As we conclude RAPS Convergence 2024, we proudly reflect on an impactful final day. Our CEO, Suren Dheenadayalan, delivered a compelling presentation on “𝐑𝐞𝐝𝐞𝐟𝐢𝐧𝐢𝐧𝐠 𝐑𝐞𝐠𝐮𝐥𝐚𝐭𝐨𝐫𝐲 𝐀𝐟𝐟𝐚𝐢𝐫𝐬 𝐰𝐢𝐭𝐡 𝐇𝐮𝐦𝐚𝐧 𝐄𝐱𝐩𝐞𝐫𝐭𝐢𝐬𝐞 𝐚𝐧𝐝 𝐀𝐈-𝐏𝐨𝐰𝐞𝐫𝐞𝐝 𝐈𝐧𝐧𝐨𝐯𝐚𝐭𝐢𝐨𝐧” to a packed audience. The level of engagement and insightful discussions that followed truly underscored the importance of innovation in Regulatory Affairs. We want to extend our heartfelt thanks to everyone who attended our sessions, visited our booth, and engaged with us. Your collaboration and shared expertise made this event truly memorable As we wrap up our final day and prepare to move forward, we are excited about the future and look forward to further collaboration with Industry leaders. Here are a few visual highlights from our concluding day. Feel free to 𝐂𝐨𝐧𝐭𝐚𝐜𝐭 𝐔𝐬 if you want to know more about how Freyr can support you in your Regulatory journey. https://lnkd.in/guXYJHz5 #RAPSConvergence2024 #RegulatoryAffairs #FreyaFusion #Innovation #AI #LifeSciences #FreyrSolutions
Freyr Solutions
IT Services and IT Consulting
Princeton, New Jersey 69,203 followers
The Largest, Global, Regulatory Solutions and Services Provider.
About us
Freyr Solutions is the largest global, Regulatory solutions and services company that offers end-to-end Regulatory solutions to life sciences industries. The services include Regulatory affairs, pharmacovigilance, clinical research, quality management, and technology solutions such as Regulatory information management systems and Regulatory data integration. Freyr's expertise in Regulatory affairs makes it a trusted partner for life sciences companies seeking to navigate the complex Regulatory landscape. Our Vision “To be the essential partner to manage global Regulatory complexity and market safe and compliant products in local countries.” In order to succeed, we must first believe that we can, and we strongly believe the future is not something we enter, it is something we create. And we are here to create a compliant pathway for our customers’ global market entry. Quick Facts • 1600+ global customers and growing. • 2100+ in-house Regulatory experts. • 12+ years of a strong foothold in the Regulatory industry. • Have a presence across 20 global locations. • 850+ in-country Regulatory affiliates across 120+ countries. • ISO 9001 and ISO 27001 certified.
