GMP Data Integrity Expert Panel Discussion – LIVE free Webcast
GMP Data Integrity Expert Panel Discussion – Free Webcast
60-minute recording now available
“Add to Cart” for download
Areas For Discussion
Our Panel of Experts will discuss best practices for implementation, management and regulatory compliance of data integrity. They will answer questions and engage in comprehensive conversations on:
- 20+ common data integrity issues
- Recent regulatory changes; impact
- What regulators look for
- Detecting and preventing data integrity issues
- Part 11 compliance
For a free transcription of the entire webcast recording – click here
Read our recent blog post “What are the areas of greatest risk for data integrity issues?” – click here
Who Will Benefit
Industry professionals from many areas who may interact directly with regulatory inspectors or who help prepare for inspections, including:
- Quality Assurance/Quality Control
- IT Professionals
- Technical Operations
For Customer Care – Please Contact Us
Phone: (+1) 844.686.5750
Our Expert Panel Biographies
Dr. James Blackwell, MBA is The Founder, President and Principal Consultant of The Windshire Group. Dr. Blackwell has been a prominent industry consultant for over twelve years, working on a wide variety of CMC and quality issues for a broad range of companies, investors, and product types at all stages of the product life cycle. Prior to consulting, he held several senior positions in technical operations, manufacturing and process development at prominent operating companies.
Dr. Blackwell is trained as a scientist, engineer and businessman. He received his Ph.D. in Chemical Engineering from Northeastern University. He received his dual M.B.A./M.S. Technology Management from the University of Maryland, and graduated with B.S. Chemical Engineering and M.S. Microbiology degrees from The Ohio State University.
Alfonso C. Fuller is a consultant who specializes in quality system, software quality, regulatory, enforcement and compliance matters for FDA regulated medical device, pharmaceutical and biotech manufacturers, suppliers, importers and vendors. He has extensive experience in Part 11 (electronic signatures and records), document management systems and quality systems.
Having practiced in Washington, D.C., Mr. Fuller is highly experienced in communicating with FDA headquarters and field staff. He has worked on a number of consent decree and remediation-related projects. Mr. Fuller has specialized in regulated industry for 25+ years.
Danielle DeLucy is an industry veteran and specializes in the areas of Quality Assurance and Quality Systems as a consultant. Prior to this role, Danielle has been in the industry for 15 years serving in numerous quality management roles, such as the Director of Product Quality with oversight of sterility assurance practices and numerous filling and packaging operations. Danielle began her career as a Quality Control pharmaceutical microbiologist at a contract laboratory where she performed various tests for their clients. In the years after, she has held positions in the quality management arena with increasing responsibility. She has helped to lead many regulatory health inspections and was instrumental in the coaching process of her peers prior to any inspection. Currently, Danielle assists companies who: 1) are faced with warning letters and consent decrees; 2) wish to improve GxP practices; and 3) need to establish more robust quality systems.
Registrants may cancel up to two working days prior to an on-line course or webinar start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. On-site training can be cancelled up to ten business days prior to training. Windshire will be compensated for any travel cancellation fees. Courses and webinars may be cancelled due to unavoidable factors. Registrants will be notified if a cancellation occurs. Attendees can choose between the recorded (on-demand) version of the webinar or a full refund for any Windshire cancelled webcast.
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