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New Conferences and Training Courses:

Control of Drug-related Impurities, Degradants and Potential Genotoxic Impurities in Drug Substance and Drug Product

This course is designed to provide participants with an understanding of the regulatory expectations for controlling impurities, degradants and potential genotoxic impurities in drug…

Where: United States

FDA’s Proposed Rule Regarding Device Establishment Registration and Listing and How to Register and List

This Webinar will provide latest update as well as a “refresh” overview on how to register your device company and list your device(s) correctly…

Where: United States

The Disruptive Practitioner: Strategies for Corrective Action.

This webinar will discuss the development of such a policy, including a statement in the medical staff bylaws to the effect that each member…

Where: United States

Design Control and the ICH Q 10 Pharmaceutical Lifecycle

To define and explain the inputs and outputs of the design control process that that is inherent throughout the entire product lifecycle.

Event Venue: online

Attendance…

Where: United States

How to select Software for a Regulated Environment

There is fierce competition in the market, with multiple software vendors trying to convince to buy their product,these will be explained in this webinar….

Where: United States

Quality Systems Approach for the Pharmaceutical Lab: How to Prepare for a Successful Inspection

This course is designed to provide participants with an overview of some of the critical Quality Systems used in Pharmaceutical Laboratories to assure compliance…

Where: United States

Establishing adequate CAPA and Design Control procedures

This webinar is intended to provide guidance on understanding, interpreting, and implementing design control and CAPA system requirements.

Event Venue: online

Attendance cost (value and currency):…

Where: United States

Auditing Project Management Initiatives

It enables internal audit to be at the heart of what is happening and have the opportunity to influence decisions as they are made….

Where: United States

Batch Production Record and Device History Record Review and Quality Assessment

To determine compliance of the intermediates (FDA definition) and/or finished product with established specifications before a batch can be released for distribution BPRs, DHRs…

Where: United States

Pharmaceutical Manufacturing Batch Record Review

This program provides the foundation for an efficient and effective batch record review process and provides pharmaceutical companies with two strategies. First, the key…

Where: United States