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Books by Rebecca Mashaw

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13 books found
European authorities opted to apply ICH broadly.(USP/PDA Conference): An article from: Validation Times
European authorities opted to apply ICH broadly.(USP/PDA Co…
By: Rebecca Mashaw
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Speakers suggest strategies to meet new USP residual solvent requirements.(USP/PDA Conference): An article from: Validation Times
Speakers suggest strategies to meet new USP residual solven…
By: Rebecca Mashaw
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FDA questions process validity at Contract Medical Manufacturing.(Medical Devices): An article from: Validation Times
FDA questions process validity at Contract Medical Manufact…
By: Rebecca Mashaw
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Teva slammed with 16 GMP observations after audit of parenteral facility.(Human Drugs): An article from: Validation Times
Teva slammed with 16 GMP observations after audit of parent…
By: Rebecca Mashaw
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Medi-Stat cited for failure to conduct identity tests.(Human drugs): An article from: Validation Times
Medi-Stat cited for failure to conduct identity tests.(Huma…
By: Rebecca Mashaw
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Medical & Clinical Consortium slapped with 16-item 483.(Medical Devices): An article from: Validation Times
Medical & Clinical Consortium slapped with 16-item 483.…
By: Rebecca Mashaw
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Wyeth vaccine facility faulted for quality, production and laboratory system controls.(Biologics): An article from: Validation Times
Wyeth vaccine facility faulted for quality, production and …
By: Rebecca Mashaw
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Documentation failures at GE Healthcare IITS.(Medical Devices): An article from: Validation Times
Documentation failures at GE Healthcare IITS.(Medical Devic…
By: Rebecca Mashaw
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Cambrex warned about GMP violations at facility: Aug. 12-Milano, Italy.(Human Drugs): An article from: Validation Times
Cambrex warned about GMP violations at facility: Aug. 12-Mi…
By: Rebecca Mashaw
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Validation, documentation problems found at Contract Medical Manufacturing.(Medical Devices): An article from: Validation Times
Validation, documentation problems found at Contract Medica…
By: Rebecca Mashaw
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PMT failed to validate processes, FDA says in letter: Minneapolis District--Dec. 3.(Medical Devices): An article from: Validation Times
PMT failed to validate processes, FDA says in letter: Minne…
By: Rebecca Mashaw
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USP "open" to further delay in implementing Chapter <467>.(USP/PDA Conference): An article from: Validation Times
USP "open" to further delay in implementing Chapt…
By: Rebecca Mashaw
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Regulators, industry provide varying views on new residual solvents rules.(USP/PDA Conference): An article from: Validation Times
Regulators, industry provide varying views on new residual …
By: Rebecca Mashaw
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