Did you miss our recent webinar "Keep your Manufacturing Secrets Confidential" with Melissa Sayers (Phillips) and Megan Moore? Discover the essentials of Master Files (MFs) in the drug industry by watching the recording on your own time. In this webinar we answer the following: -Overview of Master Files: Understanding the role and importance of MFs in the drug industry. -Agency Utilization: Detailed discussion on which agencies utilize MF submissions. -Required Documents: Common documentation requirements for MF submissions. -Fee Structures: Clarification on when fees apply for MF submissions. -Submission Processes: Step-by-step guide on MF submission processes. -eCTD Submissions: Introduction to the electronic Common Technical Document (eCTD) format for MFs. -Registrar Corp Solutions: How our solutions can streamline regulatory compliance and ensure data protection. Watch Now: https://hubs.li/Q02H7CR30 #RegistrarCorp #FreeWebinar #FDACompliance
Registrar Corp
Government Relations Services
Hampton, Virginia 6,713 followers
Registrar Corp assists companies with U.S. FDA Regulations
About us
Registrar Corp provides U.S. FDA registration, U.S. agent, and regulatory compliance assistance for U.S. and non-U.S. companies in the food and beverage, medical device, drug, cosmetics, and radiation-emitting device industries. Registrar Corp provides expert assistance in 19 different languages, 24 hours per day, 7 days per week. Registrar Corp was founded in 2003 to assist businesses with compliance with U.S. Food and Drug Administration (U.S. FDA) regulations. Since opening its headquarters in Hampton, Virginia, USA, Registrar Corp has expanded to nineteen international offices and has aided more than 20,000 companies across 150 countries. Employees include former U.S. FDA officials, scientists, and industry experts. Registrar Corp is not affiliated with the U.S. FDA.
- Website
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http://www.registrarcorp.com
External link for Registrar Corp
- Industry
- Government Relations Services
- Company size
- 51-200 employees
- Headquarters
- Hampton, Virginia
- Type
- Privately Held
- Founded
- 2003
- Specialties
- U.S. FDA Food, Beverage, and Dietary Supplement Regulations, U.S. FDA Drug Regulations, U.S. FDA Medical Device Regulations, U.S. Cosmetic Regulations, U.S. Agent Regulations, U.S. FDA Radiation-Emitting Electronic Device Regulations, and U.S. FDA Regulations
Locations
Employees at Registrar Corp
Updates
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🚨 Attention Cosmetic Companies! 🚨 As of July 1st, 2024, the FDA is enforcing MoCRA for all cosmetic companies. You must report and maintain records of all adverse events related to your products. Since the deadline has passed, we've heard of companies receiving a serious adverse event without a reporting solution in place. Remember, you only have 15 days to report adverse events after receiving a request from the FDA. Don't risk supply chain disruptions and costly penalties! We offer the first-of-its-kind Adverse Event Management (AEM) software to help you comply with MoCRA. Our software manages everything from intake to FDA reporting. 💻Consumer-Friendly Intake 📈Real Time Tracking & Monitoring 🔒Protect Medical/Personal Data 🏥FDA MedWatch-ready Get MoCRA compliant now with our AEM software: https://hubs.li/Q02H6KLr0 #RegistrarCorp #Cosmetics #MoCRA #FDACompliance #AdverseEventManagement
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Did you miss our recent webinar, Unwrapping FDA's MoCRA Labeling Regulations with Anna Benevente? Learn about the upcoming labeling requirements mandated by MoCRA as well as the general requirements all cosmetic products must meet by watching the recording on your own time. Anna describes in detail what must appear on your products’ labels and the timelines for compliance. Webinar recording: https://hubs.li/Q02G_fMw0 #RegistrarCorp #FreeWebinar #CosmeticsIndustry #MoCRA #MoCRACompliance
