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Qualification Training Seminars and Classes

From Internet English Learn Online

Exam Preparation ... exam you are studying for, an internationally recognised qualification in English or an end-of-year school exam, IELO can help you achieve your goals! Students who wish to study these, or any other English exams, must be focused and prepared for intense English grammar and vocabulary based lessons. IELO's curriculums focus on use of English vocabulary, grammar and pronunciation in all of more...

From GlobalCompliancePanel

Change Control Management From Design to Commercialization - Webinar By GlobalCompliancePanel There is a need to implement an adequate formal level of change control during engineering projects (referred to as an Engineering Change Control) after the approval of the equipment/ systems specifications in addition to the more formal change control after the qualification of these systems. Thursday, January 12, 2012 10: 00 AM PST | 01: 00 PM EST more...

New Process Validation Life-Cycle Approach - Apply statistical tools to demonstrate Process Capability - Webinar By GlobalCompli This webinar will describe the new Process Validation Life-Cycle Approach as defined in the revised FDA guideline. The three stages will be described in detail including: Process Design, Process Qualification and the Continued Process Verification. Thursday, December 15, 2011 10: 00 AM PST | 01: 00 PM EST more...

Does your Equipment Program Meet Current Regulatory Expectation - Webinar By GlobalCompliancePanel This Interactive webinar will begin with an overview of the GMP/ GLP requirements for an Equipment system. The procedure for Equipment Qualification will be discussed. The system elements required to manage the maintenance and calibration of all equipment in the laboratory will be discussed. The documentation which is critical for GMP/ GLP compliance will be reviewed. Thursday, October 20, 2011 more...

Establishing a Reduced Testing Program for Pharmaceutical Medical Device Components ... are adequate controls on specification control, material qualification, supplier qualification & monitoring, material validation, and collaborative testing. Industry practice in the performance of reduced testing has resulted in new and modified expectations and requirements. The benefits of systematic reduced testing program include increased compliance, smaller inventory cycles, less more...

Understanding and Implementing USP 1058 Analytical Instrument Qualification - Webinar By GlobalCompliancePanel ...ty for the intended use. Despite the fact that instrument qualification is nothing new and companies spend a lot of time, it is a frequently cited deviation in FDA inspectional observations and warning letters. Companies are unsure on what exactly to qualify or re-qualify, test and document. The main reason is that unlike for analytical methods there are no clear standards for equipment more...

Vendor Qualification Auditing for FDA Computer System Compliance - Webinar By GlobalCompliancePanel This Vendor Qualification training will include sample forms and checklists which may be used by the participants, along with some initial training on the appropriate use of forms and checklists more...

Pharmaceutical and Medical Device Validation Guidances - Similarities and Differences - Webinar By GlobalCompliancePanel ... Protocol Approval Process for Installation & Operational Qualification and Process Validation * Executing the Protocols * Reviewing the Issue Protocols, Taking Appropriate Actions, and Writing the Report * Revalidation Who Will Benefit: * Quality, quality control, regulatory, engineering, and manufacturing and IT staff working in the FDA regulated industry in the more...

Gowning Systems Used in Cleanrooms Controlled Environments - Webinar By GlobalCompliancePanel Overview: This live webinar concentrates on identifying cleanroom garment systems, how they should be used, management of their supply, and control of human variables. Key benefits of this seminar include: * In-dept understanding of cleanroom garments and their use. * Reduce personnel-related environmental contamination issues. * Achieve satisfactory inspections more easily. more...

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 more...

Calibration and Qualification in Analytical Laboratories - Webinar By GlobalCompliancePanel ... quality. Despite the fact that equipment calibration and qualification is nothing new and companies spend a lot of time, it is a frequently cited deviation in FDA inspectional observations and warning letters. Companies are unsure on what exactly to qualify test and document. For easy implementation, attendees will receive: * 4 SOPs o User Requirement Specifications (URS) more...

Validating Rapid Microbiological Methods - Webinar By GlobalCompliancePanel ... * User requirements specifications (URS) * Design Qualification (DQ) * Supplier assessment/ audit * Functional design Specifications (FDS) * Requirements Traceability Matrix (RTM) * Developing test plan, including installation, operational and performance qualifications (IQ, oq and PQ) * Pharmacopoeia testing requirements from the United States and European more...

