Exova offers regulatory consulting services in all aspects of product licensing.

Assisting clients in their development projects
Regulatory Consulting Services

With years of experience and industry knowledge, Exova’s regulatory consulting services can help you comply with global regulations and get your products to market faster.

Please Request a Quote online or contact us to find out how Exova’s Regulatory Consulting Services can assist you.

Regulatory consulting activities include:

• Regulatory consulting for National and European applications including administration and submission of expert summaries
• CTD Module 3
• Part II to Module 3 conversions
• Drug Master File plus quality overall summary
• Regulatory consulting for Mutual Recognition and Decentralized procedures
• Certificate of Suitability applications
• Veterinary Part II /expert reports
• Assessment/Registration of third party technical dossiers/technical due diligence
• Regulatory consulting in product license variations and renewals
• Technical Consulting Services

Exova’s regulatory consulting services ensure that your regulatory submissions are well prepared, and can avoid unnecessary delays in the review process. With our experienced project managers, we can assist you in navigating the regulatory mine field. Our regulatory consulting services can be provided on a short-term basis, or can become part of your own regulatory team as an additional resource providing the benefit of an independent opinion.