Registrar Corp

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Registrar Corp Trusted partner to help you navigate global regulatory requirements.

ISO 27001 certified and serving over 30,000 clients in over 200 countries across the food and beverage, medical device, drug, and cosmetics industries. Founded in 2003, Registrar Corp is your trusted partner helping you navigate global regulatory requirements with expert services, innovative software solutions and comprehensive online compliance training to minimize business risk and avoid costly disruptions. ISO 27001 certified and serving over 30,000 clients in over 200 countries across the food and beverage, medical device, drug and cosmetics industries, Registrar is the most trusted leader in the industry. We provide expert assistance in 19 regional offices globally, 24 hours per day, 7 days per week. Contact Registrar Corp:
Phone: +1-757-224-0177
Fax: +1-757-224-0179
Email: [email protected]
Website: www.registrarcorp.com
24/7 Live Help: www.registrarcorp.com/livehelp

AI can generate training content quickly, but food manufacturers still need courses that are interactive, trackable, con...
10/22/2026

AI can generate training content quickly, but food manufacturers still need courses that are interactive, trackable, consistent, and ready to use in an LMS.

That’s where SkillUp AI Create comes in.

SkillUp AI Create helps organizations turn SOPs, work instructions, PDFs, and other existing materials into structured eLearning courses that can be assigned, tracked, and managed within the training platform.

For food manufacturers, that means less time spent building courses from scratch and more consistency across workforce training.

Read the full article:
https://hubs.li/Q04C0YzJ0

Explore SkillUp AI Create:
https://hubs.li/Q04C0Yy40

Compare how standard AI tools like ChatGPT & Claude stack up against purpose-built AI course creator tools. Learn how AI LMS platform aids AI course creation.

Thank you to everyone who joined our webinar, Labelling & Regulatory Requirements in FDA OTC Monograph. Watch on demand ...
10/21/2026

Thank you to everyone who joined our webinar, Labelling & Regulatory Requirements in FDA OTC Monograph. Watch on demand now: https://hubs.li/Q04BV9c60

During the session, Joyce Rivera-Santiago shared practical insight into FDA expectations for OTC drug products, including formulation considerations, labeling requirements, claims, and the Drug Facts panel.

Attendees learned more about:
• FDA OTC monograph requirements
• Reviewing OTC product formulations
• General OTC labeling requirements
• Structuring the Drug Facts panel
• Addressing common compliance challenges before entering the U.S. market

Need help with OTC drug labeling or regulatory compliance? Contact Registrar Corp: https://hubs.li/Q04BV9c-0

Stay ahead of changing cosmetics regulatory requirements and strengthen your team with Registrar Corp’s upcoming webinar...
10/21/2026

Stay ahead of changing cosmetics regulatory requirements and strengthen your team with Registrar Corp’s upcoming webinar:

💄 Cosmetics | English
📅 November 17, 2026 | 2:00–3:00 PM Manila Time
Export Your Cosmetics: One Hour to Understand Regulatory Challenges Across the USA, UK/EU, and Canada
🎤 Presenter: Vijey Ananda

Explore key regulatory differences across major cosmetics markets and learn what to consider when preparing products for international expansion.
🔗 Register: https://hubs.ly/Q04BTRgv0

Can’t make it to the webinar? Our regulatory experts are still here to help.

Contact us to discuss your compliance questions: https://hubs.ly/Q04BTRfS0

10/20/2026

ETIQUETADO Y REQUISITOS REGULATORIOS EN LAS MONOGRAFÍAS DE LA FDA PARA PRODUCTOS OTC

Un panel de Información del medicamento o “Drug Facts” que cumpla con la normativa de FDA es fundamental, pero es solo una parte de la evaluación de un medicamento OTC o de venta libre. La formulación, el uso previsto, las declaraciones y otros datos que figuran en la etiqueta también deben ser adecuados conforme a la monografía aplicable de la FDA.

