Compliance4All to organize webinar on Process Validation Requirements & Compliance Strategies on July 17

Fremont, CA: Process Validation requirements and compliance strategies will be the topic of an hour-long webinar that Compliance4All, a leading provider of professional trainings for all the areas of regulatory compliance, is organizing on July 17. The learning objective this webinar has is to explain strategies for achieving a robust and reliable Process Validation that meets the latest FDA guidelines. For more on this webinar, please visit http://bit.ly/2JaknFv
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Process Validation is considered as the first step in process development for manufacturing biopharmaceuticals. PV can be of tremendous value in helping organizations to increase the reliability of a process, improve yields, and bring down operating expenses, but only when used as intended. How do companies achieve the right PV and meet Process Validation requirements that ensure these benefits? This is the learning that the participants of this webinar will get.

José Mora, who is a Principal Consultant specializing in Manufacturing Engineering and Quality Systems, will be the expert at this webinar. As one who has specialized in manufacturing, process development, tooling, and Quality Systems during the over 30 years he has worked in the medical device industry; José is the ideal person to explain how to implement the right compliance strategy policy and processes.

At this webinar, he will offer compliance strategies for achieving a process that is vigorous and consistent, and meet Process Validation protocols. He will explain the latest, relevant regulatory guidelines in this aspect. Participants of this webinar will walk away with the ability to evaluate the validation requirements for any given process.

Looking beyond compliance
José will emphasize validation basics. Yet, he will lead participants to think beyond compliance towards achieving a strong process. Towards facilitating this, he will cover the following areas at this webinar:
    Global Harmonization Task Force requirements (includes FDA and ISO)
    Installation Qualification (IQ)
    Operational Qualification (OQ)
    Performance Qualification (PQ)
    Design Qualification
    Facilities and utilities
    Strategies for achieving a robust and reliable process
    Typical process validation protocols.

This webinar on understanding PV requirements and adapting the right compliance strategies will be of immense benefit to personnel such as Managers, Supervisors, Directors, and Vice-Presidents in the areas of:
    Research & Development
    Quality Engineering
    Auditing
    Manufacturing    
    Quality Assurance & Quality Control
    Operations
    Document Control
    Device Development
    Verification and Validation Planning, Execution and Documentation for Devices.