As a Computer Validation Manager, the expert focuses on validation of computer systems in regulated environments, data integrity, and GMP compliance in pharmaceutical companies. In addition, Sinan Sahin focuses on developing (global) validation frameworks, providing CSV training, conducting CSV and IT supplier audits and regular reviews. In this context, besides his extensive range of experience and knowledge, he also draws on the numerous regulatory knowledge gained from the regulatory frameworks. Additionally, the scope of his projects includes international IT projects and IT system implementations. Sinan Sahin consults the pharmaceutical, chemical, and medical device industries on the qualification and validation of computerized systems and equipment.
Events/Masterclasses Sinan Sahin / Guest Speaker is currently speaking at
Pharma
Artificial Intelligence & Cloud: Validation and Data Integrity in a BioPharma GxP Environment
Online Live Stream
This course is a compilation of topics representing recent challenges related to CSV of AI or cloud-based systems in a GxP regulated context, and how CSV relates to data integrity.
Computerized Systems Validation, Data Integrity & Cloud Computing in Pharma & Biotech
Online Live Stream
This course is a compilation of topics representing recent challenges related to CSV of cloud-based systems in GxP regulated context, and how CSV relates to data integrity assurance.
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As a Computer Validation Manager, the expert focuses on validation of computer systems in regulated environments, data integrity, and GMP compliance in pharmaceutical companies. In addition, Sinan Sahin focuses on developing (global) validation frameworks, providing CSV training, conducting CSV and IT supplier audits and regular reviews. In this context, besides his extensive range of experience and knowledge, he also draws on the numerous regulatory knowledge gained from the regulatory frameworks. Additionally, the scope of his projects includes international IT projects and IT system implementations. Sinan Sahin consults the pharmaceutical, chemical, and medical device industries on the qualification and validation of computerized systems and equipment.
