7 Quality Control Tools Web-based Seminars
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From Manufacturing Executive Institute
A Case for Routine Use of Statistical Process Control SPC in Manufacturing
You are invited to attend the Manufacturing Executive Institutea ™s FREE June 2012 3rd Thursday - a Operations Improvement webinar, A Case for Routine Use of Statistical Process Control (SPC) in Manufacturing.
Statistical Process Control is a term that describes a process for predicting failures and methodically determining the underlying cause(s) before the predicted failures can
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Better Methods To Control Tools Fixtures in Production
Manufacturing ANYTHING requires tools, fixtures and supplies; in addition to people, machines, materials and methods. And while most improvement initiatives focus on production methods and material availability, it is often the tools and fixtures that cause manufacturing disruptions, sometimes leading to shipping delays and customer dissatisfaction. How many times have you been ready to produce,
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From GlobalCompliancePanel
Preventing Food Safety Problems BY GCP
Most industries have become reasonably sophisticated in terms of applying the principals and tools involved in quality control and improvement.
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Facilities Cleaning in Cleanrooms and Controlled Environments - Webinar By GlobalCompliancePanel
Overview: This live webinar concentrates on proper cleanroom cleaning, and discusses tools, equipment, agents, personnel training, extent, and frequencies.
It is a very practical training session intended to assist personnel involved in the design, cleaning, monitoring, and assessment of cleanroom cleaning procedures. The key benefits of this course are:
* In-dept understanding of
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Project Management for Clinical Trials - Webinar By GlobalCompliancePanel
Overview: This web seminar has been designed to provide you with a clear understanding of project management skills to apply to running clinical trials.
It will ensure you gain a clear understanding of the tools and techniques of project management for clinical trial and how they can be applied to your own pharmaceutical projects in the work place. In addition to key project management tools
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Change Control -- Your Companys GMP Weak Point - Webinar By GlobalCompliancePanel
Overview: There is a pervasive public perception that the FDA has been ineffective in protecting the public.
Recent news events in foods, drugs, and devices seem to support this perception. The "tougher" FDA is determined to change that perception. Industry must be prepared to adapt, and recognize that such adaptation will actually work to their long-term benefit. This webinar will discuss and
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Process Validation current industry practices and FDA Guidance Document Review - Webinar by GlobalCompliancePanel
Overview: Process Validation is required by FDA and most regulatory bodies. PV demonstrates consistency of pharmaceutical processes.
PV requires writing and executing a validation protocol that explores either natural variation or introduced variation in a process and shows that the process can consistently produce a quality product. Writing and executing good process validation can be a
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Medical Device Changes and The 510k - Webinar By GlobalCompliancePanel
Overview: This webinar will examine the broad range of issues to be considered by a company when reviewing
1) A series of minor changes or
2) One major change to an existing product having an existing 510(k), for the need for a new 510(k).
Such a review takes on added urgency as a result of the stated intent of the Agency to get tougher across the board in its expectations for the medical
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Project Management in a cGMP Environment - Webinar By GlobalCompliancePanel
Overview: This webinar will provide valuable guidance to regulated companies in development and implementation of Project Management Planning and Techniques for new product development, regulatory compliance audit responses, proof of "progress against plan", and other activities requiring a planned documented rationale.
Three of the most common tools will be discussed. One very simple approach
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Legal Risks in Social Media for Healthcare Providers - Webinar By GlobalCompliancePanel
Overview: Most sophisticated businesses use social media sites such as Facebook, MySpace, Twitter, and LinkedIn to promote their services, connect with their customers, and as a overall component of their business strategy.
Physicians and other healthcare providers have begun to experiment in the social media environment, but most are concerned that the special rules applicable to the
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Chemical Control for Food Manufacturers Ingredient Cleaning and Hazardous Materials - Webinar By GlobalCompliancePanel
Overview: A comprehensive review of an ideal chemical control program will be presented.
The guidelines presented will enable your company to implement programs that are cost effective and meet or exceed the expectations of major QSR, and GFSI audit criteria. This presentation will provide not only a provide schematic for management and control of chemicals, but an interactive and customizable
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Avoiding FDA 483 Observations by Identifying the Root Cause of Deviations - Webinar By GlobalCompliancePanel
Overview: Recent Consent Decrees have included requirements that the firm develop and implement systems that result in timely and complete investigations of deviations and corrective and preventive actions that address the root cause of deviations.
FDA 483 and Warning letter observations identify inadequate investigations and follow-up. This webinar addresses adequate investigation of
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Preventive and Corrective Maintenance Protect your assets Protect your consumers - Webinar By GlobalCompliancePanel
Overview: A how to guide to meeting customer expectations of the maintenance function.
An overview of industry best practices and a review of some leading software solutions.
Why you should attend: Maintenance is often found to present the greatest area of opportunity for improvement in the food safety chain. Lack of control of parts and condition of equipment often contributes foreign
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How to Prevent Food Safety Problems Using Your Current Quality System - Webinar by GlobalCompliancePanel
Most industries have become reasonably sophisticated in terms of applying the principals and tools involved in quality control and improvement.
Unfortunately, food supply chain members have lived outside of the quality world and have not invested the time, training or money to learn and apply the disciplines needed to bring quality into preventive levels of control. Visual inspection in many
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Robust Process Validation for Medical Devices - Webinar by GlobalCompliancePanel
One of the most common reasons noted by the FDA for recalls of medical device is improper validation.
It is also one of the most common reasons companies receive 483s and warning letters. Conversely, successful validations not only satisfy compliance and regulatory requirements, they also provide for robust manufacturing processes satisfying the needs of many individual functions within your
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Outsourced processes and ISO 90012008 - Webinar by GlobalCompliancePanel
In 2008, a new edition of ISO 9001 went into effect. The literature says the new version doesn't introduce any new requirements but only clarifications to the existing requirements.
One of the clarifications involves the use of Outsourced Processes in the Quality Management System. The changes clarify the organization's responsibility for conformity to all customer, regulatory, and statutory
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From iGallant Solutions
Six Sigma Green Belt SSGB
Six Sigma Green Belt
Online Live Instructor / Classroom Training
Six sigma Overview
Six Sigma seeks to identify and remove the causes of defects and errors in manufacturing and business processes. It uses a set of quality management methods, including statistical methods, and creates a special infrastructure of people within the organization ("Green Belts, Black Belts" etc.) who are
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From Global BioPharmaceutical Resources, Inc. (GBPR, Inc.)
How to be Compliant and competitive
For healthcare companies compliance with all applicable regulations is imperative and it is usually well understood how this can be achieved. However, in a highly competitive and increasingly global marketplace, mere compliance is insufficient for success. Competitiveness must be achieved not only through cost efficient manufacture and supply, but also by achieving compliance at the right cost
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