Pharma Training News

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Latest News: Article

  • Daily Dose Digest Week October 31st - November 4th, 2016

    • 4 weeks ago

    FDA Regulatory and Compliance News FDA’s Center for Devices and Radiological Health (CDRH) announced the...

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  • Daily Dose Digest Week October 17th-24th, 2016

    • 1 month ago

    FDA Regulatory and Compliance News FDA’s Bone, Reproductive and Urologic Drugs Advisory Committee (BRUDAC) supported,...

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  • NSF International’s Peter Gough Receives Honorary Doctorate Degree From Kingston University

    • 4 months ago

    On July 27, 2016, Peter Gough, Executive Director of NSF Health Sciences Pharma Biotech, was...

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  • UK Health Sciences Brexit Implication Statement

    • 5 months ago

    Brexit Implications for UK Pharmaceutical Administration By Peter Gough and the NSF Health Sciences team...

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  • NSF International Announces Center of Excellence for Pharmaceutical Development

    • 7 months ago

    ANN ARBOR, Mich. and BRISTOL, Conn. – NSF International, a global public health organization, has...

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  • NSF First to Earn ANSI Accreditation to Certify Manufacturers to Current GMP Standard

    • 1 year ago

    ANN ARBOR, Mich. and ARLINGTON, Va. – NSF Health Sciences Certification, LLC (NSF), which provides...

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  • NSF International Strengthens Medical Device Consulting With Acquisition of Avarent LLC

    • 1 year ago

    ANN ARBOR, Mich. and LIBERTYVILLE, Ill. – NSF International, a leading provider of regulatory compliance,...

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  • National Standard for Excipient Good Manufacturing Practices Published by NSF International

    • 2 years ago

    ANN ARBOR, Mich. – Global public health organization NSF International has published the first American...

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  • How to Effectively Respond to FDA 483s

    • 2 years ago

    By Kristen Grumet. Posted in Regulatory and Compliance by MDDI Staff

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  • Qualified Persons Declaration Template and Guidance Published by EMA

    • 2 years ago

    The long-awaited Qualified Persons template for declarations concerning Good Manufacturing Practice compliance of active substances...

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  • New Name for the Irish Medicines Board Goes Into Effect July 1, 2014

    • 3 years ago

    On July 1, 2014, the Irish Medicines Board (IMB) will change its name to the...

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  • New EU Clinical Trial Regulation Approved by the European Parliament

    • 3 years ago

    On 2 April 2014 the text of the new CT Regulation, which will replace the...

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  • Critical Decisions in Medical Devices

    • 3 years ago

    The medical device industry faces dramatic changes in the way it is regulated, particularly in...

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  • European Medicines Agency Launches Adaptive Licensing Pilot Project

    • 3 years ago

    To improve timely patient access to new medicines, the European Medicines Agency (EMA) launched a...

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  • CDSCO (India) Announced That Imported Drug Products Must Meet Indian Medicinal Products Requirements

    • 3 years ago

    The Indian drug regulatory agency Central Drugs Standard Control Organization (CDSCO) announced on March 4...

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