Compliance and Quality
RCM will work with you to set the direction, lay out the plan, and execute the plan, saving you time and money, as you optimize your Quality / Compliance programs by offering the following value-added services:
Compliance and Quality
Our Specialities
- Due Diligence Compliance Inspections, Audits & Assistance
- FDA Action (483 Observations, Warning Letters, Consent Decrees, Remediation)
- Mock FDA/International Regulatory Agency Inspections & PAI Readiness
- Post Audit Remediation
- Regulatory Compliance Assessments (FDA, EMEA, MHRA, DEA, ANVISA, COFEPRIS, Health Canada)
- Third-party GMP & GLP Compliance Auditing
- Policy, SOP & Batch Record Review, Preparation & Optimization
- QA Staff Augmentation
- Quality System (QS) Development, Assessment & Optimization
- Root Cause Investigations & Corrective & Preventive Action (CAPA) Planning & Execution
- Analytical Methods Validation
- Analytical Methods Transfer
- QC System Audit/Remediation
- QC Staffing
Contact Us
Have questions or want to speak with someone to find out how RCM Technologies can provide options for your business? Follow the link below and answer a few simple questions and a member of our solutions team will contact you to assess your requirements! Whatever your staffing or business requirements, we offer scalable solutions to fit your needs.