Facility Web-based Seminars

Live Online Course for gaining PDUs Towards the advancement of Project Management knowledge, after acquiring PMP Certification you require continuing the certificate (CCR).Certificate is valid for 3 years & 60 professional development units (PDUs) are required during each three-year certification/ CCR cycle. PMSoft provides facility to earn PDUs through Free Live, Online PDU Sessions on various topics related to Project,  more...

Introduction to Spring Training ...cus on the " Core " module of the framework, developing facility in instantiating, configuring, and assembling Spring beans for various purposes. The Core module gives the developer declarative control over object creation and assembly; this is useful for any tier of any Java application. So is Spring ' s validation framework, and so we study not only the assembly of object graphs, but  more...

Preserving Precious Capital Attacking the SEVEN Most Significant Capital Wasters in Your Company Times are tough and capital preservation is at the top of every executivea ™s priority list. But specific techniques necessary to rapidly eliminate waste and reduce operating costs can be difficult to define and even more difficult to implement. If you manage ANY type of an organization, you have waste which steals precious capital from your enterprise. Now, more than ever, it is important  more...

What to do if you get a FDA 483 Warning Letter - Webinar By GlobalCompliancePanel Overview: Audits by the FDA are perhaps the most intimidating of all events at a regulated facility. Each year, the FDA conducts several thousand audits, approximately half of which lead to findings that result in Form 483s. Thursday, March 29, 2012 10: 00 AM PDT | 01: 00 PM EDT  more...

How to Survive a DEA Inspection Series For a Research Facility - Webinar By mentorhealth The training will cover DEA record-keeping and effective security that DEA registrant must comply with when handling controlled substances. It covers elements of what occurs during an unannounced inspection and the auditing methods. Thursday, December 1, 2011 10: 00 AM PST | 01: 00 PM EST  more...

Pharmaceutical and Biologics Facility Design FDA and Regulatory Aspects by gcp This course explores some of the best practices of pharmaceutical facility design with an emphasis on the regulatory aspect.  more...

Risk-Based Validation for GxP Facilities - Webinar By GlobalCompliancePanel This presentation teaches a practical methodology for creating and applying Risk-Based Equipment Validation. It shows an example of how this process may be integrated into a facility Master Validation Plan  more...

Developing the Master VV Plan to Meet US FDA ISO 13485 and 14971 Requirements - Webinar By GlobalCompliancePanel ...from process / equipment V&V * Process / Equipment / Facility Validation - FDA's new guidance * When and How to use DQ, IQ, OQ, PQ, or their equivalents * How to use Product Risk Management Tools (per ISO 14971 and ICH Q9) * The 11 key documents for software validation * Incorporating 21 CFR Part 11 requirements * Suggested "test case" formats Who will benefit:  more...

Reprocessing REUSABLE Medical Devices-Cleaning Labeling Requirements - Webinar By GlobalCompliancePanel ...edical device. If intended to be resterilized by the user facility, cleaning & sterilization instructions must be precise and validated. Areas Covered in the Session: * Reasoning behind labeling requirements * Regulatory requirements * Intended use & design * Standards/ guidance * Validating cleaning & sterilization Who Will Benefit: * Design Engineers  more...

Analytical Instrument and Equipment Qualification in Quality Laboratories - Webinar By GlobalCompliancePanel Overview: The analytical instruments and equipment used in GXP laboratories must be calibrated and qualified for use in regulated testing. This includes quality control labs attached to cGMP facilities, GLP labs supporting animal toxicology studies and GCP labs supporting clinical trials. Additionally, labs supporting EPA studies are also regulated. This seminar will review the regulations that  more...

Medical Device Tracking Latest FDA Update and Expectations - Webinar By GlobalCompliancePanel ...ning or life-supporting device used outside a device user facility. Section 519(e), as revised by FDAMA, states the agency may require tracking for a class II or class III devices: (A) the failure of which would be reasonably likely to have serious adverse health consequences; or (B) which is intended to be implanted in the human body for more than one year; or (C) which is a life sustaining or  more...

Crisis Management and Risk Communication - Webinar by GlobalCompliancePanel As your company's system continues to grow, the potential for "crisis issues" to occur grows proportionally. The concern for food safety to your customers and employees must be a constant area of focus for all operators in the system. Ultimately, how well your company manages the crisis situations it will make a significant difference in how your company brand is perceived in the public's eyes  more...

Siebel CRM Training - Online SiebelTraining. org provides the facility of online trainings via web/ video conference, especially for its trainees in US, UK, Australia, Canada, Europe, Middle East, Singapore, Malaysia and China. All the courses offered by us in classroom sessions are also offered via the online platform but with more emphasis on quality given the one-to-one interactions.  more...