“Computer Software Assurance for Manufacturing, Operations, and Quality System Software

  Рет қаралды 14,230

Pharma Best Practices Webinars

Pharma Best Practices Webinars

Күн бұрын

In this webinar hear directly from the “FDA/industry CSA Team member”, featuring industry experts, who will conduct a panel discussion, about the upcoming draft Computer Software Assurance (CSA) draft guidance from FDA’s CDRH division. The guidance covers the principles of risk-based CSA, provide FDA’s perspective, and share numerous real-life success stories and their resulting value.
ISPE GAMP® global leadership strongly supports this risk- and quality-based approach to the assurance of computerized systems and believes that current ISPE GAMP® guidance is already fully aligned and consistent with such an approach, including new guidance coming this year from the CDRH.
About the Panel
Khaled Moussally - EVP, Clients & Regulatory Relationships - Compliance Group Inc.- Khaled Moussally has 25+ years of experience in the Life Sciences industry and is a well-known and well-respected thought leader on Quality & Compliance. Khaled is a key member of the FDA Case for Quality / "FDA CSV Industry Team", a contributing author to to the upcoming FDA guidance on Computer Software Assurance (CSA) and a contributing ISPE GAMP member to the Appendix of the Good Documentation Guidance on Data Integrity.
Stephen Cook - VP, Quality and Computer Software Assurance - Compliance Group Inc.
Stephen Cook has 20+ years of experience in the field of computer systems validation and is an expert on FDA’s upcoming guidance on Computer Software Assurance (CSA)
Harsha Chulki: Head of Global IT Quality, Compliance & CSV - ICU Medical Inc.-Harsha is responsible for ensuring high quality and compliant solutions are developed and deployed by ICU Medical's Global IT organization. A key player in the transition of regulated systems.
Sachin Bhandari Chairman, ISPE, Steering Committee Member - GAMP India CoP. Experienced professional in Pharmaceutical and healthcare compliance domain with wide experience in GXP, 21 CFR part 11, GAMP 5 and other compliance requirements and adherence.

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