Regulatory Services in China
Freyr provides End-to-End Regulatory Services in China to pharmaceuticals, Medical Device, Food Supplements, Cosmetic and Consumer Companies to comply with NMPA Regulations. With Regional Delivery Centers, Client Servicing Centers and Offices in USA, UK, EU and India
Freyr Solutions ChinaChina cosmetic registration
Get expert guidance on China cosmetic import registration and filing. Ensure compliance with CSAR for both general and special use cosmetics. Freyr is a leading Regulatory solutions provider offering comprehensive services to life sciences firms across the regulatory spectrum.
Food supplements registration China
Get expert support for food supplements registration in China, ensuring full compliance with SAMR regulations and market entry with ease. Contact us today! China Food Supplement Regulation falls under the State Administration for Market Regulation (SAMR). The responsibility is shared between the state, provincial, municipal, and county-level authorities.
China Medical Device Registration
Freyr provides China medical device registration and approval support for device manufacturers that includes registration, classification, NMPA legal agent/representation services for product compliance as per NMPA & CMDE regulations. China is one of the fastest-growing markets for Medical Devices, where the demand for devices is majorly met through imports.
China Drug Registration and Approval
Freyr provides China Drug Registration and Approval support for pharmaceutical manufacturers that includes product classification, registration and approval for regulatory compliance as per NMPA regulations. As the world’s best pharmaceutical manufacturing powerhouse, China offers many business opportunities for pharma manufacturers
China NMPA Registration
Freyr provides End-to-End Regulatory Services in China to pharmaceuticals, Medical Device, Food Supplements, Cosmetic and Consumer Companies to comply with NMPA Regulations. Freyr is a leading Regulatory solutions provider offering comprehensive services to life sciences firms across the regulatory spectrum..
Agile Regulatory Strategies for a Dynamic Pharmaceutical Landscape
In today’s rapidly evolving pharmaceutical industry, companies face unprecedented challenges in navigating complex regulatory landscapes while striving to bring innovative therapies to market. The convergence of technological advancements, changing patient needs, and evolving regulatory frameworks has created a dynamic environment that demands agility and adaptability. This blog explores how pharmaceutical companies can implement agile regulatory…
Why is Regulatory Intelligence the Key to Local PV Success?
With global health authorities continuously updating their regulations, staying ahead of these changes is vital for life sciences companies. Local PV compliance, in particular, presents a unique challenge due to region-specific regulations, reporting timelines, and stringent requirements. This is where Regulatory Intelligence (RI) in PV becomes indispensable, helping companies stay informed and proactive. Navigating Local…
Product Registration and Listing as per USFDA Guidelines
In the highly regulated pharmaceutical and medical device industry, Product Registration and Listing with the U.S. Food and Drug Administration (USFDA) is a fundamental requirement for manufacturers and distributors looking to introduce their products into the U.S. market. Regulatory compliance is crucial to ensure patient safety, product efficacy, and market authorization. This blog explores the…
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