Inter Scientific

14/10/2025

💫 𝐈𝐧𝐭𝐞𝐫 𝐒𝐜𝐢𝐞𝐧𝐭𝐢𝐟𝐢𝐜 𝐚𝐭 𝐭𝐡𝐞 𝐈𝐧𝐡𝐚𝐥𝐚𝐭𝐢𝐨𝐧 𝐚𝐧𝐝 𝐑𝐞𝐬𝐩𝐢𝐫𝐚𝐭𝐨𝐫𝐲 𝐃𝐫𝐮𝐠 𝐃𝐞𝐥𝐢𝐯𝐞𝐫𝐲 𝐂𝐨𝐧𝐟𝐞𝐫𝐞𝐧𝐜𝐞!

Inter Scientific had a successful time at the 6th Annual Inhalation and Respiratory Drug Delivery Conference! It was a pleasure connecting with so many experts and innovators to discuss the latest developments in inhalation science, device technology, and regulatory trends shaping the future of respiratory drug delivery.

A big thank you to the organisers and everyone who stopped by to share insights and ideas - events like this truly highlight the collaboration driving progress in our industry.

At Inter Scientific, we remain committed to supporting the development of safe, effective, and compliant inhalation products, from early-stage formulation through to market readiness.

💡 If you’d like to continue the conversation or learn more about our work in inhalation research, we’d love to hear from you!

13/10/2025

🌱 𝗦𝘂𝘀𝘁𝗮𝗶𝗻𝗮𝗯𝗶𝗹𝗶𝘁𝘆 & 𝗖𝗼𝗺𝗽𝗹𝗶𝗮𝗻𝗰𝗲 𝗶𝗻 𝗖𝗼𝘀𝗺𝗲𝘁𝗶𝗰𝘀 🌍

Cosmetic manufacturers face growing pressure to demonstrate sustainability and compliance, and the EU Ecolabel is becoming a key standard in this journey.

As a recognised mark of environmental excellence, the EU Ecolabel applies to both rinse-off and leave-on cosmetics. Its criteria include:

🌱 Biodegradable ingredients
🚫 Restricted hazardous substances
📦 Sustainable packaging
✅ Proven performance

With the current criteria valid until 31 December 2027, now is the right time for manufacturers to align their products and processes.

✅ In our latest blog, we break down:
What the EU Ecolabel means for cosmetics
The key compliance criteria
Steps to apply successfully

Read more here: https://inter-scientific.com/eu-ecolabel-for-cosmetics/

10/10/2025

Today on World Mental Health Day, we reaffirm our commitment to fostering a culture where wellbeing comes first.

Supporting mental health isn’t a one-day event - it’s an ongoing responsibility we all share.

With the support of our Mental Health First Aider and our wider team, we’re continuing to build a workplace that is compassionate, balanced, and human. 💚

08/10/2025

💫 𝐏𝐚𝐫𝐭𝐢𝐜𝐢𝐩𝐚𝐭𝐢𝐨𝐧 𝐢𝐧 𝐭𝐡𝐞 𝐈𝐧𝐡𝐚𝐥𝐚𝐭𝐢𝐨𝐧 𝐚𝐧𝐝 𝐑𝐞𝐬𝐩𝐢𝐫𝐚𝐭𝐨𝐫𝐲 𝐃𝐫𝐮𝐠 𝐃𝐞𝐥𝐢𝐯𝐞𝐫𝐲 𝐂𝐨𝐧𝐟𝐞𝐫𝐞𝐧𝐜𝐞!

We’re excited to announce our participation in the 6th Annual Inhalation and Respiratory Drug Delivery Conference!

We’re looking forward to connecting with experts and innovators in the field to discuss the latest advances in inhalation science, device technology, and regulatory trends shaping the future of respiratory drug delivery.

At Inter Scientific, we’re dedicated to supporting the development of safe, effective, and compliant inhalation products, from early-stage formulation to market readiness.

💡 If you’re looking for targeted support for your inhalation research, don’t hesitate to reach out.

📅 9th-10th October
📍Barcelona

&Y International

07/10/2025

𝐏𝐚𝐫𝐭𝐢𝐜𝐢𝐩𝐚𝐭𝐢𝐨𝐧 𝐢𝐧 𝐭𝐡𝐞 𝐨𝐩𝐞𝐧𝐢𝐧𝐠 𝐜𝐞𝐫𝐞𝐦𝐨𝐧𝐲 𝐨𝐟 𝐌𝐚𝐝𝐫𝐢𝐝 𝐇𝐞𝐚𝐥𝐭𝐡 𝐇𝐮𝐛 🎉

Inter Scientific had the pleasure of participating in the opening ceremony of Madrid Health Hub. This initiative represents a great step forward in fostering innovation, collaboration, and digital transformation in the healthcare sector.

At Inter scientific, we are proud to contribute with our expertise in analytical, regulatory, and testing services, supporting the development of safer and more reliable health solutions.

We look forward to collaborating with the ecosystem at Madrid Health Hub and continuing to drive progress together.

19/06/2025

🌟 𝐏𝐫𝐨𝐮𝐝 𝐆𝐨𝐥𝐝 𝐒𝐩𝐨𝐧𝐬𝐨𝐫 – 𝐑𝐄𝐒𝐂𝐎𝐍 𝐏𝐚𝐫𝐢𝐬 𝟐𝟎𝟐𝟓 🇫🇷

June 17–18 | Respiratory Drug Delivery & Medical Devices

We were proud to take part as Gold Sponsor at RESCON 2025 in Paris, a key industry event focused on respiratory and drug delivery devices.

