Merck KGaA-Pfizer to end late-stage ovarian cancer treatment study

FDA issues guidance on conducting remote interactive evaluations during the COVID-19 pandemic

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Form 424B5 Aptorum Group Ltd

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Bristol Myers scales up cell therapy production with liso-cel nod in hand and another approval …

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Iris Recognition in Access Control Market Trends, Analysis, Demand and Global Industry Research …

Download FREE sample copy of Iris Recognition in Access Control market report @ https://www.reportsanddata.com/sample-enquiry-form/483 …

EAS Due Diligence Assessments Support Private Equity and Venture Capital Firms with …

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Form 8-K Biohaven Pharmaceutical For: Mar 17

… manufactured or distributed by the Company (“Applicable Laws”); (ii) has not received any FDA Form 483, notice of adverse finding, warning letter, …

Trends In FDA Quality System Inspections: 3 Takeaways To Ensure Future Success

The Form 483 documents the regulatory clause(s) that is violated for the audited project and is informally provided to the team involved in the inspection …

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Merck KGaA and Pfizer Inc said on Friday they were ending a late-stage study for their drug to treat a form of ovarian cancer in previously untreated patients.