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Join us for our free webinar on August 14th, 2024 at 1PM ET with GLP experts Jaclyn M Bellomo, MBA and Cynthia Weber who will take you through an introduction of the requirements of 21 CFR 58, Good Laboratory Practices for Nonclinical Studies and give you valuable examples of why GLP is important in a lab setting while identifying if the regulation applies to you and your company. They will also give you key strategies for implementation and how to maintain compliance. 🌟Understanding of GLP and the specific requirements of 21 CFR 58 🔍Recognize the importance of GLP 💡Know when and if the regulations apply to your cosmetics laboratory Register Now: https://lnkd.in/gKTn2QJA #RegistrarCorp #FDACompliance #FreeWebinar
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Last year 51% of U.S. food importers audited by the FDA failed - mainly due to an inadequate Foreign Supplier Verification Program (FSVP). Businesses that don’t comply with complicated FSVP regulations are putting themselves at risk of costly penalties and supply chain disruptions. Join us for our free webinar on August 21st, 2024 at 1PM ET with FSVP compliance experts Coley Anderson and John Kelly to discover the new requirements of the FSVP Final Guidance, common challenges that U.S. importers currently face, tools to automate and simplify FSVP compliance and how to stay audit-ready 24/7. Register Now: https://lnkd.in/dihZANCA #RegistrarCorp #FDACompliance #FreeWebinar
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🚨1 week left until Cosmoprof North America, July 23-25, 2024🚨 Come and meet our knowledgeable staff at booth 18244!🎉 Do you have questions on the newest FDA and MoCRA Cosmetic requirements? Schedule a meeting with Coley Anderson and learn how you can: 📋Prepare your cosmetics for MoCRA's new requirements, including facility registration and product listing 📝Get assistance modifying your cosmetics labels to stay compliant as government regulations change 📈Keep your team updated as U.S. FDA implements additional MoCRA guidelines https://hubs.li/Q02FWdfP0
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Only 2 weeks left until the NCBFAA Educational Institute (NEI) will be hosting its 10th Annual Global Trade Educational Conference, July 28-30, 2024. Are you going to be attending the event? Schedule a meeting with our FDA and MoCRA expert, Coley Anderson and learn about: 📋Challenges with Facility Registration/Product Listing Requirements 📝Implementing new Adverse Event Requirements for Cosmetics 📈Recent FDA Rulemaking and Upcoming Requirements https://hubs.li/Q02G6n050 #RegistrarCorp #FDACompliance #RegulatoryAffairs #FoodSafety #Cosmetics
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Only 2 weeks left until Cosmoprof North America, July 23-25, 2024. We are thrilled to be a part of this event and will be located at booth 18244!🎉 Schedule a meeting with our Cosmetics FDA and MoCRA expert, Coley Anderson and learn how you can: 📋Prepare your cosmetics for MoCRA's new requirements, including facility registration and product listing 📝Get assistance modifying your cosmetics labels to stay compliant as government regulations change 📈Keep your team updated as U.S. FDA implements additional MoCRA guidelines https://hubs.li/Q02FVN_R0
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🚨 Attention Cosmetic Businesses! 🚨 📅 TODAY is the deadline (July 1, 2024) to submit your facility registrations and product listings to the FDA, as required by the FDA Modernization of Cosmetics Regulation Act of 2022 (MoCRA). U.S. retailers are demanding MoCRA compliance from their suppliers. Without proof of compliance, you risk being removed from their stores. Need help meeting the FDA’s deadline? Become MoCRA compliant today: https://lnkd.in/gsTkD77D #MoCRA #Compliance #Cosmetics #FDA
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The NCBFAA Educational Institute (NEI) is hosting its 10th Annual Global Trade Educational Conference which will give customs brokers, freight forwarders, NVOCCs, OTI, service providers, importers, exporters and all global logistics professionals an opportunity to update themselves on industry developments and connect with colleagues. Are you going to be attending the event? Schedule a meeting to learn how Registrar Corp can assist you with staying updated on FSVP best practices for importers and we can answer your specific questions regarding FDA regulations: https://lnkd.in/gyyYeUqx Registrar Corp will be represented by Anna Benevente and Coley Anderson. #RegistrarCorp #FDACompliance #RegulatoryAffairs #FoodSafety #Cosmetics
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