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Searching Content indexed under Product Liability & Safety by Chiang Ling Li ordered by Published Date Descending.
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UK Regulator Recalls Progesterone Produced By India-Based Akums Drugs And Pharmaceuticals
The Statement of Non-Compliance with GMP published on the EudraGMP website noted that one critical and three major deficiencies were uncovered during the inspection.
UK
21 Jul 2016
2
FDA Proposes Rule On Classification Of Pediatric Medical Crib And Pediatric Medical Bassinet
In the October 8, 2015, Federal Register, FDA proposed to rename pediatric hospital beds as pediatric medical cribs and establish special controls for these devices.
United States
6 Nov 2015
3
FDA Issues Notice Of Enforcement Action Against Unapproved Prescription Ear Drop Products
On July 1, 2015, FDA announced it will begin taking enforcement action against companies that manufacture or distribute certain unapproved prescription ear drop products, known as otic products.
United States
3 Aug 2015
4
European Court Hands Down Judgment In Medical Device Case
The Bundesgerichtshof asked the Court of Justice whether the device may be classified as defective based solely on evidence that quality control checks on devices of the same model disclosed a potential defect.
European Union
17 Mar 2015
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