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Author: John Robinson
Displaying 261 to 270 of 270 articles < Back |
Pages: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27
 Articles by John Robinson 
261. GlobalCompliancePanelto organize RAPS pre-approved webinar on "Current Good Manufacturing Practice
October 14, 2012

Summary:“Current Good Manufacturing Practice for Medical Devices Including IVDs” is the topic of a RAPS pre-approved webinar that GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize on November 27.Dr. David Lim, a certified RAC and Certifi...

262. GlobalCompliancePanel to organize RAPS pre-approved webinar on "Lyophilization Process Development
October 14, 2012

Summary:“Lyophilization Process Development and Cycle Design with a Case Study” is the topic of aRAPS pre-approved webinar that GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize on November 15. Jeff Schwegman, Ph.D., founder and chief ex...

263. GlobalCompliancePanel to organize RAPS pre-approved webinar on "Obtaining an FDA Investigational De
October 14, 2012

Summary:GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will be organizing a RAPS pre-approved webinar on the topic, “Obtaining an FDA Investigational Device Exemption” on November 20. This webinar earns up to 1.0 RAC credits towards a participant's...

264. RAPS pre-approved webinar on "FDA Guidance Regarding Clinical Trials for Foods, Food Ingredients, a
October 14, 2012

AMAZINES.COM">Summary:A RAPS pre-approved webinar on the topic, “FDA Guidance Regarding Clinical Trials for Foods, Food Ingredients, and Dietary Supplements”, will be organized by GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, on November 20, 2...

265. RAPS pre-approved webinar on "21 CFR Part 11: Complying with Part 11 Regulation - Understanding the
October 14, 2012

Summary:GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, “21 CFR Part 11: Complying with Part 11 Regulation - Understanding the Predicate Rule”on November 6. Jasmin Nuhic, Senior Manager, Manufa...

266. RAPS pre-approved webinar on "FDA Inspections - Do's and Don'ts" from GlobalCompliancePanel
October 14, 2012

Summary:GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organizea RAPS pre-approved webinar o the topic,“FDA Inspections - Do's and Don'ts” onSeptember 25. Jeff Kasoff, RAC, Director of Regulatory Affairs at Life-Tech, Inc., will be the speaker...

267. RAPS pre-approved webinar on "Process Validation Principles and Protocols for Medical Devices" from
October 14, 2012

Summary:GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, “Process Validation Principles and Protocols for Medical Devices”, on November 15. Jeff Kasoff, RAC, Director of Regulatory Affairs at Li...

268. RAPS pre-approved webinar on "Design History File (DHF), Device Master Record (DMR), Device History
October 14, 2012

Summary:GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, “Design History File (DHF), Device Master Record (DMR), Device History Record (DHR) and Technical File (TF) –Regulatory Documents Explain...

269. RAPS pre-approved webinar on "Statistical Procedures Needed for Compliance with the Guidance on Pro
October 14, 2012

Summary:GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will conduct a RAPS pre-approved webinar on the topic, “Statistical Procedures Needed for Compliance with the Guidance on Process Validation”. The date of this webinar is November 14, and the s...

270. Overview: Course "The A to Z's of Microbial Control, Monitoring, Validation and Troubleshooting of
October 10, 2012

Overview: Course "The A to Z's of Microbial Control, Monitoring, Validation and Troubleshooting of Pharmaceutical Water Systems" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. In order to understand the microbiology ...

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I am the editor of QUAY Magazine, a B2B publication based in the South West of the UK. I am also the...more

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