CDAQi provide solutions to eliminate human errors to meet patient safety in hospitals and highly regulated compliance organizations.
CDAQI, the Global regulatory consultants in healthcare domains like Medical Device, Drugs & Pharmaceuticals. We are the company, founded and run by the Well-Qualified Regulatory Professionals.
We provide software validation, 21 CFR Part 11 evaluation, software quality systems audit services and trainings in IEC 62304 to FDA regulated companies.
We are the consultants serving organization to comply with 21 CFR Part 820, ISO 9001:2008 & ISO 13485:2003/EN ISO 13485:2012 requirements.
We are here to assistance you in Regulatory documentation, implementation, and Mock Audits.
We assist our clients to carry out the risk management process as per ISO 14971 requirements.
We help healthcare product manufacturers, traders, designers for acquiring country specific standards, to export healthcare products from one country to another as per regulatory requirements
CDAQi also provide total quality consulting solutions in association with Japanese Management and K S Madhavan & Associates, as our partners with proven industry practices to help our customers/clients produce quality products right at the first time.
With the support of SIJM & KSMA, CDAQI also help implement best practices of Western, Japanese & Indian Management Wisdom in organizations.
Together the three organizations provide residential trainings in Regulatory compliance and Modern Management techniques 5S, TQM, TPM, Poke Yoke, Lean Management) for SMEs.
Together the three organizations provide consulting services in Organization Transformation, turning around sick companies, Key Result Area and various process improvements.