Freyr Solutions

Freyr Solutions One of the Largest, Global, Regulatory-focused Solutions and Services Companies.

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
• 1850+ global customers and growing.
• 2200+ in-house Regulatory experts.
• 12+ years of a strong foothold in the Regulatory industry.
• Have a presence across 25 global locations.
• 850+ in-country Regulatory affiliates across 120+ countries.
• ISO 9001 and ISO 27001 certified.

26/05/2026

🌍 Launching a Cosmetic product globally?

What works in one market may not always translate to another. From ingredient restrictions and product claims to labeling and registration requirements, even minor compliance gaps can delay a launch.

So where do cosmetic brands usually go wrong? 🤔
In this video, our Subject Matter Expert, Roshini Bandari, breaks down the most common mistakes brands make when expanding globally and shares practical insights to avoid them.

A must-watch for brands planning global launches or navigating multiple markets🌐

🎥 Watch the full video and follow Freyr for more Cosmetic
Regulatory insights.
https://www.freyrsolutions.com/contact

25/05/2026

India’s $50Bn Medtech opportunity is exploding. But CDSCO regulations are the biggest bottleneck.

Most companies think that entering India’s MedTech market is easy. It’s not.
India is one of the fastest-growing MedTech markets today, driven by rising healthcare demand, diagnostics expansion, and digital health innovation.

But here’s what many don’t realize: MDR 2017 didn’t just introduce regulation. It completely changed how approvals work.
Today, success depends on:
Getting device classification right
Identifying correct predicates
Responding to CDSCO queries with precision
Building technically sound documentation

Miss one of these? You’re looking at delays, rework, and lost time-to-market.

In this video, our Regulatory Expert “” shares what actually works based on real experience supporting 60+ clients and 300+ registrations in India.
If India is on your roadmap, lets connect to discuss your strategies

12/05/2026

✨ Clean Beauty.

🔍 Ingredient Transparency.

🌱 Sustainable Packaging.

These are no longer just trends; they’re redefining the future of the Cosmetics industry💄

Consumers today don’t just buy beauty products that deliver results; they’re also prioritizing ingredient transparency, sustainability, clean formulations, and conscious packaging choices.

In this video, our Subject Matter Expert – Roshini Bandari, shares insights on how consumer expectations are reshaping the Cosmetics landscape and the key trends brands cannot afford to ignore. 🚀

🎥 Watch the video & follow Freyr for more Cosmetic Regulatory insights.

https://www.freyrsolutions.com/contact

04/05/2026

Before you place a single product on the EU market, there’s one regulation you cannot ignore - GPSR.

The General Product Safety Regulation (GPSR) is now the new benchmark for product safety in the EU.

Recall Readiness, Product Safety Assessments, and Mandatory Responsible Person are no longer optional in the EU, and every detail matters.

In this video, we uncover 3 things brands often overlook under GPSR.

🎥 Watch the video to understand what changes and how to stay ahead of the Regulatory curve with Freyr
https://www.freyrsolutions.com/chemicals/general-product-safety-regulation-gpsr

07/04/2026

Safety Data Sheets (SDS) are more than just documentation—they are the foundation of chemical safety, OSHA compliance, and EU CLP regulatory adherence ⚠️

With evolving requirements under OSHA’s Hazard Communication Standard (HCS) and the EU CLP Regulation (22nd ATP), organizations must stay ahead of:
· New hazard classifications
· Updated labeling requirements
· Expanded SDS compliance expectations

📌 Outdated or non-compliant SDS can lead to serious regulatory, safety, and business risks.
👉 Are your Safety Data Sheets aligned with the latest OSHA, GHS, and EU CLP requirements for 2026?
👉 Watch now and follow Freyr for more insights on SDS authoring, chemical regulations, and global compliance trends.
https://www.freyrsolutions.com/chemicals/chemical-safety-data-sheet-sds-authoring-compliance-services

Think your SDS is compliant? You might want to double-check.With OSHA HCS updates and EU CLP 22nd ATP coming into effect...
31/03/2026

Think your SDS is compliant? You might want to double-check.

With OSHA HCS updates and EU CLP 22nd ATP coming into effect, even small gaps in your Safety data sheets can turn into big compliance risks.

From hazard classification to labeling - everything is under scrutiny.
We’re breaking down what brands often miss when it comes to SDS compliance.

🎥 Video dropping soon. Stay tuned.

Before your product hits the global shelves, Is your label actually complaint?One outdated ingredient name, one claim wi...
31/03/2026

Before your product hits the global shelves, Is your label actually complaint?

One outdated ingredient name, one claim without proof, and one missing detail - that’s all it takes to slow down a launch.

From the EU to the US and ASEAN, labeling laws aren’t universal, and we’re breaking down what brands must get right.

🎥 Video dropping soon. Stay Tuned!

18/03/2026

Brazil is one of Latin America’s fastest‑growing supplement markets, but success depends on strict ANVISA compliance. From classification and ingredient authorization to dossier submission and post‑market vigilance, every step matters.

With Freyr’s expertise, your supplements can meet ANVISA’s requirements and secure smooth access to Brazil’s booming market.

https://hubs.la/Q047hnfV0

17/03/2026

Your Cosmetic product is ready to conquer global shelves…
But is your Label compliant with evolving regulatory standards?

🌍 From INCI-compliant ingredient names and mandatory declarations to multilingual warnings and claim substantiation - One small miss can delay launches.

In this video, we break down what brands often overlook and how to get it right before your product reaches the global shelves.

🎥 Watch the full video & follow Freyr for more regulatory insights.
https://hubs.la/Q0472VDl0

At Freyr, we believe progress is shaped by diverse perspectives and empowered voices. Today we celebrate the women who c...
08/03/2026

At Freyr, we believe progress is shaped by diverse perspectives and empowered voices. Today we celebrate the women who contribute their expertise, leadership, and passion to building a stronger future every day.

27/02/2026

Europe’s deforestation‑free law is reshaping cattle exports. 👉 The process: 2020 cut‑off, geolocation traceability, extended deadlines. 👉 The impact: compliance secures EU market access, premium buyers, and consumer trust.

Freyr helps exporters build EU‑ready supply chains with due diligence systems, risk checks, reporting, and training.

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