Rare Moon | Orphan Drug Regulatory Affairs
Biotechnology, 8 Market Pl, Baltimore, Maryland, 21202, United States, 1-10 Employees
Phone Number: +14*********
Who is RAREMOON | ORPHAN DRUG REGULATORY AFFAIRS
We work exclusively on orphan drugs and advanced therapies. We advise, develop, write, review, and submit regulatory dossiers. Our regulatory team brings over 100 combined years of indust...
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- Headquarters: 8 Market Pl, Baltimore, Maryland, 21202, United States
- Date Founded: 2016
- Employees: 1-10
- Revenue: $1 Million to $5 Million
- Active Tech Stack: See technologies
- CEO: Sabrina Mogle
Industry: Biotechnology
SIC Code: 8731
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Frequently Asked Questions Regarding RareMoon | Orphan Drug Regulatory Affairs
Answer: RareMoon | Orphan Drug Regulatory Affairs's headquarters are located at 8 Market Pl, Baltimore, Maryland, 21202, United States
Answer: RareMoon | Orphan Drug Regulatory Affairs's phone number is +14*********
Answer: RareMoon | Orphan Drug Regulatory Affairs's official website is https://raremoonconsulting.com
Answer: RareMoon | Orphan Drug Regulatory Affairs's revenue is $1 Million to $5 Million
Answer: RareMoon | Orphan Drug Regulatory Affairs's SIC: 8731
Answer: RareMoon | Orphan Drug Regulatory Affairs has 1-10 employees
Answer: RareMoon | Orphan Drug Regulatory Affairs is in Biotechnology
Answer: RareMoon | Orphan Drug Regulatory Affairs contact info: Phone number: +14********* Website: https://raremoonconsulting.com
Answer: We work exclusively on orphan drugs and advanced therapies. We advise, develop, write, review, and submit regulatory dossiers. Our regulatory team brings over 100 combined years of industry and consulting experience in orphan drug regulations and development. Made up entirely of Ph.D./MS-level/MD, senior regulatory strategists and mechanics, and all the passion in the world, they lead programs to success. Our Clients are those looking for strategic and operational support; someone who can be eyes-on and hands-on their program as and when needed; someone to help them navigate this complex regulatory pathway, and help them to decide when and how to submit their orphan applications, applications for accelerated approvals, and interactions with the Agencies. They hire us to incorporate data from the smallest of populations coupled with novel therapies into the purest blend of science, regulations, patient care, and corporate objectives. We help them to maneuver the product through the regulatory framework, steering the data into a regulatory position that is poised to accelerate into marketing as early as possible. They trust our team, as we continue to work fast and hard to ensure their success. We plan, formulate questions, write, review, and/or submit. - Regulatory operations - Strategy & Development - Medical Writing - Publishing Visit our website to hear what our clients are saying about us.
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