Inter Scientific

🎄 Wishing You a Merry Christmas from Inter Scientific! 🎄 As the holiday season approaches, we want to take a moment to thank all our clients, partners, and colleagues for a fantastic year of collaboration and success. Your trust and support drive everything we do, and we’re grateful to be part of your journey. This Christmas, we celebrate the spirit of innovation, teamwork, and the shared goal of making industries safer and more compliant. We look forward to continuing our work together in the new year, building on the progress we’ve achieved. From all of us at Inter Scientific, we wish you a joyful Christmas and a prosperous New Year! ✨ #MerryChristmas #HappyHolidays #InterScientific #ThankYou #SeasonGreetings

Navigating the complex regulatory landscape for medical devices can be challenging, but at Inter Scientific, we provide the expert guidance and support you need. Our team offers comprehensive solutions to help ensure your products achieve and maintain global compliance with precision and efficiency. From technical documentation and auditing to device lifecycle management and professional training, we offer tailored solutions to help you achieve and maintain regulatory readiness. Our services include: Technical Documentation: Ensuring compliance with ISO standards, UKCA/CE certification, and risk management. Auditing: Internal audits for EU MDR, UK MDR, and ISO 13485:2016 compliance. Device Lifecycle Management: Registration, coordination with Notified Bodies, and continuous monitoring for compliance. Professional Training: Empowering your team with knowledge on EU MDR, ISO 13485, and more. Whether you're looking to achieve certification, streamline your processes, or stay ahead of regulatory changes, we are here to help you succeed. Get in touch with us today to learn how we can support your medical device regulatory needs -https://ow.ly/v87e50Uw1LP #MedicalDeviceRegulation #MDR #ISO13485 #Compliance #RegulatoryAffairs #InterScientific #UKCA #CEMark #MedicalDevices #DeviceLifecycle #Training

On 17 December 2024, the Office for Product Safety and Standards (OPSS) published a new Statutory Instrument: ‘The Cosmetic Products (Restriction of Chemical Substances) (No. 2) Regulations 2024’. Key changes include: ✅ 64 CMR substances added to Annex II of the UK Cosmetics Regulation (UKCR). ✅ Kojic acid added to Annex III, restricted to 1% in face and hand products. The regulations come into effect on 31 January 2025, with deadlines for compliance throughout 2025 and 2026. 📖 For detailed information, read the full article here: https://lnkd.in/eYX4wUfg 📩 Need help with compliance? Contact us: https://lnkd.in/eD3928dB #CosmeticRegulations #Compliance #CMRSubstances #OPSS #KojicAcid #ProductSafety

🌟 Thank You, DDL 2024! We had an incredible time at Drug Delivery to the Lungs Conference (DDL) for pulmonary and nasal drug delivery! The event was a fantastic opportunity to connect with brilliant minds, explore cutting-edge innovations, and gain valuable insights into the future of inhalation medicine. A huge thank you to the organisers for creating such a well-organised and impactful forum for collaboration and learning. Special thanks to everyone who stopped by to speak with us – your engagement made this experience truly memorable! At Inter Scientific, we’re excited to continue supporting our partners with expert regulatory guidance and helping advance innovative therapies in the field of drug delivery. 🌐 Missed us at the conference? Reach out anytime via our website: https://ow.ly/mmEB50UtXYZ We’d love to hear from you! #DDL2024 #DrugDelivery #InhalationMedicine #RegulatorySupport #PulmonaryDrugDelivery

The Modernisation of Cosmetics Regulation Act (MoCRA) marks a significant milestone for the US cosmetic industry, introducing new requirements such as facility registration, product listing, fragrance allergen labelling, and Good Manufacturing Practices (GMP). With extended deadlines and proposed rules forthcoming, businesses must stay ahead to ensure compliance and uphold product safety. Discover the key changes, upcoming requirements, and how to prepare for this transformative legislation in our latest blog. Read more here: https://ow.ly/krhY50UtVRf #MoCRA #CosmeticCompliance #RegulatoryUpdates #FDA #InterScientific#CosmeticIndustryInsights

