Updating international standards for pharmaceutical waters

17 Mar

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The USP is also available at pharmacy colleges, medical colleges, pharmaceutical manufacturers, equipment manufacturers, and some reference libraries.

These tests complemented other existing tests for particulates, micro-organisms, and endotoxins.

In some pharmacopoeia, tests for nitrate, nitrites, and other impurities were also required.

Jürgen Thürk, Convenor of the working group that developed the new standard.

Good Manufacturing Practices (GMP) relate to quality control and quality assurance enabling companies in the pharmaceutical sector to minimize or eliminate instances of contamination, mix-ups, and errors.

Anthony Bevilacqua, Director of R&D and Nick Dowd, Market Segment Manager Mettler-Toledo Thornton Historically, quality tests for bulk purified water (PW) and water for injection (WFI) were confined to the laboratory.It is advisable that the purchaser obtain this assurance.Source: The Ph RMA Water Quality Group These limits are Guidelines found in General Chapter by calling Customer Service at (800) 877-6733."The standard is of vital importance to the pharmaceutical industry and its suppliers of pharmaceutical primary packaging materials.For the first time, the principles of Good Manufacturing Practice are specified as part of an ISO standard," explained Dr.