News by Tag: Regulatory Compliance - Page 2
Design History Files (DHF), Device Master Records (DMR), Device History Records (DHR) -The Requi
February 26, 2013
Products made in the US have to meet global product design documentation specifications.
February 26, 2013
Products made in the US have to meet global product design documentation specifications.
RAPS pre-approved webinar on "Complaint Handling in Compliance with FDA and ISO Regulations" from GlobalCompliancePanel
February 26, 2013
GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, "Complaint Handling in Compliance with FDA and ISO Regulations" on March 5.
February 26, 2013
GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, "Complaint Handling in Compliance with FDA and ISO Regulations" on March 5.
Webinar on "Statistics for Quality Control and Process Validation: Statistical Process Control (SPC) for Attribute Data
February 26, 2013
GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, "Statistics for Quality Control and Process Validation: Statistical Process Control (SPC) for
February 26, 2013
GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, "Statistics for Quality Control and Process Validation: Statistical Process Control (SPC) for
RAPS pre-approved webinar on "Statistics for Quality Control and Process Validation: Statistical Process Control (SPC) for Variabl
February 26, 2013
Validation is not where atest method or manufacturing process ends. After this has been done, there is a need to continuously demonstrate that the procedure will operate consistently and reproducibly in a manner that meets the validation requirements
February 26, 2013
Validation is not where atest method or manufacturing process ends. After this has been done, there is a need to continuously demonstrate that the procedure will operate consistently and reproducibly in a manner that meets the validation requirements
GlobalCompliancePanel to organize RAPS pre-approved webinar on "Disinfection and Clean room Cleaning in an FDA Regulated Environme
February 26, 2013
GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, "Disinfection and Clean room Cleaning in an FDA Regulated Environment" on March 5, 2013.
February 26, 2013
GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, "Disinfection and Clean room Cleaning in an FDA Regulated Environment" on March 5, 2013.
RAPS pre-approved webinar on
February 26, 2013
"Medical Device Adverse Event Reporting Systems in EU, Canada and US" is the topic of a RAPS pre-approved webinar that GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize on March 6.
February 26, 2013
"Medical Device Adverse Event Reporting Systems in EU, Canada and US" is the topic of a RAPS pre-approved webinar that GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize on March 6.
ComplianceOnline Announces Seminar on Latin American Regulatory Requirements for Life Sciences Products
January 4, 2013
ComplianceOnline, the leading GRC advisory network, and well known regulatory affairs expert Robert J. Russell will conduct a two day seminar on Latin American regulatory compliance requirements for life sciences products.
January 4, 2013
ComplianceOnline, the leading GRC advisory network, and well known regulatory affairs expert Robert J. Russell will conduct a two day seminar on Latin American regulatory compliance requirements for life sciences products.
GlobalCompliancePanel to organize RAPS pre-approved webinar on "Excel Spreadsheets -Step-By-Step Instructions for Compliance"
November 23, 2012
David Nettleton, FDA Compliance Specialist, will be the speaker at aRAPS pre-approved webinaron the topic "Excel Spreadsheets -Step-By-Step Instructions for Compliance" that is being organized byGlobalCompliancePanel on December 5.
November 23, 2012
David Nettleton, FDA Compliance Specialist, will be the speaker at aRAPS pre-approved webinaron the topic "Excel Spreadsheets -Step-By-Step Instructions for Compliance" that is being organized byGlobalCompliancePanel on December 5.
"Dietary Supplement Regulatory Compliance in United States: Labeling, Product Claims & & Updates from the FDA"
September 21, 2012
GlobalCompliancePanel, a leading regulatory and compliance training provider, will organize a RAPS pre-approved webinar on the topic,"Dietary Supplement Regulatory Compliance in United States: Labeling, Product Claims & & Updates from the FDA" oct9
September 21, 2012
GlobalCompliancePanel, a leading regulatory and compliance training provider, will organize a RAPS pre-approved webinar on the topic,"Dietary Supplement Regulatory Compliance in United States: Labeling, Product Claims & & Updates from the FDA" oct9
2-day In-person Seminar on Regulatory Compliance for Dietary Supplements in the US, EU and Canada at Boston
August 20, 2012
James E Russell, a senior Regulatory Affairs professional, will host the seminar at Boston on September 13 and 14. Participants of this RAPS-approved seminar can earn 12 RAC points.
August 20, 2012
James E Russell, a senior Regulatory Affairs professional, will host the seminar at Boston on September 13 and 14. Participants of this RAPS-approved seminar can earn 12 RAC points.
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