We are thrilled to announce that Inter Scientific will be attending Drug Delivery to the Lungs Conference (DDL) 2024, Europe’s premier conference for pulmonary and nasal drug delivery. This annual forum is a hub for innovation and collaboration, dedicated to advancing the development of medicines for inhalation. Representing our team will be David Lawson our Chief Executive; CINDY LEDUC, our Business Development Manager; and Daire Keyes, our Regulatory Specialist. The event promises to be an exciting platform for exploring cutting-edge solutions, discussing emerging trends, and fostering partnerships in the field of drug delivery. This year’s DDL Christmas Lectures format adds a festive and engaging touch to the learning and networking opportunities. If you’re attending, we’d love to connect! Let’s discuss how Inter Scientific’s expertise can help you navigate the complexities of regulatory pathways and bring innovative therapies to market efficiently and effectively. Reach out to us: https://ow.ly/XbRN50Uo472 #DDL2024 #DrugDelivery #InhalationMedicine #RegulatorySupport #PulmonaryDrugDelivery

We were delighted to attend the ECCC Annual Conference 2024, a cornerstone event for the vaping industry. This year, our Chief Executive, David Lawson, participated in the “Global Regulatory Trends” panel, offering valuable insights into the evolving compliance landscape and its impact on manufacturers worldwide. We’ve also enjoyed meeting clients and industry partners face-to-face, sharing how our advanced analytical services and regulatory expertise support the development of safer and compliant vape products. A big thank you to everyone who connected with us and engaged in meaningful discussions. If you couldn’t meet us at the event, feel free to reach out—we’d love to explore how we can support your compliance and product development needs. 👉 Reach out to us: https://ow.ly/8cM950UmopE #ECCC2024 #VapeIndustry #GlobalRegulations #ComplianceSolutions #VapeTesting #InterScientific

We’re excited to announce that Inter Scientific will be attending the ECCC Annual Conference 2024! This year’s conference will take place on 6th December 2024 at JW Marriot Hotel Bao’an Shenzhen, China. Our Chief Executive, David Lawson, will join the panel on “Global Regulatory Trends,” sharing valuable insights on navigating the evolving compliance landscape and its implications for manufacturers worldwide. Alongside David, our Technical Specialist (Nicotine Contained Products), Benjamin Green, will be on hand to engage with industry stakeholders and explore the latest innovations driving the future of the vape sector. We’re also looking forward to meeting clients and partners in person, fostering connections, and discussing how our advanced analytical services and regulatory expertise can support the development of safer, compliant vape products. Have questions or want to learn more? Reach out to us : https://ow.ly/ScJ450UkUsm #ECCC2024 #VapeIndustry #Compliance #VapeTesting #InterScientific

At Inter Scientific, we offer a full suite of vape analysis services designed to support industry compliance, product quality, and consumer safety. From nicotine content and carbonyl analysis to volatile organic compounds and heavy metal screening, our expert team ensures that each vape product meets necessary quality and safety requirements. Our services cover essential testing, including nicotine-related substances, flavour compounds, and extractables and leachables to help maintain consistency and regulatory alignment. With state-of-the-art technology and validated methods, we’re here to support your efforts in quality control and compliance. Connect with us to learn how our expertise can benefit your products and enhance consumer trust: https://ow.ly/uW5i50Uhllj #ProductTesting #QualityControl #SafetyStandards #Compliance #IndustryExcellence #ConsumerTrust

As the EU tightens regulations on cosmetic ingredients, manufacturers need to be aware of new restrictions and bans taking effect in 2025. From prohibitions on specific nano materials and endocrine disruptors to limits on popular ingredients like Vitamin A, Arbutin, and Retinol, these changes impact every phase of compliance planning. 🗓️ Upcoming Deadlines to keep on your radar: 1 February 2025: Deadline for placing products with restricted substances like Genistein and Daidzein on the EU market. 1 May 2025: Ban on 4-Methylbenzylidene Camphor in cosmetics. 31 December 2024 to 1 May 2027: Progressive deadlines for Triclocarban, Triclosan, and Homosalate compliance. Our latest blog breaks down these critical regulatory updates and provides insights to help you align your compliance strategy with EU standards. Don’t get caught unprepared – read the full post to understand how these changes affect your products and plan accordingly. 🔗 Read more here: https://ow.ly/q28G50UgCnT #Cosmetics #EUCosmeticsRegulation #Compliance #ProductSafety #CosmeticIngredients #RegulatoryUpdates #InterScientific