PHARMACY

Dispensing and Weighing Controls

Aug 21, 2016 by in PHARMACY Comments Off on Dispensing and Weighing Controls

!DOCTYPE html PUBLIC “-//W3C//DTD XHTML 1.1//EN” “http://www.w3.org/TR/xhtml11/DTD/xhtml11.dtd”> Chapter 45: Dispensing and Weighing Controls Dispensing and weighing controls should be such that the identity, purity, and quality of the raw materials…

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In-Process Controls

Aug 21, 2016 by in PHARMACY Comments Off on In-Process Controls

!DOCTYPE html PUBLIC “-//W3C//DTD XHTML 1.1//EN” “http://www.w3.org/TR/xhtml11/DTD/xhtml11.dtd”> Chapter 44: In-Process Controls 21 CFR 211.110 and Eudralex Volume 4 21 CFR 211.110 “Sampling and Testing of In-process Materials and Drug Products”;…

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Stability Programs

Aug 21, 2016 by in PHARMACY Comments Off on Stability Programs

  Commercial Support Stability As part of the submission process, a company will include a commitment to continue stability evaluation over the commercial life of the product. The stability commitment…

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Compendia (US, Europe, and Japan)

Aug 21, 2016 by in PHARMACY Comments Off on Compendia (US, Europe, and Japan)

  Though not a compendial specification, the PhEur suggests a total aerobic microbial count (TAMC) action limit of 10 CFU/100 mL in its WFI monograph, which agrees with the 1993…

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Production Operations

Aug 21, 2016 by in PHARMACY Comments Off on Production Operations

  Sanitization and Hygiene Clean areas should be cleaned thoroughly according to documented procedures. Detailed hygiene programs should be established. They should include procedures relating to the health, hygiene practices,…

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Laboratory Investigations of Aberrant Results

Aug 21, 2016 by in PHARMACY Comments Off on Laboratory Investigations of Aberrant Results

  The principles of conducting an analytical OOS investigation heretofore described should be invoked throughout an MDD investigation, including proper documentation, collection of data, and interpretation of data by the…

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Salvaged/Returned Goods and Destruction

Aug 21, 2016 by in PHARMACY Comments Off on Salvaged/Returned Goods and Destruction

!DOCTYPE html PUBLIC “-//W3C//DTD XHTML 1.1//EN” “http://www.w3.org/TR/xhtml11/DTD/xhtml11.dtd”> Chapter 41: Salvaged/Returned Goods and Destruction Good manufacturing practices (GMP) regulations were designed to ensure that pharmaceutical products that are manufactured and released…

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Master Batch and Completed Batch Records

Aug 21, 2016 by in PHARMACY Comments Off on Master Batch and Completed Batch Records

!DOCTYPE html PUBLIC “-//W3C//DTD XHTML 1.1//EN” “http://www.w3.org/TR/xhtml11/DTD/xhtml11.dtd”> Chapter 42: Master Batch and Completed Batch Records Clearly written, detailed batch records are critical to ensuring product quality. The master batch record…

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Shipping and Distribution

Aug 21, 2016 by in PHARMACY Comments Off on Shipping and Distribution

!DOCTYPE html PUBLIC “-//W3C//DTD XHTML 1.1//EN” “http://www.w3.org/TR/xhtml11/DTD/xhtml11.dtd”> Chapter 39: Shipping and Distribution A finished pharmaceutical’s labeling and/or pharmacopeia monograph provide specific directions for the temperature and humidity conditions of storage…

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