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Find FDA inspection courses, FDA training, FDA conferences, FDA seminars, FDA workshops, FDA webinars, FDA on-line training on FDA inspecitons, GLP inspections, Pre-Approval inspections, GMP inspections, HAACP inspections, QSIT inspections, QSR inspections, Food inspections, Pharmaceutical inspections, Biologics inspections, clinical trial inspections, nutraceutical inspecitons, dietary supplement inspections. Resources to prepare for, faciliate or remediate your FDA pharmaceutical, medical device, biologic, food, cosmetic, dietary supplement, clinical trials inspections.

2011 FDA Inspection Calendar
USA FDA inspection related courses, conferences, on-line training, webinars, seminars

Are you an US Food and Drug Administration regulated pharmaceutical, medical device, biological, food, cosmetic or dietary supplement manufacturer preparing for an USFDA inspection ? Want to attend training courses on FDA inspections, Good Manufacturing Practices, or Good Laboratory Practices ? Submit US FDA inspection Training Requests.
2011 US FDA inspection Training Courses, Workshops, Conferences, Seminars, Webinars, On-Line Training Courses
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US FDA training course, workshop, webinar, seminar, conference, online training description.
01/18/2011
How to Prevent or Handle Protocol Deviations and Violations to be GCP and Regulatory Compliant? - Webinar By GlobalCompliancePanel
 How to Prevent or Handle Protocol Deviations and Violations to be GCP and Regulatory Compliant? - Webinar By GlobalCompliancePanel
Sponsor: Global Compliance Panel
03/10/2011
How to Write SOPs: Tips on Writing the Perfect Document to Impress the FDA
 How to Write SOPs: Tips on Writing the Perfect Document to Impress the FDA
Sponsor: Compliance Online
03/10/2011
Webinar On Differences between ICH-GCP and FDA regulations
 Webinar On Differences between ICH-GCP and FDA regulations
Sponsor: Compliance Online
03/15/2011
Bringing Compliance To Design Control For Older Products - Webinar By GlobalCompliancePanel
 Bringing Compliance To Design Control For Older Products - Webinar By GlobalCompliancePanel
Sponsor: Global Compliance panel
03/17/2011
 Medical Device Complaints, MDR's and Recalls
Sponsor: Compliance Online
03/22/2011
An Introduction to FDA's Regulation of Human Cells, Tissues, and Cellular and Tissue-Based Products
 An Introduction to FDA's Regulation of Human Cells, Tissues, and Cellular and Tissue-Based Products
Sponsor: Compliance Online
03/29/2011
Preparing for FDA GCP Inspections - Essentials for Sponsors and Clinical Sites
 Preparing for FDA GCP Inspections - Essentials for Sponsors and Clinical Sites
Sponsor: Compliance online
04/07/2011
 Basics of testing associated with sterilization validation and routine processing
Sponsor: Compliance Online
04/07/2011
Understanding ISO 13485 vs. ISO 9001 for Successful QMS in Medical Device Industries - Webinar By GlobalCompliancePanel
 Understanding ISO 13485 vs. ISO 9001 for Successful QMS in Medical Device Industries - Webinar By GlobalCompliancePanel
Sponsor: Global Compliance Panel
04/07/2011
 Understanding ISO 13485 vs. ISO 9001 for Successful QMS in Medical Device Industries - Webinar By GlobalCompliancePanel
Sponsor: Global Compliance Panel
04/13/2011
Off-Label Promotion of Medical Devices: Maximizing Your Performance Claims within FDA's Framework of Acceptable Practices - Webinar By GCPanel
 Off-Label Promotion of Medical Devices: Maximizing Your Performance Claims within FDA's Framework of Acceptable Practices - Webinar By GCPanel
Sponsor: Global Compliance Panel
04/13/2011
Off-Label Promotion of Medical Devices: Maximizing Your Performance Claims within FDA's Framework of Acceptable Practices - Webinar By GCPanel
 Off-Label Promotion of Medical Devices: Maximizing Your Performance Claims within FDA's Framework of Acceptable Practices - Webinar By GCPanel
Sponsor: Global Compliance Panel
04/19/2011
 Design History Files, Device Master Records, Device History Records, and Technical Files
Sponsor: Compliance Online
05/03/2011
 FMEA and Risk Management for Medical Devices - Webinar By GlobalCompliancePanel
Sponsor: global Compliance Panel
