Regulatory Submission Management Services
CDN’s Regulatory Submission Service is the latest addition to the comprehensive list of services we provide. Many regulatory affairs departments now rely on our team of highly dedicated professionals.
We prepare and complete applications for submission to the MHRA, EMA, DoH, BIS and Defra on their behalf relating to drugs, medicines, pharmaceuticals, chemicals and medical devices for both human and veterinary products.
Working directly with our clients as an extension
of their teams, we provide a complete Regulatory Submission Service.
CDN can provide a truly one step solution to your regulatory affairs department requirements in a fast, efficient and cost effective manner. Our experienced team is always on hand to provide friendly service and professional advice.
Our Regulatory Submission Services team can prepare, complete and submit your applications for you. Typical applications include:
- • MHRA - CPP and GMP
Certificate Applications - • EMA - CPP Certificate Applications
- • DoH - Free Sale Certificate Applications
- • BIS - Free Sale Certificate Applications
- • Defra - Free Sale Certificate Applications
- • VMD - Free Sale Certificate Applications