipping information 1
www.fedex.com7) is encased in an outer shipping container covered in shrink wrap or stretch wrap; 8) is encased in a soft-sided pack (e.g., courier packs, poly bags and bubble mailers) that exceeds 18 inches along its longest side or 13 inches along its second-longest side or 5 inches in height;