Since 2006, Regulatory Consulting has provided regulatory affairs and quality systems consulting services to the medical devices and in vitro diagnostics industries. Regulatory Consulting can assist you with a wide range of domestic and international regulatory affairs and quality systems requirements, including:
•FDA Establishment Registration and Listing
•US Agent for Foreign Manufacturers
•Premarket Notification 510(k)
•Investigational Device Exemptions (IDE)
•Premarket Approval Submissions (PMA)
•Technical File/Design Dossier for CE Marking (MDD and IVDD)
•Health Canada Licenses
•Foreign country regulatory submission
FDA and ISO Quality Systems Requirements
•Quality system audit
•Quality procedure review and gap assessments
•Labeling review and gap assessments
•Design control protocols and report
We will assist you in understanding domestic and international regulatory requirements and delivering your products to market in a timely fashion.
Visit the Services link to find out more about our capabilities and experience.
We also have direct experience networking with a number of experts in product-specific requirements, including product safety engineering to IEC standards, sterilization, biocompatibility, packaging validation, and FDA and IEC laser regulations.
Visit the Links page to access the services of our recommended colleagues.