Purchasing and Supplier Controls in the Medical Device Industry - Webinar By GlobalCompliancePanel ...qualification and assessment is required in both the QSR regulations and ISO standards. Many companies spend a great deal of time and money in pursuit of compliance with this. Many companies can spend MUCH LESS time and money, and still be in control of their suppliers and in compliance with the regulations. This presentation will review the QSR and ISO requirements for supplier evaluation more...

Does your Equipment Program meet current regulatory expectations - Webinar By GlobalCompliancePanel ...s for an Equipment system. The procedure for Equipment Qualification will be discussed. The system elements required to manage the maintenance and calibration of all equipment in the laboratory will be discussed. The documentation which is critical for GMP/ GLP compliance will be reviewed. Why you should attend: The equipment Program is a critical component of both GMP and GLP more...

Operational Risk Management Ensuring Safety for Food Systems - Webinar By GlobalCompliancePanel ...erica is falling further behind. * A sample supplier qualification system based on food safety risk predictors. * A model for retail driven risk reduction based on supplier typologies Who will benefit: * Food supply chain buyers (farms, wholesalers and distributors, retailers, packers, restaurants, and processors) and corporate executives need to be updated and on top of how more...

Analytical Instrument and Equipment Qualification in Quality Laboratories - Webinar By GlobalCompliancePanel ...requirements. The impact of USP on analytical instrument qualification will be reviewed and the newest regulation will be presented in a simple and understandable way. The interaction of calibration, qualification, method validation and equipment maintenance on laboratory compliance and data quality will be discussed. Why should you attend: The analytical instruments and laboratory more...

Designing and Implementing the Quality System for Combination Products - Webinar By GlobalCompliancePanel ... Module 6: Material a Purchasing Controls-Specification, Qualification and Control of Suppliers, and controlling incoming materials Module 7: Technical and "Administrative" Process Controls Module 8: Introduction to Deviations & Quality Failures (0: 10) Module 9: Validation Module 10: Maintaining Label Control-From Design to Label Application Module 11: Storage and Distribution & Returned more...

Transfer of Analytical Methods FDA Expectations and Tools for Implementation - Webinar by GlobalCompliancePanel ...onsistent and reliable analytical test methods. Method qualification of a method can be achieved in three ways: Validation, Verification (Compendial Methods) and Method Transfer (company methods). Lack of such documentation can result in warning letters from both the FDA and Health Canada. This webinar discusses how to execute meaningful Method Transfers of company methods by selecting more...

Supplier Evaluation and Assessment How to Meet FDA QSR and ISO 13485 Requirements in a Cost-Effective Manner - Webinar by Global ...qualification and assessment is required in both the QSR regulations and ISO standards. Many companies spend a great deal of time and money in pursuit of compliance with this. Many companies can spend MUCH LESS time and money, and still be in control of their suppliers and in compliance with the regulations. This presentation will review the QSR and ISO requirements for supplier evaluation more...

Statistical Concepts of Process Validation - Webinar by GlobalCompliancePanel ...rameters and develop challenge points for the Operational Qualification (OQ) phase. The guidance explains the concepts of process capability showing the relationship between the process statistical characterization and the engineering specification transferred from design. Statistical Process Control (SPC) is an important technique in the Performance Qualification (PQ) phase of validation. The more...

Verification of Pharmacopeia Methods - Webinar by GlobalCompliancePanel ..., consistent and reliable analytical test methods. Method qualification of a method can be achieved in three ways: Validation, Verification (Compendial Methods) and Method Transfer (company methods). Lack of such documentation can result in warning letters from both the FDA and Health Canada. This webinar explains the reason and purpose of USP chapter and helps you to interpret what is required more...

Leadership in Manufacturing Contamination Control Webinar will be on March 18, 2010. Webinar will be presented by Teri C. Soli. The Microbiology Lab must take leadership in contamination control support for production because it is the hub of the necessary technical expertise. This broad manufacturing support role covers many areas, including routine raw material and product testing, disinfectant/ sanitant qualification, water and compressed more...

FDA Compliant HPLC Qualification and Performance Testing ...l brings a new webinar on the topic of FDA Compliant HPLC Qualification and Performance Testing. Webinar will be on March 4, 2010. Webinar will be presented by Dr. Ludwig Huber. Mr. Huber is Director of Lab compliance and Chief Advisor for global FDA compliance at Agilent Technologies. He is the editor of Lab compliance, the global on-line resource for validation and compliance issues for more...

