Ensuring Compliance with Inspectors virtual, sheridan

OVERVIEW
Attending this training will help the participants understand the specific requirements and expectations of FDA inspectors, allowing them to develop SOPs that meet regulatory standards and demonstrate compliance. By learning how to write SOPs that satisfy FDA inspectors, participants can proactively identify and address potential compliance gaps or issues. This training will provide them with the knowledge and skills necessary to develop robust and comprehensive SOPs, minimizing the risk of regulatory non-compliance and associated penalties.

WHY SHOULD YOU ATTEND?
Formal and documented Standard Operating Procedures (SOPs) serve as the cornerstone for effective operational practices. Within the realm of FDA audits, it’s noteworthy that SOP inadequacies rank among the top 5 findings. Furthermore, nearly every shortfall pinpointed in the FDA’s 483s and Warning Letters can be linked back to an organization’s deficient or non-existent SOPs.

This training program is designed to elucidate common errors and advocate best practices, helping organizations convey that their processes are comprehensive, precise, and consistently adhered to.

LEARNING OBJECTIVES
Attend the webinar to know why written procedures and beneficial and understand the FDA expectations for regulatory requirements and written documents.

AREAS COVERED
Understand the purpose and significance of Standard Operating Procedures (SOPs) in regulatory compliance.
Learn the key components of effective SOPs.
Gain insights into the structure and format of SOPs that satisfy inspectors and auditors.
Explore best practices for writing clear and concise SOPs.
Identify common mistakes to avoid when drafting SOPs.
Enhance your ability to create SOPs that meet industry standards and regulatory requirements.

WHO WILL BENEFIT
The following professionals will benefit from this training:

Managers
Supervisors, and lead workers in Regulatory Affairs
Quality Assurance and Quality Control personnel
Quality systems specialists
Document control specialists
CAPA specialists and managers
Regulatory and compliance specialists
Internal auditors and managers
Training specialists and managers

About speaker
Meredith Crabtree has over 25 years of experience in regulated industries, ranging from Blood, Plasma, Tissue, Laboratory, Pharma, Medical Devices, Cosmetics, Supplements, and Animal Health manufacturing and distribution. Meredith 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.