Case Study: Product and Business Registrations for Cosmetic Products in the UAE
In an era of expanding global markets, navigating regulatory landscapes in new territories poses significant challenges for companies aiming to […]
Case Study
Artixio Helps USA Pharma Company Register New Drugs on Time & on Budget Through Regulatory Staffing
Regulatory affairs (RA) is a critical function for pharmaceutical and medical device companies in the USA. RA professionals are responsible
A Case Study : Registration of Health Supplements in UAE
Navigating the complex regulatory landscape of a new market can be a daunting task for any company looking to expand
Case Study: Global Regulatory Intelligence for Dental Brand
Client: A global dental care brand headquartered in the United States. Problem Statement: The Client had portfolio of dental care
Artixio’s Regulatory Support for a Chinese Pharmaceutical Manufacturer in Mexico
A case study outlining Artixio’s Regulatory Support for a Chinese Client: Pharmaceutical Manufacturer in Mexico. Problem Statement A Chinese Pharmaceutical
Case Study: Enabling Product Positioning for Filtration Devices Using Primary Market Intelligence
Client Details: Client is a large scale, multi-industry conglomerate that markets filtration devices worldwide. Problem Statement: Client’s product leadership is
Case Study: Successful Registration of Software as Medical Device (SaMD) Assisting Surgical Procedure
Client: The client, a pioneering European company specializing in advanced medical technologies, sought regulatory approval for its innovative Holographic 3D
Case Study: Regulatory Contract Staffing for a US Based Biotech Company
Artixio provides expert regulatory staff on contingent and contract basis to pharmaceutical and other lifesciences industries using both its in-house
Case Study: Enabling Go/No-Go Decision for a Global Medical Devices Leader
Client: Client is a global medical devices leader with strong presence in syringes market. Problem Statement: The Company’s R&D department