Enhanced Validation Plans to Meet FDA Expectations and Mitigate Risk Seminar: Addressing GMP Deficiencies through Risk-Based Validation Strategies
02 sept. 2024 06h28 HE
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Research and Markets
Dublin, Sept. 02, 2024 (GLOBE NEWSWIRE) -- The "Master Validation Plan - The Unwritten Requirements" report has been added to ResearchAndMarkets.com's offering. Master Validation Planning...
Risk Management of Raw Materials in a GMP Environment Course (ON-DEMAND)
02 sept. 2024 05h10 HE
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Research and Markets
Dublin, Sept. 02, 2024 (GLOBE NEWSWIRE) -- The "Risk Management of Raw Materials in a GMP Environment Course" training has been added to ResearchAndMarkets.com's offering. Risk management of raw...
Thinking Outside of the GMP (Good Manufacturing Practice) Box Training Course with Speaker, Mustafa Edik - An Independent GMP Consultant and Auditor (ON-DEMAND)
18 juil. 2024 04h09 HE
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Research and Markets
Dublin, July 18, 2024 (GLOBE NEWSWIRE) -- The "Thinking Outside of the GMP (Good Manufacturing Practice) Box Training Course" conference has been added to ResearchAndMarkets.com's offering. When...
Panthera BioSolutions Launches Pharmaceutical Good Manufacturing Practice (GMP) Foundational Training Course with Dallas College to Advance Workforce Talent Pipeline in North Texas
15 juil. 2024 11h57 HE
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BHIANT
DALLAS, July 15, 2024 (GLOBE NEWSWIRE) -- The Biotechnology and Healthcare Industry Alliance of North Texas (BHIANT) is proud to announce a strategic partnership between Dallas College and Panthera...
Quality Control Laboratory Compliance - cGMPs and GLPs Course (2-Day Online Event, November 7-8, 2024)
03 juil. 2024 11h21 HE
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Research and Markets
Dublin, July 03, 2024 (GLOBE NEWSWIRE) -- The "Quality Control Laboratory Compliance - cGMPs and GLPs Course" training has been added to ResearchAndMarkets.com's offering. The pharmaceutical...
US FDA QMSR ( Quality Management System Regulation) Transition Course: Harmonization of 21 CFR 820, Device CGMPs (QSR), to the ISO 13485 (ON-DEMAND)
28 juin 2024 10h48 HE
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Research and Markets
Dublin, June 28, 2024 (GLOBE NEWSWIRE) -- The "The US FDA QMSR Transition - 21 CFR 820 and ISO 13485" training has been added to ResearchAndMarkets.com's offering.The US FDA, after years of...
Annual GMP Master Class 2024 to Elevate Pharmaceutical Manufacturing Standards
27 juin 2024 10h15 HE
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Research and Markets
Dublin, June 27, 2024 (GLOBE NEWSWIRE) -- The "Annual GMP Master Class 2024" report has been added to ResearchAndMarkets.com's offering.The Annual GMP Master Class of 2024 is poised to...
FDA QMSR and the Key Elements of QSIT cGMP Inspection and Audits for Medical Device Manufacturers (ON-DEMAND COURSE)
27 juin 2024 10h01 HE
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Research and Markets
Dublin, June 27, 2024 (GLOBE NEWSWIRE) -- The "The FDA QMSR and the Key Elements of QSIT cGMP Inspection and Audits for Medical Device Manufacturers" training has been added to ...
GMP Auditing for Quality Assurance Training Course for FDA Regulated Industries (2-Day Virtual Course: September 4-5, 2024)
28 mai 2024 04h11 HE
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Research and Markets
Dublin, May 28, 2024 (GLOBE NEWSWIRE) -- The "GMP Auditing for Quality Assurance Training Course for FDA Regulated Industries" training has been added to ResearchAndMarkets.com's offering. ...
Successful FDA Inspection at Dipharma Facility in Kalamazoo, MI, USA
07 mai 2024 10h00 HE
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Dipharma Francis S.r.l
Dipharma Inc. has been inspected by the US FDA and has received the EIR, satisfactorily closing the inspection process.