- Website
-
https://bit.ly/FreyrSolutionsWebsite
External link for Freyr Solutions
- Industry
- IT Services and IT Consulting
- Company size
- 1,001-5,000 employees
- Headquarters
- Princeton, New Jersey
- Type
- Privately Held
- Founded
- 2011
- Specialties
- Regulatory Affairs Services, Regulatory Affairs Consultant, CMC Regulatory Affairs, Pharmaceutical Regulatory Affairs, Medical Device Regulatory Affairs, Cosmetics Regulatory Affairs, Food Regulatory Affairs, Chemical Regulatory Affairs, Regulatory Publishing, Regulatory Submission, Regulatory Labeling, Artwork Management System, Pharmacovigilance Services, Pharmacovigilance Consultant, Regulatory Intelligence, Regulatory Strategy, Medical Writing, Regulatory Medical Writing, Regulatory Compliance Management, and Regulatory Compliance Management Software
Locations
Employees at Freyr Solutions
-
Rukmini Umanath
Sr. Vice President at Freyr Solutions
-
Serge Calet
-
Sugato Chanda
Leadership | Strategy | Transformation | Program Management | Account Management | Innovation | Developing and managing programs that support an…
-
Dr Ganesh Singh
Product Management/Solution Architect. Regulatory (RIMS, IDMP, xEVMPD, Publishing), Safety, Pharmacovigillance, DMS, HL7, Healthcare (HIMS), VEEVA…
Updates
-
❎ Don't let Regulatory data drive you mad; let it drive your decision-making instead! ✅ Are you also feeling overwhelmed and dismayed by having to go through heaps of never-ending Regulatory data, just to get that one critical insight? Let us take on your troubles! Let us introduce you to Freyr’s Regulatory Analytics Dashboards. 📊 🌐 📈 ⬇ Watch our video below to know more about our completely configurable, interactive and visually rich Regulatory dashboards called Freya.RACs! ➡ Book a demo now to experience Regulatory data visualization like never before: https://hubs.la/Q02NY7pY0 #Regulatoryintelligence #Regulatoryaffairs #Regulatorycompliance #AIinRegulatory #FreyrSolutions #FreyrGRI #Regulatorydashboards #globalregulatoryintelligence
-
𝐖𝐄𝐁𝐈𝐍𝐀𝐑 𝐈𝐍𝐕𝐈𝐓𝐄! Would you like to gain comprehensive insights on the Chinese medical device Regulatory landscape? Register for Freyr’s exclusive webinar on “𝐔𝐧𝐥𝐨𝐜𝐤𝐢𝐧𝐠 𝐂𝐡𝐢𝐧𝐚'𝐬 𝐒𝐚𝐌𝐃 𝐌𝐚𝐫𝐤𝐞𝐭: 𝐑𝐞𝐠𝐮𝐥𝐚𝐭𝐨𝐫𝐲 𝐏𝐚𝐭𝐡𝐰𝐚𝐲𝐬 𝐚𝐧𝐝 𝐂𝐡𝐚𝐥𝐥𝐞𝐧𝐠𝐞𝐬” scheduled for 𝐎𝐜𝐭𝐨𝐛𝐞𝐫 𝟑𝟎𝐭𝐡, 2024. https://lnkd.in/dDikQbqr #MedicalDevices #NMPA #RegulatoryMarket #AMR #EU #RoW #RegulatoryAffairs #FreyrSolutions #Webinar
-
Join us on October 17, 2024, for a comprehensive webinar titled "𝐔𝐧𝐝𝐞𝐫𝐬𝐭𝐚𝐧𝐝𝐢𝐧𝐠 𝐄𝐧𝐝-𝐭𝐨-𝐄𝐧𝐝 𝐂𝐨𝐬𝐦𝐞𝐭𝐢𝐜 𝐑𝐞𝐠𝐮𝐥𝐚𝐭𝐢𝐨𝐧𝐬 𝐢𝐧 𝐓𝐡𝐚𝐢𝐥𝐚𝐧𝐝." Gain valuable insights into the regulatory framework and ensure your compliance with key requirements. 🔹 Date: October 17, 2024 🔹 Topic: Understanding End-to-End Cosmetic Regulations in Thailand 🔹 Register Now to secure your spot! https://lnkd.in/ddwrxgCp #Cosmetics #Thailand #Regulations #Webinar #Compliance #RegisterNow #FreyrSolutions
-
