Webinar-Import of FDA Regulated Products into US- - 0 views
-
Online Compliance on 04 Dec 14Webinar on the process of import of FDA-regulated products and common issues that importers of FDA-regulated products are likely to encounter.
Group items tagged
FDA Training-FDA 483 Letter-GCP Guidelines-CFR 21 - 0 views
-
Learn about Regulations, standards, guidance documents, records and reports associated to GCP, when and why FDA inspections are performed.
Procedures to Support Computer Systems Validation Regulated by FDA - 0 views
-
Learn policies and procedures required to support activities related to computer system validation for systems subject to FDA regulations in this webinar.
Equipment Validation-FDA Standards - 0 views
-
Get trained on practical aspects of FDA process validation, equipment qualification, Data analysis, statistical tools for Process Quality Management, more.
Computer System Validation to Mobile Applications-Live Training - 0 views
-
Learn how computer system validation can be applied to mobile applications subject to FDA regulations, what are the best practices, trends in validation.
Scale-Up and Post-Approval Changes - SUPAC Guidance - 0 views
-
Understand what kind of documentation is required while scaling-up or changing the equipment in your process, to comply with FDA SUPAC Guidance.
FDA Compliance-FDA Regulated Computer System Projects - 0 views
-
Learn about the best planning approach for guaranteeing foremost business edges and achieving Food and Drug Administration compliance through this webinar.
Corrective Actions - Current expectation of ISO 13485 and FDA auditors - 0 views
-
Webinar will provide an understanding of current expectations of ISO 13485 notified body auditors regarding containment or correction of nonconformity.
A Guide on Tobacco Prevention and FDA's deemed regulations - 0 views
-
This webinar will be addressing the updates in Tobacco Control Act Standards and FDA’s deemed regulations.
FDA Regulations for Importing-Exporting Medical Devices - 0 views
-
Attend this webinar to understand how to better manage your import and export compliance activities and help support your logistics supply chain.
eMDR Final August 14, 2015-eMDR Final Rule - 0 views
-
Learn about the FDA published final rule on Electronic Medical Device Reporting so that your company can be ready, and the requirements for submitting MDR reports electronically
Product Quality Reviews - FDA, EU and Canada Regulatory Requirements - 0 views
-
Attend this webinar to understand the world-wide regulatory requirements for Annual Product Reviews. Know the regulations governing product review.
510 (k) Applications- Medical Devices Software - 0 views
-
This webinar will discuss the structure and level of detail required in filing a 510k, when a medical device is software or contains software.
Drug Master Files-Requirements for GDUFA - 0 views
-
Webinar on GDUFA, know its background, Self-identification and fee requirements, how to achieve DMF “Available for Reference” status and more.
Complaint Handling in Compliance with FDA-ISO - 0 views
-
Learn about requirements for defining, documenting, implementing a complaint-handling system, complaint review, investigation, corrective action, more.
1 - 15 of 15
Showing 20▼ items per page