Yesterday was a busy day meeting with my U.S food importers, distributors and retailers. Everyone is doing their best to Comply with FSVP. But even my smartest of colleagues are struggling. Today's words of wisdom... organize, centralize and automate. Registrar Corp can help you do this. I meet with U.S importers and we FSVP level-set. What are you ACTUALLY doing in your FSVP Program? Do you monitor your supply chain for FDA violations? Do you monitor your FSVP importer DUNS number for misuse. If you are struggling with FSVP or you know someone struggling with FSVP, message me. Let's talk FSVP BEST PRACTICES. https://lnkd.in/evaCqr3X
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🔔 #ComplianceTuesday | September 24 🔔 Topic: General Product Safety Regulation (#GPSR) We’re nearing the big transition date, December 14, when the #GPSD officially turns into #GPSR. For this session, we’ll provide a brief overview of the key points and focus on an engaging #QandA session to answer your burning questions. If there are any last-minute updates, we’ll share them, but the spotlight is on you and your questions! 📅 Date: September 24 - Zoom Session 🕒 Time: 10h00 - 11h00 (Amsterdam-Time) 👉 Register here: https://lnkd.in/eTaEqnj Don’t miss this chance to get your questions answered before the transition! #ProductCompliance #Regulations #EUCompliance #SafetyStandards #GPSD #GPSR https://lnkd.in/eTaEqnj
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Marketing Analyst@ Acquis Compliance ❖ Marketing Strategy Development ❖ Social Media Management ❖ Content Creation ❖ SEO ❖ Digital Marketing Professional
If you’re placing products on the EU market, SCIP compliance is mandatory for all articles containing SVHCs (Substances of Very High Concern). Wondering how to get started! Swipe left to know more about SCIP compliance 👉 #SCIPCompliance #Sustainability #SupplyChain #EURegulations #HazardousSubstances #SVHC #Compliance
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With FSMA 204 less than 20 months out, the clock is ticking- now is the time to start your path to compliance . FSMA 204 compliance may seem overwhelming at first, but you're not alone. Visit https://lnkd.in/gDQUgeGV and leverage our 20+ years of traceability expertise!
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With the January 1, 2025 deadline for Poison Centre Notification (PCN) submissions under the EU CLP Regulation fast approaching, businesses have a crucial task at hand. It's not just about ensuring submissions are thorough and complete—it's also about diligently maintaining and updating them as necessary. Whether you're navigating your first submission or managing existing dossiers, mastering the timing and process of updating a PCN submission is key to staying compliant. Our team has addressed some of your most common questions to help you navigate the PCN submission process. Click here to learn more: https://lnkd.in/gBNixayy #PoisonCentreNotification #EUCompliance #RegulatoryGuidance #ChemicalSafety #HazCom #PCNDeadline #HazardCommunications
Updating Poison Centre Notification (PCN) Submissions: Requirements and Obligations — Yordas Group
yordasgroup.com
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Meet the speakers of #DaywithDISA 2024! Dan Horvath, Vice President of Safety Policy, will be presenting a session titled Safety and Regulatory Update with ATA. ⚖ This session will include insight into FMCSA's current regulatory actions, projections for regulatory developments in 2024, and strategies for staying updated and compliant with evolving regulations. ⌚ All sessions will be under one hour in length. ➡FREE Registration: https://zurl.co/OzXt #BackgroundScreening #FMCSA #Compliance
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Mastering Regulatory Compliance with the Care Notes blog The Care Quality Commission (CQC) plays a central role in setting the standards and guidelines. Read more here: https://zurl.co/Olfc
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Stay ahead of FSMA compliance! 📝 Dive deep into our latest blog where we break down the intricacies of PCP Preventive Control Plans. Confused? Don't navigate alone, let us help you with FSMA compliance https://rfr.bz/la0ol7f 🌐💡 #FSMA #PCP #FoodSafety" https://rfr.bz/la0ol7g 𝗦𝗵𝗮𝗿𝗲 𝗶𝗳 𝘆𝗼𝘂 𝗳𝗼𝘂𝗻𝗱 𝘁𝗵𝗶𝘀 𝘃𝗮𝗹𝘂𝗮𝗯𝗹𝗲! #usfsmaplan #pcpplanhelp
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Experienced Leader in Quality Systems Implementation & Management (CMQ/OE, CMDA, RAC-US, CMIIC)
Another unofficial trend observation with FDA Warning Letters; looks like they're getting tired of lots of back and forth with recipients who don't seem to get the nuances of FDA's concerns, so now they're being very specific about what actions they expect. I think this is a good thing, as it's better for public safety when companies implement the appropriate corrective actions more quickly rather than just applying band-aids (corrections). #QRxPartners #FDA #WarningLetters #InadequateResponse #MLV
🖋 In this week's Inadequate Response Series ... Remember when the FDA Warning Letters left it up to the recipient to determine what actions to take in response to the observed violations? Of course, the problem with that is that the Warning Letter is often a response to an inadequate response to a Form 483 Inspectional Observations, so why would the recipient be likely to provide an improved response the second time around? 🤔 Often, Warning Letters recommend engaging expert consultants, but a new trend we've noticed, and mentioned before, is the FDA using more forceful wording to make this an edict rather than a suggestion. The FDA also started stating more clearly what kind of actions they expected. However, in this week's Warning Letter, the FDA stepped up its game by providing very detailed lists of the actions required in the next response. Maybe this was because the recipient was a foreign manufacturer who might not fully understand the nuances of the regulations. 👉 Or maybe, and hopefully, the FDA realizes that since Warning Letters represent risks to public safety, being more clear increases the probability of the recipient taking meaningful action. However, even with this more clear approach, there continues to be a need to read between the lines and fully understand how best to meet the stated expectations. As the FDA now almost always suggests, get expert help like that available from QRx Partners. Make us your partner in quality and regulatory success! 🤝 Full FDA Warning Letter Here 👉 https://lnkd.in/gCfgP732 #QRxPartners #QRxInforms #mlv #InadequateResponse #WarningLetters #fdacompliance #quality #experts #consultants #fda #inspections #foreignmanufacturing #regulatorycompliance
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Preventive action can make a big difference in costly recalls and ensuring your device meets the quality standards that matter most to you. DPDC can help you be proactive rather than always having to be reactive. Give us a call to see how we can serve you. 804-965-3981 DPinfo@dpdconline.com #ClientIssues #PreventiveAction #QualityAssurance #ProfessionalInsights #CAPA #medicaldevice #regulatorycompliance #DPDC
Join us behind the scenes as we tackle critical client issues at Chicago O'Hare! Our latest video unpacks the intricacies of an internal audit and management review for a valued client. Discover how we addressed foreign matter issues with suppliers and took proactive steps to ensure airtight compliance. Watch as we send preventive action letters to suppliers, urging them to verify environmental conditions. Why? Because when the FDA arrives with our client, we want to showcase our proactive approach. Learn valuable insights into integrating preventive action into your CAPA system. It's not just compliance; it's about looking good doing it. Hit follow button for more updates! For more information visit our website dpdconline.com #ClientIssues #PreventiveAction #QualityAssurance #ProfessionalInsights #LinkedInExclusive #CAPA #doingthingsdifferently #compliance
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The deadline for compliance with the CIRMP rules in August 2024 may seem distant, but the journey to compliance is intricate and time sensitive. Take a tour of our product with one of our staff members and learn how Industrial Defender can ensure compliance with regulatory requirements. Learn more: https://hubs.li/Q02f2QGq0
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