Cosmetics GMP – Be prepared for US MoCRA

In this webinar, we will delve into the essential principles of GMP and explore how the US FDA’s Modernization of Cosmetics Regulatory Act (MoCRA) could elevate your manufacturing operations to new heights of compliance and efficiency.

In today's rapidly evolving regulatory landscape, staying ahead of the curve is more crucial than ever. With the increasing complexity of cosmetics manufacturing, organizations face many challenges in ensuring product quality, safety, and regulatory compliance. A robust GMP framework based on ISO 22716 offers a comprehensive platform that enables companies to build a quality system, thereby navigating these challenges imposed by MoCRA with confidence and precision.

Throughout the webinar, we will discuss the key components of cosmetics GMP to demonstrate how organizations can align themselves to mitigate risks, streamline change management processes, and assure product quality throughout the manufacturing lifecycle. Whether you're a seasoned professional or new to GMP compliance, this webinar will equip you with practical insights and strategies to optimize your operations and maintain a competitive edge in the market, driving sustainable success in today's regulatory environment.

Objective

The learning objective of this webinar is to raise awareness and:

1. Understand the essential principles of Good Manufacturing Practices (GMP) and their significance in the cosmetics industry.
2. Explore the US Modernization of Cosmetics Regulatory Act (MoCRA) and its implications for cosmetics manufacturers regarding compliance and efficiency.
3. Recognize the challenges cosmetics manufacturers face in ensuring product quality, safety, and regulatory compliance in today's rapidly evolving regulatory landscape.
4. Gain insights into the GMP framework, particularly ISO 22716, and its role in helping organizations build a robust quality system to navigate regulatory challenges imposed by MoCRA.
5. Identify GMP's key components and relevance in mitigating risks, streamlining change management processes, and ensuring product quality throughout the cosmetics manufacturing lifecycle.
6. Learn practical strategies and best practices for aligning with GMP principles to optimize operations and maintain a competitive edge in the cosmetics market.
7. Acquire knowledge applicable to seasoned professionals and newcomers to GMP compliance, empowering attendees to enhance their understanding and implementation of GMP standards.
8. Explore how adherence to GMP principles can drive sustainable success for cosmetics manufacturers in today's regulatory environment.These learning objectives aim to provide attendees with a comprehensive understanding of GMP principles, and their practical implications for cosmetics manufacturing operations. They also emphasize the importance of staying updated on regulatory requirements and leveraging GMP frameworks to achieve compliance and efficiency goals.

Agenda

• Understanding the intent of GMP Principles specifically concerning ISO 22716
• Brief comparison between ISO 22716 and Regulatory GMP
• Defining GMP in the cosmetics supply chain
• Explore MoCRA and its implications for cosmetics manufacturers regarding compliance and efficiency
• The benefits of adopting a GMP framework within your organization
• Key items in quality and five pillars of GMP
• Leveraging GMP Frameworks for Compliance and Efficiency
• Practical Insights and Best Practices: Documentation, Records, Buildings & Facilities, Equipment, Personnel, Raw Materials, Production, Laboratory Controls, Internal Audits, Complaints, Adverse Events, and Recalls
• Q&A

Target Audience:

• Cosmetics Manufacturing Professionals: Quality Assurance Managers, Regulatory Affairs Specialists, Production Managers, Compliance Officers, Manufacturing Engineers
• Cosmetics Industry Consultants: Regulatory Consultants, Quality Management Consultants, Compliance Advisors
• Small to Medium-Sized Cosmetics Manufacturers: Owners/Entrepreneurs, Start-up Founders, Managers of Small Manufacturing Facilities
• Cosmetics Industry Professionals Seeking Continuous Education: Professionals interested in staying updated on GMP principles and regulatory requirements. Individuals responsible for ensuring compliance and quality in cosmetics manufacturing
• Academic and Research Institutions: Faculty Members, Researchers, Students pursuing degrees in Cosmetic Science, Regulatory Affairs, Quality Management, or related fields
• Government Regulatory Agencies: Inspectors, Regulatory Officials involved in overseeing cosmetics manufacturing compliance
• Cosmetics Industry Associations and Trade Organizations: Representatives from industry associations focused on cosmetics manufacturing standards and regulations

Language: English

Cost: No Charge

Can't make a live session? Register now and receive a complimentary recording after the live event.

Speakers:

Jon Gawlak

Technical Manager/Senior Auditor, SGS North America

Over 30 years of Quality and Project Management Experience with over 25 years of Leadership Experience in the Pharmaceutical, Cosmetic, Personal Care, Food, and Medical Device Industry

Specialties: QA, QC, Supplier Qualification and Management, CMC, Quality Management, Project Management, Certification Auditing, Vendor Auditing, Internal Auditing, Analytical Testing, QC Laboratory Management

John Armstrong

Regional Sales Manager, Pharmaceuticals, SGS North America

John has over twenty years of experience in the healthcare industry holding senior leadership roles in commercial operations, sales and sales training with a focus on biopharmaceuticals, medical devices and OTC skin care products.

Currently, John is a Regional Sales Manager at SGS covering the Eastern USA for Pharmaceutical Products.

For further information, please contact:

Dominic James
Marketing Assistant
t: +1-862-339-6737