Acompáñenos mañana 20 de Octubre en nuestro WEBINAR gratuito: Requisitos de etiquetado y regulación en las monografías de medicamentos OTC de la FDA, donde analizaremos de manera práctica cómo se relacionan dichos elementos, cuáles son los problemas de cumplimiento normativo más frecuentes y qué aspectos deben revisarse antes de comercializar un producto OTC en el mercado estadounidense.

¡Traiga sus preguntas para la sesión de preguntas y respuestas en vivo!

Fecha: martes, 20 de octubre de 2026.
Hora: de 08:00 a. m. a 09:00 a. m., hora de Guatemala

Ponente: Joyce M. Rivera Santiago. Especialista Senior en revisión de productos, etiquetado e ingredientes de Registrar Corp.

Regístrese solicitando el enlace a nuestro correo [email protected], o a nuestra página de Facebook.

Si no puede asistir, regístrese y le enviaremos la grabación.

Pregunte por otros servicios FDA para Alimentos, Bebidas, Cosméticos, Medicamentos y Dispositivos Médicos.

Tel: +502 2300-1803 | WhatsApp: +502 3043-8652

Registrar Corp

📍 Upcoming October EventsRegistrar Corp will be connecting with industry professionals around the world this October acr...
10/20/2026

📍 Upcoming October Events
Registrar Corp will be connecting with industry professionals around the world this October across industries If you’ll be attending, we’d love to connect.

🍴 SIAL Paris
📅 October 17–21
📍 Paris, France
Visit our team at Hall 7, Booth G445 to discuss food compliance, labeling, and global market access.
🔗 Schedule a meeting with Michelle Sheriff:
https://hubs.li/Q04BL8fC0

🍴 Food Safety Consortium
📅 October 21–23
📍 Washington, DC
Meet Coley Anderson to discuss food safety and regulatory compliance.

🏥 CMEF Beijing
📅 October 21–24
📍 Beijing, China
Registrar Corp will be attending this major medical device event.

🌎 Southern Border Conference
📅 October 25–28
📍 Laredo, Texas
Meet Coley Anderson to discuss import, customs, and regulatory compliance.

🍴 TechniCAL’s Thermal Processing Course
📅 October 27–30
📍 New Orleans, Louisiana
Join TechniCAL for hands-on training in thermal processing, scheduled processes, FDA filings, retort systems, and deviation evaluation.

🌎 SupplySide Global
📅 October 28–30
📍 Las Vegas, Nevada
Meet Coley Anderson to discuss compliance and market access across regulated industries.

Can’t make it to an event? Connect with Registrar Corp to discuss your compliance needs: https://hubs.li/Q04BL87k0

10/19/2026

CUMPLIMIENTO FDA DE FACTORES CRITICOS EN UN PRODUCTO ACIDIFICADO

Si el pH de equilibrio final de un producto acidificado es superior al pH de equilibrio presentado a la FDA en el proceso programado o archivo de proceso (Scheduled Process/SID), esto se considera una desviación, incluso si el pH de equilibrio final es inferior a 4.6.

El incumplimiento de cualquier otro factor crítico especificado en el proceso programado/SID también es considerado por la FDA como una desviación.

El equipo de especialistas de puede ayudarle a determinar si su producto se considera un alimento acidificado o de baja acidez, ayudar con el registro FCE o “Food Canning Establishment” requerido por la FDA, proporcionar asesoría para determinar los parámetros a incluir en los archivos de proceso correspondientes o SIDs y en la presentación de los mismos.

