Overview
Are you concerned about maintaining product quality and meeting stringent regulatory requirements in the rapidly evolving pharma and biotech industries? The complexity of these fields, along with the increasing demand for safety and compliance, has made the role of validation specialists more crucial than ever before.
Join our expert-led webinar to understand better the importance of validation specialists in ensuring product quality, safety, and regulatory compliance. Our webinar will provide valuable insights into the challenges faced by validation professionals and equip you with effective solutions to streamline your validation processes.
By attending this webinar, you will learn how validation specialists reduce the risk of costly recalls, minimise product development delays, and drive overall business success. Additionally, you will be able to interact with like-minded professionals and expand your network.
Don’t miss this unique opportunity to stay up-to-date with the latest validation strategies and techniques in the pharma and biotech industries. Register now and gain the knowledge and skills necessary to elevate your career and ensure your organisation’s success.
Speakers
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Nathan RomanHealthcare Consultant | Project ManagementOver the last 22 years I’ve placed thousands of temperature sensors in hundreds of control temperature chambers. Building on that experience, I’m continuously improving my efficient processes for faster delivery of fully qualified chambers for use. My name is Nathan Roman, and I have a passion to help others. I help people in the Health & Life Science industry learn how to implement and carry out temperature mapping studies and equipment qualifications (IQ, OQ, PQ).
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Thomas O'DonnellValidation SpecialistThomas O’Donnell is an entrepreneur and business owner with 20+ years of experience in the Pharmaceutical and Biotech industries with expertise in CQV.
As a dedicated leader in the Healthcare and Life Sciences industry, he has honed his skills in building start-ups, project management, facilitation, coordination, and team-building, supporting professionals in highly-regulated fields like Pharmaceutical and Biotech.
He is passionate about helping professionals learn about commissioning, qualification, validation, implementing EOS Worldwide, and business development.
Throughout his career, he has collaborated with renowned clients and stakeholders, effectively coordinating activities for the seamless execution of commissioning, qualification, and validation processes and maintaining the highest regulatory compliance standards.
Partner
Qualio
Website
https://qualio.com/Founded in 2012, Qualio is the first cloud quality management software for all Life Sciences companies. Medical device and pharmaceutical companies need a secure and scalable quality management system with the flexibility to support their evolving needs. Qualio meets that challenge by cutting through the complexity to optimize and automate critical quality processes. The remote-first, Qualio team is distributed across North America and Europe.
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Who Should Attend:
- Professionals in the pharmaceutical and biotech industries, such as validation specialists, quality assurance personnel, regulatory affairs experts, R&D scientists, process engineers, and management staff, want to understand the importance of validation in their respective fields.
- Skill Level: Intermediate , Expert
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Topics:
- Introduction to the importance of validation specialists in pharma and biotech.
- Key responsibilities of validation specialists.
- Regulatory requirements and compliance in validation.
- Best practices and recent trends in validation processes.
- Case studies: Successful validation projects in pharma and biotech.
- Interactive Q&A session.
- Networking and discussion opportunities.
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Special event information:
- All participants will get a complimentary certificate of attendance courtesy of the webinar's sponsor - Qualio.
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If you attend the live session you will get a digital certificate of attendance emailed to you within 7-working days.
Yes, our event partners will email you the event recording within several weeks.