From Coaches Plus

Coach Practitioner Course

...ecialises in awarding Coaching, Leadership and Management qualifications. ILM qualifications are highly valued, and last year 90, 000 people enhanced their leadership and management skills with an ILM qualification. This will give you access to all the resources and materials provided to ILM members to support your development. These include: * access to the Learning Zone an more...

From HOOD Group

HOOD CPRE E-Learning -Certified Professional for Requirements Engineering - Foundation Level

This unique E-Learning opportunity is an ideal way to prepare for the certification examination of the International Requirements Engineering Board. The online training course has been developed by experts in requirements management & engineering, who have been significantly involved in producing the syllabus and examination for the "Certified Professional for Requirements Engineering (CPRE)" more...

From PsyAsia International

Online Basic Psychometric Course

This is a very basic introductory course for those interested in psychometric tests at work. If you are looking for a qualification in psychometrics. This course runs over 5 weekly sessions, starting at 5. 45pm on Wednesdays. Each session lasts for 40 minutes and there is time after this for questions and discussion. The course is subsidised by PsyAsia, but there is a small fee of just US$3. 50 more...

From Procept Associates Limited

PRINCE2 Foundation and Practitioner

... As PRINCE2 ® is a very successful project management qualification, a large number of people and organisations have used and implemented PRINCE2. A number of case studies have been commissioned as examples of how successful PRINCE2 ® has become within their organisations. The full list can be downloaded here. PRINCE2 ® training is delivered in association with Raj Khanna more...

From Parenta Training

Childcare Level 2 Certificate

The Level 2 Certificate for the Children and Young Peoplea ™s Workforce is suitable for those who are employed in a childcare setting and have recently started their career in early years. It allows you to work with children under supervision and count in the staff ratios. The qualification develops your personal knowledge of childcare and the essential skills involved in working with more...

From cGMP UNIVERSITY INC

Principles of supplier Quality management A one hour webinar descriping principles governing supplier Quality management more...

From iGallant Solutions

ITIL V3 Foundation ...ement (CSI) ITIL ® Glossary publications ITIL ® Qualification Scheme and Awareness Our Special Features ITIL ® Exam Passing Warranty Online Live Instructor Training Self Paced e-Learning Mock Exams Mock Exam Mock Exam is designed similar to actual ITIL ® exam pattern. a 40 Questions a 60 minutes duration. a Passing Rate : 65%, 26 Out Of more...

From Olympus Training Ltd

Level 3 Certificate in Personal Training ...el 3 Certificate in Personal Training. The aim of this qualification is to recognise the skills, knowledge and competence required for an individual to work unsupervised as a personal trainer. This includes being able to offer one-to-one training, baseline assessment, nutritional advice and progressive programming which is specific to the individual needs of a client. Level 3 Personal more...

Level 2 Gym Instructor courses In many ways this is one of the landmark courses we deliver. This is because on completion it qualifies the candidate to work in a fitness suite as a gym instructor. It also allows people to move onto other specialisma ™s such as personal training and/ or class teaching. We deliver courses in Ipswich, Norwich, London, Liverpool, and Thetford. Level 2 Gym Instructor Courses cover: more...

From 4BS Solutions

webmethods 8 training

...ail to eai. architects@gmail. comPre Required Educational Qualification for Trainees Any graduate having some Knowledge on OOPS Concepts (Like C++) and Basic SQL commands Training Methodology @4BSInstructor led web class, Voice through Conference Calls, Presentation through Web Access (Desktop sharing), Training Coordinated by our Online Training Coordinator, A Batch size ranging between 4-10 more...

From Business Expert Webinars

Forecasting & Pipeline Management ...you'll learn: Why doing a great job of sales opportunity qualification is critical to forecast and pipeline accuracy How to inspect pipeline data quality Three common flaws that cause forecasting and pipeline management systems to fail Why 'valid next steps' are critical to sales opportunity pipeline accuracy How to design sales opportunity pipeline reports to maximize accuracy and more...

The Secret to Closing More Sales ...e quality of the work that is done during the OPPORTUNITY QUALIFICATION stage of the sales process that determines whether a sale will close, as well as how hard or easy it will be to close. Plus, when done correctly, the information gathered during sales opportunity qualification can be used to improve the effectiveness of your proposals and product demonstrations. During this webinar you more...