The Medical Device Single Audit Program, better known by its acronym MDSAP, is designed to increase audit efficiency by allowing a single audit to cover the requirements for Australian Therapeutic Goods Administration (TGA), Brazil’s Agência Nacional de Vigilância Sanitária (ANVISA), Health Canada, MHLW/PMDA, the U.S. Food and Drug Administration (FDA), and Japan Ordinance on Standards for Manufacturing Control. Although this… Read More
Prepare Your Organization for Medical Device Single Audit Program (MDSAP)
Is your business challenged by a complex and ever changing global regulatory environment? Medpoint can help! Preparing your business to be compliant to game changing requirements can be overwhelming. Medpoint has experts that can help you assess, plan, and implement strategies to effectively and efficiently stay ahead of emerging regulations and standards. Prepare your organization for Medical Device Single Audit… Read More