𝐖𝐄𝐁𝐈𝐍𝐀𝐑 𝐈𝐍𝐕𝐈𝐓𝐄! Would you like to gain comprehensive insights on the Chinese medical device Regulatory landscape? Register for Freyr’s exclusive webinar on “𝐔𝐧𝐥𝐨𝐜𝐤𝐢𝐧𝐠 𝐂𝐡𝐢𝐧𝐚'𝐬 𝐒𝐚𝐌𝐃 𝐌𝐚𝐫𝐤𝐞𝐭: 𝐑𝐞𝐠𝐮𝐥𝐚𝐭𝐨𝐫𝐲 𝐏𝐚𝐭𝐡𝐰𝐚𝐲𝐬 𝐚𝐧𝐝 𝐂𝐡𝐚𝐥𝐥𝐞𝐧𝐠𝐞𝐬” scheduled for 𝐎𝐜𝐭𝐨𝐛𝐞𝐫 𝟑𝟎𝐭𝐡, 𝟐𝟎𝟐𝟒, for AMR, EU, and RoW regions. https://lnkd.in/gUCwiMNZ #MedicalDevices #NMPA #RegulatoryMarket #AMR #EU #RoW #RegulatoryAffairs #FreyrSolutions #Webinar
This content isn’t available here
Access this content and more in the LinkedIn app
-
Regulatory submissions entail a thorough process, demanding a nuanced grasp of distinct product categories, diverse regulatory prerequisites, and ever-changing guidelines. Despite this complexity, several misconceptions persist about regulatory submissions. #RegulatoryAffairs #RegulatorySubmissions #Pharmaceuticals #RegulatoryCompliance #FreyrSolutions #FreyrDigital
This content isn’t available here
Access this content and more in the LinkedIn app
-
Tired of manually comparing lengthy Regulatory documents? With Freya, it's never been easier! Simply ask Freya to analyze your documents, and it will quickly highlight what's unchanged and what's different. What's more? Get a detailed change summary in no time and focus on what really matters! Say goodbye to the hassle of document comparisons—Freya’s got you covered. To see Freya in action, Click here: https://lnkd.in/d4v2QdHn #AI #DocumentManagement #RegulatoryTech #Regulatoryintelligence #Regulatorycompliance #Regulatoryaffairs #AIInRegulatory #globalregulatoryintelligence #FreyrSolutions #FreyrGRI
-
The US FDA issued updated guidance on providing Regulatory submissions in the electronic format for certain human pharmaceutical product applications. This guidance outlines the organization and submission requirements using the eCTD specifications. The latest version was released on September 20, 2024, and aims to streamline the submission process for applicants. Consult Freyr for compliance with new updates. https://lnkd.in/gjtPYEAB #USFDA #RegulatorySubmissions #eCTD #SubmissionProcess #FreyrSolutions #PharmaReg
-
UPCOMING WEBINAR! Explore the latest on ePI FHIR labeling for a seamless transition. Join us for a webinar on ‘𝐞𝐏𝐈 𝐅𝐇𝐈𝐑 𝐋𝐚𝐛𝐞𝐥𝐢𝐧𝐠: 𝐔𝐧𝐝𝐞𝐫𝐬𝐭𝐚𝐧𝐝𝐢𝐧𝐠 𝐭𝐡𝐞 𝐈𝐦𝐩𝐨𝐫𝐭𝐚𝐧𝐜𝐞, 𝐆𝐮𝐢𝐝𝐞𝐥𝐢𝐧𝐞𝐬, 𝐚𝐧𝐝 𝐂𝐡𝐚𝐥𝐥𝐞𝐧𝐠𝐞𝐬,’ scheduled for 𝐍𝐨𝐯𝐞𝐦𝐛𝐞𝐫 𝟔, 𝟐𝟎𝟐𝟒. Register now. https://lnkd.in/gg5ang66 #Pharmaceuticals #ePIFHIRLabeling #Guidelines #Challenges #FreyrSolutions #FWS
This content isn’t available here
Access this content and more in the LinkedIn app
-
The US FDA released guidance - Amendments to Abbreviated New Drug Applications Under GDUFA - in September 2024. It explains amendment classifications, categories, and how submissions may affect assessment goal dates. The guidance establishes new performance goals and program enhancements for the generic drug assessment program. Freyr can help you with the complex ANDA amendment process and ensure timely approvals. Contact us for compliance. https://lnkd.in/gjtPYEAB #USFDAGuidance #ANDASubmissions #TimelyApprovals #PharmaReg #RegulatoryCompliance #FreyrSolutions