Northumbria Pharma also has a dedicated regulatory team comprising Qualified Persons (QPs) and regulatory assurance specialists who are adept at navigating regulatory changes to ensure access to innovative medicines. Our comprehensive services include: 

• Preparation of regulatory dossiers for Marketing Authorisation Applications
• Conducting service or product supplier audits
• Reviewing Technical agreements to ensure compliance
• Providing QP services on a contract basis

Our team’s skill in navigating regulatory requirements and resolving issues guarantees that our regulatory submissions are expedited smoothly, facilitating timely delivery of our innovative products to the market.