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of homeopathic drug products Correspondences to regulation 211167 stating the requirements for sterility testing are covered in Sections 1 4 of the interpretation of regulation C02029 (Sterile Products) The Canadian GMP code does not have any guidance covering the testing of ophthalmic ointments and controlled-release dosage forms Correspondences to regulation 211170 stating the requirements for reserve samples are covered in Section 1 of regulation C02025 and in regulation C02026 and Sections 1 and 3 5 of their interpretation Correspondences to regulation 211173 stating the requirements for laboratory animals are covered in Section 24 of the interpretation of regulation C02004 The Canadian GMP code does not have correspondence to regulation 211176, which covers the requirements for the testing and handling of penicillin contamination.

The letters are written in flowery, rather pretentious language that appeals equally to your greed and vanity People fall for this Horrifyingly enough, people die for this; at least we presume so, as they go to Nigeria (or whatever country) to claim their funds, and never return Others make a hobby of replying to the scammers and stringing them along in return Some have even managed to get the scammers to give them money Scambaiting, as it s called, is amusing and probably not dangerous, but I recommend against cashing any checks you may receive Any time someone important in a third-world country dies, Nigerian letters begin making the rounds Within a day of Yasir Arafat s death, letters claiming to be from his wife, Suha, began arriving in people s inboxes Is this phishing By my definition, yes.

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Correspondences in EU GMP Code In the EU GMP code [15] issues related to laboratory controls are covered in s 1 (Quality Management), 4 (Documentation), 5 (Production), and 6 (Quality Control) and in Annexes 1 (Manufacture of Sterile Medicinal Products), 9 (Manufacture of Liquids, Creams, and Ointments), and 19 (Reference and Retention Samples) Correspondences to regulation 211160 are covered in Subchapters 14, 42, 43, 410 413, 515, 67, and 618, which cover the general requirements for laboratory controls Correspondences to regulation 211165 are covered in Subchapters 422, 423, 561, 562, 63, 611, and 615, which state the requirements for the release for distribution, the testing of nished drug products, and the handling of rejected drug products The EU GMP code does not have correspondence to regulation 211.

Different approaches are discussed for establishing traceability and assessing MU of analytical methods in general The importance of both concepts and the link with method validation and analytical quality assurance are highlighted 823 8231 METHOD VALIDATION AND QUALITY ASSURANCE Role of Method Validation in AQA.

166, which states the requirements for stability testing However, there is a separate guideline, Stability Testing on Active Ingredients and Finished Products [59], which provides guidance on issues related to stability testing Furthermore, Subchapters 623 633 cover the requirements for the on-going stability program Correspondences to regulation 211167 are covered in Annexes 1 and 9 Section 93 of Annex 1 covers the requirements for sterility testing and Annex 9 the requirements for ointments In the EU GMP code there is no guidance on the testing of the controlled-release dosage forms Correspondences to regulation 211170 are covered in Subchapters 14 and 612 and Annex 19, which state the requirements for reserve samples Correspondences to regulation 211173 are covered in Subchapters 333 and 622, which state the requirements for the maintenance of animals.

Because it s so old, however, it s not something I m going to concentrate on in this book If something is too good to be true, it probably is..

The EU GMP code does not have correspondence to regulation 211176, which covers the requirements for the testing and handling of penicillin contaminations Correspondences in WHO GMP Guideline In the WHO GMP guideline [36] issues related to laboratory controls are covered in s 14 (Materials), 15 (Documentation), 16 (Good Practices in Production), and 17 (Good Practices in Quality Control) Correspondences to regulation 211160 are covered in Subchapters 1514 1516, 1518 1521, 163, and 1623, which state the general requirements for laboratory controls Correspondences to regulation 211165 are covered in Subchapters 1428, 1429, 1513, 1542, 177 1713, 1719, and 1720, which state the requirements for the release for distribution covering the testing of nished drug products and the handling of rejected drug products Correspondences to regulation 211166 are covered in Subchapters 17.

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