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Effective Quality Agreements in Regulated Industries
- Key Components of Quality Agreements: Understanding the essential elements that every quality agreement should include, such as roles, responsibilities, and quality oversight.
- Alignment with FDA Expectations: Learning how to structure agreements that meet FDA requirements and ensure regulatory compliance.
- Supplier Responsibilities and Communication: Defining clear lines of responsibility for suppliers and establishing effective communication channels to maintain quality standards.
- Monitoring and Auditing Supplier Compliance: Developing strategies for ongoing monitoring and conducting audits to verify supplier adherence to the agreement.
- Risk Management and Mitigation: Identifying potential risks in the supply chain and incorporating contractual terms to manage and mitigate these risks.
- Change Control and Documentation Requirements: Establishing procedures for managing changes to processes or products and maintaining proper documentation to support compliance and traceability.
Overview of the webinar
In FDA-regulated industries, quality agreements are vital tools for ensuring that manufacturers and their suppliers or contract organizations are aligned on quality and compliance expectations. These agreements help define the responsibilities of each party and outline the procedures for maintaining product quality throughout the supply chain. Without clear, well-structured agreements, companies risk regulatory violations, product recalls, or compromised safety. This training covers the key elements of effective quality agreements, focusing on how to align with FDA expectations, manage supplier compliance, and reduce risk through detailed contract terms. By understanding these critical components, companies can ensure smooth operations and safeguard their compliance with industry standards.
Who should attend?
- Quality Assurance Manager
- Regulatory Affairs Specialist
- Supplier Quality Engineer
- Compliance Officer
- Procurement Manager
- Operations Manager
Why should you attend?
Attending this training will provide valuable insights into the creation and management of effective quality agreements, which are essential for ensuring product quality and regulatory compliance in FDA-regulated industries. Participants will learn how to structure agreements that define clear roles and responsibilities, align with FDA expectations, and mitigate risks through strategic contract terms. This training is crucial for professionals seeking to enhance supplier oversight, minimize compliance risks, and safeguard their company’s reputation by ensuring that all parties in the supply chain maintain consistent quality standards.
Faculty - Miss.Meredith Crabtree
Meredith Crabtree has over 25 years’ experience in regulated industries ranging from Pharma, Medical Device, Biologics, Laboratory testing, Cosmetics, and Supplements. She has worked in both manufacturing and distribution as well as Human Health and Animal Health. Meredith currently works as a Quality Consultant performing label reviews, 3rd party inspections, Consent Decree and Recall support. She also performs regulatory assessments and Quality training. Meredith has a degree in Medical Technology and is currently obtaining a degree in Quality Systems.