Obtenga información sobre estos requisitos y nuestros servicios enhttps://www.registrarcorp.com/resources/free-tools/fce-wizard/

Pregunte por otros servicios FDA para Alimentos, Bebidas, Cosméticos, Medicamentos y Dispositivos Médicos.
Tel: +502 2300-1803 | WhatsApp: +502 3043-8652
Email: [email protected]

Registrar Corp

10/19/2026

WEBINAR GRATUITO: ETIQUETADO Y REQUISITOS REGULATORIOS EN LAS MONOGRAFÍAS DE LA FDA PARA PRODUCTOS OTC

Los productos farmacéuticos de venta libre (OTC) comercializados en EE.UU. deben cumplir con requisitos específicos de las monografías de la FDA en cuanto a formulación, etiquetado, declaraciones y el panel de información del medicamento (Drug Facts). El incumplimiento de estos requisitos puede ocasionar detenciones en aduana, retrasos y costos inesperados antes de que un producto llegue al mercado.

En este WEBINAR GRATUITO se brindará información práctica sobre las expectativas de la FDA respecto a las monografías para productos OTC y los factores de cumplimiento que las empresas deben considerar para estos productos.

Los temas incluirán:
• Descripción general de los requisitos de las monografías de la FDA para productos OTC
• Aspectos que deben considerarse al revisar las formulaciones de productos OTC
• Requisitos generales de etiquetado para productos farmacéuticos OTC
• Cómo abordar el panel de información del medicamento (Drug Facts)
• Orientación práctica para abordar los desafíos comunes de incumplimiento relacionados con las monografías para productos OTC

Fecha: 20 de Octubre, 2026
Hora: 08:00 a 9:00 a.m hora de Guatemala

Regístrese solicitando el enlace a nuestro correo [email protected], o a nuestra página de Facebook.

Si no puede asistir, regístrese y le enviaremos la grabación.

Pregunte por nuestros servicios FDA para Alimentos, Bebidas, Cosméticos, Medicamentos y Dispositivos Médicos.

Tel: +502 2300-1803 | WhatsApp: +502 3043-8652

Registrar Corp

Every safe bite is the result of work most people never see: a documented food-safety plan, an accurate label, a supplie...
10/16/2026

Every safe bite is the result of work most people never see: a documented food-safety plan, an accurate label, a supplier check done right. This World Food Day, we're recognizing the quality and regulatory teams who make 'safe and nutritious food for all' more than a phrase. Thank you for the standards you hold.

Registrar Corp helps food and beverage companies navigate food safety, labeling, supplier verification, and regulatory requirements so they can confidently bring their products to market. Explore how we can help: https://hubs.li/Q04BpFJn0

Thank you to everyone who joined How to Use AI to Improve Workforce Training!During the webinar, Chris Bell demonstrated...
10/15/2026

Thank you to everyone who joined How to Use AI to Improve Workforce Training!

During the webinar, Chris Bell demonstrated SkillUp AI Create and showed how organizations can use AI to turn existing training materials into interactive, LMS-ready eLearning courses.

Attendees saw how SkillUp AI Create can help:
• Accelerate course development
• Convert SOPs, PDFs, and PowerPoints into training
• Generate quizzes and voiceovers
• Streamline review and publishing
• Support scalable, audit-ready workforce training

Missed the live session or want to see the demo again? Watch the webinar on demand and learn how SkillUp AI Create can help your organization build high-quality training faster.

🎥 Watch on demand: https://hubs.li/Q04BgS0G0

Want to explore SkillUp for your workforce? Contact Registrar Corp: https://hubs.li/Q04BgSgb0

Want to see what better training could look like?For a limited time, you can try SkillUp Workforce Training Platform fre...
10/15/2026

Want to see what better training could look like?

For a limited time, you can try SkillUp Workforce Training Platform free for 2 weeks.

Use the free trial to:
• Compare SkillUp’s course library to your current training materials
• Test how easy it is to assign, track, and report on training
• Explore SkillUp course creation for custom training development
See how SkillUp can help simplify training management and support a stronger, more consistent workforce training program.

Start your 2-week free trial: https://hubs.li/Q04BgJs90

Address

144 Research Drive
Hampton, VA
23666

Opening Hours

Monday 7am - 6pm
Tuesday 7am - 6pm
Wednesday 7am - 6pm
Thursday 7am - 6pm
Friday 7am - 6pm

Telephone

(757) 224-0177

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