Additionally Web-based Seminars

Oracle Database 10g: Administration Level I In this database administration course students gain the skills necessary for basic day-to-day administration of an Oracle10g database. This Oracle training class is the starting points for Oracle database administrators and also sets the foundation for advanced administrator training and certification. The class target audience is Oracle database administrators.  more...

Oracle Database 10g: Administration Level II ...s and perform actual recovery within the workshop. Additionally, some of the most exciting new technologies ever released by Oracle are considered within this training class. Subjects like the Database Scheduler, Flashback operations, Automatic Storage Management (ASM) and many others are included. This course book is filled with in-depth conceptual diagrams, hundreds of  more...

MOC 6451 - Planning, Deploying and Managing Microsoft System Center Configuration Manager 2007 This Configuration Manager training class provides students with the knowledge and skills to plan, deploy, and manage Configuration Manager 2007. The class focuses on planning and deploying sites and clients, configuring software distribution, deploying operating systems, and managing software updates. It also focuses on remote tools and managing mobile devices.This training class is intended for  more...

The Investigational Medicinal Product Dossier IMPD EU CTA vs FDA IND Comparing the Content and Agency Expectations - Webinar By Overview: This 90 minute training course will provide your company the opportunity for comprehensive understanding of the IMPD (Investigational Medicinal Product Dossier) and the structure and content differences between a EU CTA Application and an FDA IND Application. Additionally, this webinar covers many related processes sponsors will need to know, as they file for, conduct and close-out  more...

RAPS Approved Seminar on Risk Management in Pharmaceutical Industry at Mumbai ... how the implementation of strategies can mitigate risks. Additionally, the course provides trainees with skills to develop, deploy and extend the functionality of a risk management system by effectively analyzing and producing enterprise-wide risk management tools and measures. Specifically, it address the skills needed to acquire data from disparate data sources, develop appropriate risk  more...

The Investigational Medicinal Product Dossier IMPD EU CTA vs FDA IND Comparing the Content and Agency Expectation - Webinar By G This 90 minute training course will provide your company the opportunity for comprehensive understanding of the IMPD (Investigational Medicinal Product Dossier) and the structure and content differences between a EU CTA Application and an FDA IND Application. Additionally, this webinar covers many related processes sponsors will need to know, as they file for, conduct and close-out effective  more...

Elements of the Lot Disposition Process - Webinar By GlobalCompliancePanel ...s, and outline the expectations for documentation review. Additionally, the course will look at the creation of disposition packages for approval and rejection of materials, and cover changes in disposition status. The course will not cover the disposition of raw materials, third party (CMO) manufacturing, or validation lots. Why should you attend: The process for the disposition of  more...

Hazard Analysis vs FMECA Differences and Commonalities - Webinar By GlobalCompliancePanel ...ays how these tools can be used to complement each other. Additionally the differences and limitations of both methods will be illustrated and the appropriateness during the different product development phases will be discussed. Areas Covered in the Session: * Hazard analysis techniques * FMECA techniques * Probabilistic approaches * When to use which method during the  more...

Analytical Instrument and Equipment Qualification in Quality Laboratories - Webinar By GlobalCompliancePanel ...xicology studies and GCP labs supporting clinical trials. Additionally, labs supporting EPA studies are also regulated. This seminar will review the regulations that cover each environment and present simple and effective strategies for satisfying the requirements. The impact of USP on analytical instrument qualification will be reviewed and the newest regulation will be presented in a simple  more...

Complaint Handling in Compliance with FDA and ISO Regulations - Webinar by GlobalCompliancePanel This session will include the requirements for defining, documenting, and implementing a complaint-handling system, including the requirements for complaint review, investigation, and corrective action, as well as the ISO-specific implications. This session will discuss the best way to document customer feedback, what constitutes a complaint, and what do with "non-complaint" feedback. Also  more...

Full Day Virtual Seminar - Reduce Software Validation Costs and Pass the New 21 CFR Part 11 Inspections - Webinar by GlobalCompl This interactive one-day seminar details how to reduce costs associated with implementing, using, and maintaining computer systems in regulated environments. Nearly every computerized system used in laboratory, clinical, manufacturing and the quality process has to be validated. Participants will learn the latest techniques for complying with 21 CFR Part 11 that greatly reduce software  more...

Best Practices in Complaint Management - Compliance Webinar by GlobalCompliancePanel Negative customer feedback about a medical device's performance or safety is a strong indicator of whether a firm's manufacturing process is in control. This feedback is therefore subject to many requirements in both the QSR and ISO 13485. Failure to follow up on complaints about medical devices is among the most frequently cited observations on FDA-483s. This session will include the requirements  more...