It was a pleasure to connect with innovative companies and thought leaders across the sector, and to share how we support the development and compliance of inhalation and combination products through our regulatory and analytical services.

A big thank you to the organisers for an excellent event, and to everyone who visited our booth!

📩 If you're working on a respiratory or drug delivery product and need regulatory or testing support, don’t hesitate to reach out!

30/04/2025

🔍 Check Out Our Latest Blog: Mastering Clinical Evaluation & Documentation for EU MDR Compliance

Clinical evaluation and documentation are no longer formalities under EU MDR 2017/745 — they’re essential to your device’s market access and ongoing compliance.

With stricter requirements for clinical evidence and reduced reliance on legacy equivalence, manufacturers must build a robust, defensible body of evidence to prove safety and performance.

✅ Key Insights:
🔹 Understanding the 5-step clinical evaluation process under MDR
🔹 Creating and maintaining your Clinical Evaluation Plan (CEP) and Report (CER)
🔹 Aligning clinical activities with PMS, PMCF, and risk management documentation
🔹 Embedding clinical evaluation into your QMS for lifecycle compliance

Whether you're launching a new device or updating existing documentation, this guide helps you meet MDR expectations with confidence and clarity.

📖 Read more: https://inter-scientific.com/mastering-clinical-evaluation-and-documentation-for-mdr-compliance/

Navigating the European Union’s Medical Device Regulation (MDR 2017/745) is a complex task for manufacturers, particularly when it comes to clinical evaluation and documentation. These processes are no longer optional formalities, they’re essential pillars of compliance that directly affect a de...

25/04/2025

𝐍𝐞𝐞𝐝 𝐇𝐞𝐥𝐩 𝐰𝐢𝐭𝐡 𝐕𝐚𝐩𝐞 𝐂𝐨𝐦𝐩𝐥𝐢𝐚𝐧𝐜𝐞? 𝐖𝐞'𝐯𝐞 𝐆𝐨𝐭 𝐘𝐨𝐮 𝐂𝐨𝐯𝐞𝐫𝐞𝐝 𝐚𝐭 𝐖𝐕𝐒 𝐃𝐮𝐛𝐚𝐢!

🚨 Inter Scientific is proud to partner with Dubai to deliver the 𝐅𝐈𝐑𝐒𝐓-𝐄𝐕𝐄𝐑 𝐂𝐨𝐦𝐩𝐥𝐢𝐚𝐧𝐜𝐞 𝐂𝐥𝐢𝐧𝐢𝐜 - a major industry-first offering expert regulatory support to v**e manufacturers, brands, and distributors 🚨

As the v**e industry continues to grow, so do the rules that shape it. From shifting global standards to strict local regulations, the path forward can feel like a maze. 🔦

That’s where the Compliance Clinic comes in. Think of it as your personal regulatory compass - built to help professionals navigate the complex, ever-changing world of compliance with confidence.

Inside this dedicated space, our experts will be on hand to offer one-on-one sessions on:

✅ UK TRPR Compliance
✅ EU TPD Compliance �
✅ US PMTA Advice �
✅ Product Testing & Safety �
✅ Regulatory Strategy & Documentation

Whether you’re launching a new product or expanding into new markets, this is your chance to get the answers you need from the people who know.

We are here to help you 😊

Exhibitors can pre-book appointments, securing time with specialists before the show begins.
https://allintheloop.com/events/world-v**e-show-2025/

📅 18-20 Jun 2025
📍 World V**e Show- Dubai

And for visitors, walk-up sessions will be available during show day, because we know that sometimes, the best questions are the ones you didn’t know you had until you got there.

At the World V**e Show Dubai, we’re not just celebrating the industry - we’re helping it grow smarter, safer, and stronger.

**eShow **eCompliance **eIndustry
**eShow **eCompliance **eIndustry

23/04/2025

🔍 How Usability Impacts Your EU MDR Strategy

Medical devices must not only perform, but they must also be safe, effective, and intuitive for the end-user.

In this post, we break down how usability engineering is no longer optional under the EU MDR. It’s a must-have for demonstrating safety and performance throughout the product lifecycle.

📊 Swipe through to explore:
✅ Key usability requirements in MDR
✅ How usability impacts risk management
✅ Tips for aligning usability with your Technical Documentation
✅ Common obstacles to avoid

🛠 Whether you're updating your existing device or launching a new one, usability must be integrated from the start.

💬 Take a look and let us know how is your team approaching usability under EU MDR?

16/04/2025

🔍 Check Out Our Latest Blog: Navigating Risk Management Under EU MDR

Risk management isn’t just best practice - it’s a legal obligation under EU MDR 2017/745. With stricter regulatory expectations and the need to align with ISO 14971, manufacturers must take a proactive, lifecycle-wide approach to risk.

✅ Key Insights:
🔹 Integrating risk management across the entire product lifecycle
🔹 Applying ISO 14971 principles to meet EU MDR requirements
🔹 Understanding and applying “state of the art” practices
🔹 Keeping your Risk Management File continuously updated with real-world data

Whether you're preparing for a PMA or improving your QMS, this blog provides a practical guide to staying compliant and ensuring patient safety.

📖 Read more: https://inter-scientific.com/navigating-risk-management-under-eu-mdr/

In the highly regulated world of medical devices, risk management isn’t just a best practice, it’s a legal necessity. With the introduction of the European Union Medical Device Regulation (EU MDR 2017/745), manufacturers are facing stricter expectations regarding how they assess and manage...