05/03/2011
 FMEA and Risk Management for Medical Devices - Webinar By GlobalCompliancePanel
Sponsor: Global Compliance Panel
05/05/2011
 Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs) - Webinar By GlobalCompliancePanel
Sponsor: Global Compliance Panel
05/05/2011
Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs) - Webinar By GlobalCompliancePanel
 Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs) - Webinar By GlobalCompliancePanel
Sponsor: Global Compliance Panel
05/10/2011
Using Statistics to Determine Sample Size - Webinar By GlobalCompliancePanel
 Using Statistics to Determine Sample Size - Webinar By GlobalCompliancePanel
Sponsor: Global Compliance Panela
05/10/2011
Using Statistics to Determine Sample Size - Webinar By GlobalCompliancePanel
 Using Statistics to Determine Sample Size - Webinar By GlobalCompliancePanel
Sponsor: Global Compliance Panel
05/17/2011
 Designing a CAPA System that Meets and Exceeds Regulatory Requirements - Webinar By GlobalCompliancePanel
Sponsor: global Compliance Panel
05/17/2011
 Designing a CAPA System that Meets and Exceeds Regulatory Requirements - Webinar By GlobalCompliancePanel
Sponsor: Global Compliance Panel
05/19/2011
 Recalls & Vigilance - When to Report Complaints - Webinar By GlobalCompliancePanel
Sponsor: Global Compliance Panel
05/19/2011
 Recalls & Vigilance - When to Report Complaints - Webinar By GlobalCompliancePanel
Sponsor: Global Compliance Panel
06/15/2011
 The 510(k) Submission: Requirements, Contents, and Options - Webinar By GlobalCompliancePanel
Sponsor: Global Compliance Panel
06/16/2011
 Understanding and Implementing USP 1058: Analytical Instrument Qualification - Webinar By GlobalCompliancePanel
Sponsor: Global Compliance Panel
06/22/2011
 What to Expect and How to Prepare for FDA Inspections - By GlobalCompliancePanel
Sponsor: Global Compliance Panel
07/18/2011
 WORLDx Congress
Sponsor: Institute for International Research
07/18/2011
 WORLDx Congress
Sponsor: Institute for International Research
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2011-10-26 00:00:00
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2011-10-19 00:00:00
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2011-10-19 00:00:00
The U.S. Food and Drug Administration has issued a proposed rule and dr... FDA approves Ferriprox to treat patients with excess iron in the body
2011-10-19 00:00:00
The U.S. Food and Drug Administration today approved Ferriprox (deferiprone... FDA: U.S. Marshals seize foods stored at Washington State facility FDA inspection found rodent and insect infestation
2011-10-11 00:00:00
At the request of the U.S. Food and Drug Administration, U.S. Marshals seiz... FDA, CMS launch pilot program for voluntary parallel review of innovative devices Aim is to reduce time between FDA approval and CMS national coverage determinations
2011-10-07 00:00:00
The U.S. Food and Drug Administration and the Centers for Medicare & Medica... FDA approves Cialis to treat benign prostatic hyperplasia
2011-10-06 00:00:00
The U.S. Food and Drug Administration today approved Cialis (tadalafil) to ... FDA and NIH announce joint study on tobacco use and risk perceptions Landmark collaboration is the first since the passing of the 2009 Tobacco Control Act
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The U.S. Food and Drug Administration and the National Institutes of Health... FDA commissioner outlines steps to spur biomedical innovation, improve health of Americans
2011-10-05 00:00:00
FDA Commissioner Margaret A. Hamburg, M.D., today released a blueprint cont... FDA outlines plans for an outside network of scientific experts Network will help quickly address regulatory concerns, broaden staff knowledge of new and emerging technologies
2011-10-04 00:00:00
FDA's Center for Devices and Radiological Health (CDRH) is soliciting comme... FDA awards three grants to stimulate development of pediatric medical devices Grantees will work with industry and the FDA to address unmet pediatric device needs
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The U.S. Food and Drug Administration today announced the awards of three g...
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