Development, updating and revision of technical reports oriented to official registration, including compilation of scientific documents.
Preparation of technical documents to support registration, including experimental design and guidelines to conduct laboratory and clinical trials.
Follow-up of registration processes, from submission to compliance with complementary and legal requirements.
Assessment of product portfolio and strategy proposition to optimize results or for any possible acquisition/merger (Due Diligence).
Formatting technical reports and supporting documents for product internationalization.
Support in the development of proposals for new regulatory frameworks and in strategic assessments of the legislation in force.
These services can be provided jointly or separately, at the interested company's discretion, after preliminary assessment and a detailed analysis of the partnership proposed.
Should any services be extended to correlated areas, Vet Affairs has a network of partners to choose from.