Freyr Successfully Submits NCE-1(ANDA) to USFDA For Crystal Pharmaceutical
By: Freyr Solutions
For such an NCE-1 (ANDA) project, pharmaceutical companies across the globe competed for the 180 days marketing exclusivity for their generic version of the product used for the treatment of chronic heart failure. To secure this goal, the NCE-1 (ANDA) has to be filed to the USFDA on time, in addition to passing bioequivalent test to reference listed product.
Freyr, with a clear-cut perspective on the exclusivity, took over the challenge and went for comprehensive gap analysis, meticulous dossier compilation, review, and publishing of 35,000 pages of the NCE-1 (ANDA). By proactive planning and collaboration with our client, Freyr ensured timely and successful submission with RTR-free. Five different in-house Regulatory teams of Freyr worked together for this submission.
"As a global Regulatory services provider, aligning to clients' unique requirements is our top priority. And this critical yet successful NCE-1 (ANDA) submission is just another testimony for it," said Suren Dheenadayalan, CEO, Freyr. "Though the project was demanding timely allocation of resources for meticulous review, and timely publishing and submission, we as a team feel accomplished in winning the clients' confidence not only in successful submission of NCE-1 (ANDA), but by making it with no RTRs. Having this opportunity boosts our confidence and elevates our industry leader position to a newer height," added Suren.
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 | Chemicals) in their entire Regulatory value-chain;
Headquartered in New Jersey, USA, Freyr has regional offices across UK, Germany, UAE, Canada, Mexico, Singapore, Malaysia, South Africa, Slovenia, Austria, Sri Lanka and has Global Delivery Center in Hyderabad, India.
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