Goldman Regulatory Compliance106 Elizabeth St.
Providing Regulatory Affairs, Quality Operations and Business Development services to the Healthcare industry. Services include GMP Compliance (DEL, MDEL, Site License registration and renewal), regulatory dossier review (NDS, ANDS, DIN, MDL, NHP, VHP) prior to submission to Health Canada, conducting Pre-Inspection Audits (virtual and on-site), SOP writing and review, product label compliance and contract Quality Assurance.
- Innovative drugs
- Generic drugs
- Active Pharmaceutical Ingredients
- Veterinary medicine
- Medical devices
- Natural health products
- OTC/non-prescription drugs
- Drug/device combination products
- CBD Industry
- Business development due-diligence, market research and strategic planning. We are also able to act as your Canadian Representative VHP products manufactured outside of Canada.
- Europe (EU)
- Non-EU Europe
- Australia / New Zealand
- Latin America
ContactPhone: (Toll-Free) 844-265-1515