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Thursday, August 22, 2013
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Process Validation for Medical Devices
August 21, 2013 at 8am to August 22, 2013 at 5pm – Courtyard Marriott Boston ,MA 02139, USA Medical device manufacturers can avoid FDA Warning Letters, 483s and enforcement actions with a good understanding process validation principles. But knowing how to proceed is the toughest task as no… Organized by ComplianceOnline | Type: seminar
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Latin America: Regulatory Compliance Requirements for Life Science Products
August 22, 2013 at 8am to August 23, 2013 at 4:30pm – Courtyard Philadelphia Downtown his two-day comprehensive Course on Latin America Regulatory compliance requirements will cover topics ranging from pre-clinical and clinical requirements through product registration, amendments and… Organized by ComplianceOnline | Type: seminar
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