* Has this verification process been validated by a security professional?* Has this verification process been approved by your auditors and/or the insurer that covers your fidelity guarantee risk?Validation of these facilities, processes, and process controls is possible using historical data to provide the necessary documentary evidence that the process is doing what it is believed to do.Dear Birmingham City Council, In terms of the Freedom of Information Act of 2000, could you please provide me with information on how you ensure that ratepayers are who they say they are when they contact you to transact on their accounts.Twelve 2-day In-person Interactive GMP and Validation Seminars available in America, Europe and Asia delivered by Dr. Understanding the Final FDA Guidance for Validation of Analytical Methods With 10 best practice guides for easy implementation Recorded, available at any time Analytical Instrument Qualification According the new Revision of USP Effective Validation of Analytical Methods for GLP and Clinical Studies Learn how to design, prepare, conduct and document for FDA Compliance Recorded, available at any time Impact of Quality by Design on the Analytical Laboratory Learn through examples on development and validation of analytical procedures Recorded, available at any time Quality by Design (Qb D) for Analytical Method Development and Validation Learn how to design robustness for easy transfer and to avoid OOS situations Recorded, available at any time Recorded, available at any time Eight Steps for Cost-effective Laboratory Compliance Up-to-date overview, hot topics and trends. Method validation is the process used to confirm that the analytical procedure employed for a specific test is suitable for its intended use.Recorded, available at any time Verification of Compendial Methods according to the New USP Chapter Understand the new risk based approach and and get real world case studies for testing Recorded, available at any time Effective HPLC Method Development and Validation Preparation, conduct and documentation for FDA/EMA Compliance Recorded, available at any time Recorded, available at any time Development and Validation of Stability Indicating Methods for FDA/ICH Compliance Sample generation - method development - validation - documentation Recorded, available at any time Bioanalytical Method Validation Conduct and Document for Efficiency and FDA and EMEA compliance Recorded, available at any time Residual Solvent Analysis According to USP Recorded, available at any time System Suitability Testing in Compendial Chromatographic Methods Understanding and Implementing Recent Changes of USP and EP Recorded, available at any time With compliance master plan, checklists, examples, audio seminar and 31 SOPs for easy implementation Click here for more info The Laboratory compliance package includes 31 SOPs. The package includes 50 FDA and international regulations and guidelines Here Ludwig Huber (right) in the Q&A Discussion Session on Laboratory Compliance at a ISPE/FDA Beijing University Conference with Nick Buhay, Acting Director in FDA/CDER's Division of Manufacturing and Product Quality A large portion of this tutorial comes from the book: Validation and qualification in Analytical Laboratories, published by Informa in 2007. Results from method validation can be used to judge the quality, reliability and consistency of analytical results; it is an integral part of any good analytical practice.
More specifically, please provide the following information on your verification process for securely validating ratepayer identity before they transact on their accounts (where transactions can be anything from updating their bank details, to requesting refunds): * What information (be it proof of identity, account numbers, specific transaction details) do you require from ratepayers to validate that they are the person they claim to be, and – in the case of commercial ratepayer accounts – authorised to transact on that account?
Note that I am not requesting any personally-identifying information, only the process itself.
Process validation is defined as the collection and evaluation of data, from the process design stage throughout production, which establishes scientific evidence that a process is capable of consistently delivering quality products.
Process validation is a requirement of current Good Manufacturing Practices (GMPs) for finished pharmaceuticals (21CFR 211) and of the GMP regulations for medical devices (21 CFR 820) and therefore applies to the manufacture of both drug products and medical devices. Food and Drug Administration (FDA) has proposed guidelines with the following definition for process validation: – “PROCESS VALIDATION” is establishing documented evidence which provides a high degree of assurance that a specific process consistently produces a product meeting its predetermined specifications and quality attributes.
Process validation involves a series of activities taking place over the lifecycle of the product and process. Stage 1 – Process Design: The commercial process is defined during this stage based on knowledge gained through development and scale-up activities.