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DADA Consultancy
DADA Consultancy
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Scientific Communications Development
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Defining the Value of Medical Affairs
Evidence Generation
Strategic Communications Planning
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Pharmacovigilance *
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Financial Services
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Facilities & Equipment
Testing & Release
Quality Management
Production & Supply Chain
Clinical Research *
Real World Data Research
Study Operations & Management
Clinical Reporting
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Automation & Efficiency
Data & Analytics
Early Development
Digital Health Solutions
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Informatics Infrastructure
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Projects
Medical Affairs *
Scientific Communications Development
Strategic Stakeholder Engagement
Defining the Value of Medical Affairs
Evidence Generation
Strategic Communications Planning
Regulatory *
Labeling & Promotions
Maintenance & Renewals
Compliance
Transparency & Disclosure
Commercialization *
Customer Engagement
Brand Planning & Activation
Market Access & Policy *
Government Policy
Global Market Access
Pharmacovigilance *
Safety Systems
Risk Management
Finance & Investment *
Financial Services
Investment Banking
Quality & Mfg *
Facilities & Equipment
Testing & Release
Quality Management
Production & Supply Chain
Clinical Research *
Real World Data Research
Study Operations & Management
Clinical Reporting
Product Development
Trial Design & Planning
Technology & Operations *
Automation & Efficiency
Data & Analytics
Early Development
Digital Health Solutions
Operations
Informatics Infrastructure
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About
![GxP Auditing](https://cdn.filestackcontent.com/A8cLeP4KaRV6aehNHMTkRz/resize=width:1000,height:1000/"https://cdn.filestackcontent.com/pkJfXDtkQxK7UDnAt0oX")
Overview
Using our vast network of experts, DADA can, either directly or via our sister-company ADOH, assist in the auditing efforts required to ensure a proper supply chain. We can audit active pharmaceutical ingredient manufacturers, finished dosage form manufacturers, analytical laboratories and wholesale dealers on your behalf, and perform a pre-inspection of your production facilities in order to prepare it for an inspection of EU healthcare authorities. Our experts can be available during the inspection (or customer audit) as well after the inspection/audit to help to correct any findings and non-conformities. We have substantial experience in supporting non-EU companies in preparation to their first EU GMP inspections. For more information on our GxP services, read the information on our website or contact us via email.
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