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Assessoria Regulatória

Regulatory Services

Specialized in records
of health products

Count on us for GAP analysis, dossier formatting in the CTD model and post-registration support, all in compliance with ANVISA's regulatory requirements.

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Assessoria Regulatória ANVISA

Is Your Company Ready to Meet ANVISA Requirements?

Submitting dossiers and maintaining the regulatory lifecycle require technical knowledge and compliance. Absence or failures in the process may result in rejections and delays in the commercialization of your product.

DC Regulatory works with:
​
  • Precise preparation of dossiers
  • Full compliance with ANVISA requirements
  • Reduction of regulatory risks
  • Complete regulatory lifecycle management

Strategic Solutions for Your Company's Regulatory Compliance

Our dedicated team provides comprehensive support for submission, registration and post-registration of medicines, health products and dietary supplements.
Produtos para Saúde
análise de gaps

GAP Analysis and Document Adjustments

(Identification and correction of faults)

dossiê

Preparation of Dossiers in CTD Format

(Registration of medicines and related products)

pós-registro

Full Post-Registration Support

(Price update, HMP, pharmacovigilance and more)

Why Choose
DC Regulatory ?

equipe especializada

Highly specialized team in Regulatory Affairs

atendimento ágil

Fast and personalized service for every need

suporte técnico

Full support for ANVISA compliance

tecnologia e inovação

Technology and innovation applied to regulatory management

Conformidade Regulatória

Ready to Strengthen Your Regulatory Compliance?

Minimize risks, avoid rework and have greater security when submitting your dossiers to ANVISA with the support of experts.
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