Riya Interactive Inc.
Consulting firm providing quality, compliance, validation, design controls, and IT services for medical device, diagnostics, and pharmaceutical programs. Offers end-to-end support from R&D through manufacturing and regulatory submissions, with emphasis on audit-ready documentation, paperless validation, and regulatory readiness for global markets.
Industries
N/A
Nr. of Employees
small (1-50)
Riya Interactive Inc.
Services
QMS development, remediation, audit readiness, and inspection support to align with regulatory requirements.
Development and execution of IQ/OQ/PQ, process validation, media fills, and computer system validation to ensure compliant manufacturing and testing.
DHF remediation, ISO 14971-based risk assessments, FMEA, and human factors engineering to support device development and regulatory requirements.
Preparation of regulatory dossiers and technical files for FDA and international submissions and compliance documentation (e.g., 510(k), PMA, BLA, ANDA, NDA).
Blueprinting labs, selecting analytical equipment, performing method validation, and configuring LIMS/ELN systems for traceability and compliance.
Implementation and integration of EDMS, eQMS, enterprise systems, analytics, and compliance-ready workflows.
QMS development, remediation, audit readiness, and inspection support to align with regulatory requirements.
Development and execution of IQ/OQ/PQ, process validation, media fills, and computer system validation to ensure compliant manufacturing and testing.
DHF remediation, ISO 14971-based risk assessments, FMEA, and human factors engineering to support device development and regulatory requirements.
Preparation of regulatory dossiers and technical files for FDA and international submissions and compliance documentation (e.g., 510(k), PMA, BLA, ANDA, NDA).
Blueprinting labs, selecting analytical equipment, performing method validation, and configuring LIMS/ELN systems for traceability and compliance.
Implementation and integration of EDMS, eQMS, enterprise systems, analytics, and compliance-ready workflows.
Expertise Areas
- Quality management systems (QMS) development and remediation
- Regulatory submissions and compliance (FDA, EU, ICH)
- Validation and qualification (IQ/OQ/PQ, process validation, CSV)
- Design controls, risk management, and human factors
Key Technologies
- LIMS and electronic lab notebook systems
- Electronic document management systems (EDMS) and eQMS
- Paperless validation platforms
- Computer system validation (CSV) and GAMP 5 practices
News & Updates
Women's Business Enterprise certification.
Minority Business Enterprise certification.
Small Business Administration Women-Owned Small Business certification.
Women's Business Enterprise certification.
Minority Business Enterprise certification.
Small Business Administration Women-Owned Small Business certification.