State (California...)
FDA, ISO Regulatory Affairs in California
FDA and ISO Regulatory Affairs Consultants in California: FDA and ISO medical device consultants serving Southern/Northern California.
Relevant State Agencies
California State Agencies (Sacramento, CA)
Services
Medical Business Startup
- Business Plan, Funding (Seed Capital)
- R&D, Prototypes, Design Validation and Design Controls
- Manufacturing
- Strategic Planning, Marketing and Distribution
FDA 510K Notifications
- Traditional 510(k)
- Special 510 (k)
- Abbreviated 510(k)
State Regulations
- State Regulatory Guidelines and Requirements (CA, WA, OR, AZ, NY, NJ, FL…)
- Local government regulations in Northern California (San Jose and San Francisco) and Southern California (San Diego, Orange County and Los Angeles-LA)
NDA New Drug Applications
PMA Pre-market Approvals (Class III)
Quality Systems
- ISO Quality Systems Implementation, Certification and Registration Consulting
- ISO 13485, ISO 9001, ISO 13488:2000
- CE Marking and EU Medical Device Directives Compliance (MDD, IVDD, AIMDD)
- Audit preparation, documentation, training...
Supplements and Alternative Medicine
- Applied Nutrition
- Botanical Drugs
- Dietary Supplements
- Importing from Asia
Laboratory Compliance Testing
- FDA, UL and CSA
- CE and EU MDD
- IEC 60601-1 and 61000-1 (EMC), ETL, EMI
- Biocompatibility and Toxicity
- Clinical Trials
Risk Management
- Risk Assessment, Hazards Analysis, FMEA, FTA, HFE…
- FDA Guidelines
- ISO 14971
International Regulations
- Import/Export Permits
- Europe/Asia Product FDA approvals for US Market
- FDA Authorized Representative and US Agent
- Global Distribution (Canada, Germany, UK, France, China, Japan, India...)
- US Medical Products Asian and EU Approvals