Freyr’s 510 (k) Compilation Receives the USFDA Approval For an Indian Wound Care Company


Posted May 28, 2018 by freyrsolutions

Freyr, a leading global Regulatory solutions and services provider, has successfully assisted a major medical device manufacturer in attaining the US Health Authority approval for their advanced wound care products.

 
New Jersey, May 29th , 2018 - Freyr, a leading global Regulatory solutions and services provider, has successfully assisted a major medical device manufacturer in attaining the US Health Authority approval for their advanced wound care products. Incidentally, the client has become the first Indian wound care product manufacturer to attain 510(k) clearance from the United States Food and Drug Administration (USFDA).

Freyr has meticulously strategized and compiled a 510(k) submission for the client, eventually procuring 510(k) clearances with the US FDA in expected timelines efficiently. Based on USFDA’s approval, the wound care product can now be marketed as Over the Counter (OTC) product in US.

“This is a significant milestone in Freyr’s growth journey as a specialized regulatory partner and the achievement has got our spirits further up to continue to ensure success for our global clientele. Our best regards for the client who have had their utmost trust in our capabilities,” said Suren Dheenadayalan, CEO at Freyr. “Freyr recently achieved another milestone of working with over 225 clients and this USFDA 510(k) clearance came just in time strengthening Freyr’s position as a preferred global regulatory partner. In line with our vision for future, we will continue to deliver such critical approvals from Health Authorities worldwide that has high business impact for our clients,” added Suren.

About Freyr

Freyr is a leading, niche, full-service global Regulatory Solutions and Services Company supporting, Large, Medium and Small Size Global Life sciences companies, (Pharmaceutical | Generics | Medical Device | Biotechnology | Biosimilar | Consumer Healthcare | Cosmetics) in their entire Regulatory value-chain; ranging from Regulatory Strategy, Intelligence, Dossiers, Submissions etc. to Post- Approval / Legacy Product Maintenance, Labeling, Artwork Change Management and other related functions.

Headquartered in New Jersey, USA, Freyr has regional offices across UK, Germany, UAE, Mexico, Singapore, Malaysia, South Africa and has Global Delivery Center in Hyderabad, India
225+ global clients and growing
550+ global Regulatory experts
700+ regional Regulatory affiliates across 120+ countries
ISO 9001 Certified for strong process and quality management
ISO 27001 Certified for information security management, state-of-the-art infrastructure
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Issued By Freyr Solutions
Country Virgin Islands (U.S.)
Categories Medical
Last Updated May 28, 2018