DADA Consultancy

Exhibitor

DADA Consultancy is a specialized, independent European consultancy firm with over 40 years of experience, providing comprehensive regulatory, pharmacovigilance, quality assurance, and market access services for human and veterinary medicines and nutraceuticals; acting as a "virtual department" for many clients or supporting internal client teams with expert advice for EU market entry and compliance. We focus on tailor-made solutions, project management, compliance, feasibility studies, while maintaining high quality standards (ISO 9001 certified) and fostering long-term partnerships with our clients. 

Our Key Services offered include:

• Regulatory Affairs: Managing EU regulatory procedures (CP, DCP, MRP), variations, and acting as a virtual RA department.
• Pharmacovigilance: Setting up systems, PV audits, QPPV (network) support, acting as a virtual PV department.
• Product Development: Feasibility studies, project management, clinical support, and GMP documentation for marketing authorization.
• Quality Assurance: GMP/GLP/GDP auditing and compliance, support with the set-up of a QMS for MIA/WDA licenses.
• Market Access & Advertising: Compliance with local advertising rules and reimbursement strategies.
• MAH ownership and QP Batch Release: through our sister company ADOH, we can offer MAH ownership to support your regulatory strategy, and we have QP's on board for EU Batch Release

DADA excels in Project Management where we can handle complex drug development and registration projects and we can also have our consultants to address any Organizational Support questions to provide advice on setting up internal regulatory, PV or quality departments. 

Our Core Strengths:

• Deep expertise in EU regulations.
• Long-term partnerships and high client satisfaction.
• ISO 9001 certified for quality.
• Extensive network of experts and partners

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