DiaSYS provide its services to pharmaceutical, Biotechnology, Medical Device to achieve optimal time to market for their product and to maintain compliance in their operation, as we believe a regulatory strategy is the key to success in drug and device development. Our highly qualified staffs uses an integrated project management approach to work with our clients.
Our Regulatory Affair Services Covers:
- Providing support to resolve regulatory citations
- Regulatory submission and registration of product
- Regulatory audits preparations
- cGMP Training