On-demand Webinars | Freyr - Global Regulatory Solutions and Services Company

Upcoming Webinars

Pharmaceuticals
Navigating eCTD Submissions in China
September 28, 2023
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Cosmetics
Understanding End-to-end Cosmetic Regulations in Japan
September 27, 2023
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Past Webinars

Food and Food Supplements
Demystifying Botanical Ingredients: An In-depth Outlook of Europe
September 13, 2023
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Medical Devices
Understanding RDC 751: A Comprehensive Analysis of its Impact on Medical Device Regulations
August 16, 2023
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Cosmetics
EU Cosmetic Ingredient Regulations: Exploring the Latest Legislative Updates and Future Restrictions
August 23, 2023
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Food and Food Supplements
Market Entry for Food Products and Supplements in Latin America: Navigating Regulatory Challenges
August 30, 2023
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Cosmetics
Decode the Cosmetic Regulatory Framework of the UAE
July 26, 2023
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Pharmaceuticals
Regulatory Perspective of Complementary Medicines in Australia
July 27, 2023
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Medical Devices
Mastering the Art of Periodic Safety Update Reports (PSURs)
July 19, 2023
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Cosmetics
Understanding the Cosmetic Regulatory Landscape of Mexico
June 29, 2023
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Freyr Digital
Paperless Thailand: Exploring the Future of eCTD Submissions
June 28, 2023
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Food and Food Supplements
Dietary Supplements Market Entry in China
June 27, 2023
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Medical Devices
Designing Operation Manuals for Medical Devices
June 07, 2023
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Food and Food Supplements
Food and Dietary Supplements Market Entry Challenges and Solutions - Japan
May 30, 2023
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Creating compliant packaging for a cosmetic product is a collaborative effort of various departments in an organization such as: Labeling, Artwork and Regulatory Affairs. While label artwork must be validated by an artwork labeling team, it must combinedly be reviewed and approved by Regulatory Affairs team to ensure the compliance.

Artwork services for the current Consumer Healthcare/Food Supplements landscapes are divided as per the markets. For Compliance based markets, artworks are created by Freyr team and submitted to the client for finalizing the artwork/ label.

The current medical device landscape has turned challenging for manufacturers in terms of ensuring quality and audit compliance due to ever-evolving regulations which may lead to extended time for approvals and market access.

Upcoming Webinars

Navigating eCTD Submissions in China

Understanding End-to-end Cosmetic Regulations in Japan

Past Webinars

Demystifying Botanical Ingredients: An In-depth Outlook of Europe

Understanding RDC 751: A Comprehensive Analysis of its Impact on Medical Device Regulations

EU Cosmetic Ingredient Regulations: Exploring the Latest Legislative Updates and Future Restrictions

Market Entry for Food Products and Supplements in Latin America: Navigating Regulatory Challenges

Decode the Cosmetic Regulatory Framework of the UAE

Regulatory Perspective of Complementary Medicines in Australia

Mastering the Art of Periodic Safety Update Reports (PSURs)

Understanding the Cosmetic Regulatory Landscape of Mexico

Paperless Thailand: Exploring the Future of eCTD Submissions

Dietary Supplements Market Entry in China

Designing Operation Manuals for Medical Devices

Food and Dietary Supplements Market Entry Challenges and Solutions - Japan

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