This webinar will provide valuable guidance to regulated companies in development and implementation of Product Risk Management Planning, Implementation, and Use. There will be added focus on the special needs of combination products. Also increased focus on the often high risk considerations of drug delivery systems, with the recent increased concern posed by potential cybersecurity vulnerabilities. This webinar will expand this tool into R&D design control, training, marketing, validtion, root cause analysis, CAPA/fralure investigations, GMP auditing, and liability reduction. Regular use of a few simple but powerful tools in a Product Risk Management File and Review template can contribute greatly to reduction of product liability, company-wide cost reduction efforts, less chance of recalls, and an improved bottom line.
Why Should You Attend:
Both the U.S. FDA and the EU's MDR require product risk management as part of virtually all regulatory compliance efforts. Combination products can add to risk exponentially. And Drug Delivery Systems are many times extremely high risk, requiring even more complex analyhsis Companies must be proactive in reducing product risk .while increasing user benefits. Companies are still not developing the required tools nor using them in all regulated/CGMP activities, especially the newer expanded requirements of the 2019 version of ISO 14971, When used, companies have often not provided the full documentation to allay investigators'/auditors' concerns. Existing risk documents are not being used to their full potential.Areas Covered in the Webinar:
- Key requirements of ISO 14971 and ICH Q9
- The definition of 'risk' to avoid an automatic FDA Warning Letter
- Suggested Report formats to meet both US FDA and EU MDR requirements
- Expected sources of information for evaluation and inclusion
- How to compile
- A key member of the Risk Management Team
- When to involve the team
- How to complete, document and control as a 'living' document
- An often neglected safety feature
- QMS integration - a recent emphasis.
- Incorporation into the design and development (R&D) phase
Who Will Benefit:
This webinar will provide valuable assistance to all regulated companies that need a repeatable methodology, and their in-house personnel trained in cGMP and MDD/CE-marking compliance. It will discuss and provide examples of ISO- and FDA/D6ICH-compliant product risk management templates. This applies to companies in the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields. The employees who will benefit include:- Senior management
- Regulatory Affairs
- Quality Assurance
- Production
- R&D and Engineering
- All personnel tasked with product hazard reduction and problem solving
Course Provider
John E Lincoln,
