- Quality · Compliance · Excellence
Driving Quality.
Ensuring Compliance.
Accelerating Operational Excellence.
- Quality · Compliance · Excellence
Industries and Operations we transform with precision.
Manufacturing Facilities
Sector coverage
Packaging Operations
Sector coverage
Material Suppliers
Sector coverage
Warehouses
Sector coverage
Third-Party Laboratories
Sector coverage
Homecare Products
Sector coverage
Food & Dietary Supplements
Sector coverage
Cosmetics and Fragrances
Sector coverage
Pharmaceutical & OTC Drugs
Sector coverage
- Founder & Principal Consultant
CDR Global Enterprises
- About CDR Global
C.D.R. GLOBAL ENTERPRISES LLC
Committed, Driven, and Responsive
Vision
- Our Clients are business partners with us.
- Our Clients expect exceptional Customer - Supplier relationships.
- Our Clients expect and receive high-quality service at competitive pricing.
- Our Clients confidentiality is maintained.
- Our Clients seek us out for their improvement opportunities (new projects or continuous).
- Our Clients receive benchmark methodologies and state of the art training modules on improved systems/projects prior to start-up.
- Our Clients have overall improved product/material quality, their cost is driven down, and Quality Systems are more transparent, automated and digital based as a result of C.D.R. Global Enterprises
- Service Capabilities
Twelve disciplines. One unified standard of excellence.
Audits & Audit Readiness
Conduct full site and System audits of the facility and provide a detail report of all observations, including minor, major, or critical observations. Work with the facility on developing systemic plan to schedule, track, and measure the readiness for any internal or government inspection.
FDA & Regulatory Interfaces
Provide sitewide government inspection training to employees and plant audit host. Training includes a detailed process for interfacing/hosting and role responsibilities to ensure a successful Inspection.
Training Systems Development
Work with the facility on training and qualification of employees. Train the trainer programs and systems to track training within a manufacturing and warehouse environment.
Quality Assurance Systems
Work with the facility to design/set-up the appropriate QA System that fits your needs and will close and/or minimize any QA Risk/ Outage.
CQV Start-up Readiness
Work with the facility to establish the appropriate protocols for Standard Initiative Management and Product Launch requirements.
SPC & SQC Programs
Set up supplier qualification programs, on-line appropriate statistical sampling for incoming material inspections, including COA criteria and defect calibrations that will meet any government/customer requirements
GMP / cGMP Compliance
Work with the facility on appropriate GMPs for the specific business that meets quality and regulatory inspections.
Quality & Reliability Engineering
Work with the facility to develop operation of quality control systems, application and analysis of testing and inspection procedures.
Standards & Specifications
Work with the facility on the appropriate Standards/Specification management, review and tracking for good operational execution.
Problem Solving and CAPA
Apply statistical QC techniques in design and implementation of manufacturing processes to assure effective operations gaps are addressed, and the fixes are in place and sustained.
Lean Six Sigma
Six Sigma work is a customer focused quality initiative which provides an organizational vision of 3.4 defects per million opportunities. The "Six Sigma Quality" DMAIC cycle (Define, Measure, Analyze, Improve and Control) impacts bottom line results, proven to increase productivity, cut operating costs, enhance customer satisfaction, and reduce cycle time. "Six Sigma Quality" primarily focuses on the "Voice of the Customer" and secondly provides one common "Bar of Excellence" for employees to strive for near perfect products and services.
Fraud Examinations & Inspections
ACFE (Fraud Examiners) investigates the use of one's occupation for personal enrichment through the deliberate misuse or misapplication of the employing organization's resources or assets. The main reason behind the commitment of fraud is to achieve gain on false ground by illegal means.
- Why CDR Global
The benchmark difference, measured.
- Industry Expertise
- Regulatory Knowledge
- Customized Solutions
- Operational Excellence Focus
- Client-Centric Approach
- Long-Term Partnership Mentality
- Proven Quality Methodologies
- Continuous Improvement Culture
- Our Engagement Process
A disciplined path from, assessment to sustained excellence.
Discovery & Assessment
Deep operational diagnosis against quality, compliance and capability baselines.
Gap Analysis
Systematic mapping of risk, regulatory exposure and improvement opportunities.
Strategy Development
A prioritized roadmap aligned with your operations, regulators and growth objectives.
Implementation
Embedded execution support — SOPs, training, validation and rollout.
Monitoring & Optimization
SPC, KPIs and dashboards that prove sustained performance and audit readiness.
Continuous Improvement
Assembling a culture: Lean Six Sigma cycles, CAPA loops, capability growth.
- Results & Impact
Outcomes that prove the program works.
- FAQ
Questions, answered.
What industries does CDR Global serve?
Can you support FDA audit readiness?
How can CDR Global help your business specifically?
What does a typical engagement look like?
Do you offer long-term partnerships?
- Let's build excellence
Ready to strengthen your quality systems and compliance readiness?
crich@Globalenterprises.com
Phone
+1 (513) 348-3028
Headquarters
Roswell Georgia, 30047
Headquarters
20047 Windalier Way, Roswell Georgia, 30047