Schedule Consultation
  • Home
  • FAQs

FAQs

  • FAQ

Questions, answered.

With our 25+ years of experienced consultants, we support several industries, Medical Devices, Foods, Cosmetics & Fragrances, Dietary Supplements, Pharmaceutical, Over the counter (Drugs, and Beauty products for both manufacturing operations and material supply (Raws/Pack Materials).

CDR Global provides FDA readiness training to the facility on best process for hosting an FDA Inspection, the appropriate structure that would assure that the inspector receives the requested information in a timely manner, and what documents can be shared and the ones the organization is not required to share with the inspector. The facility would receive a ” Guide to FDA Inspections” document that could be used in prep for any future inspection.

The CDR Global consultants dive deep into your process, find hidden opportunities for growth, efficiencies and risk. We then work with your facility to develop the appropriate quality/operational system to improve and sustain the improved process.
Once CDR Global receives your request for a consultation, we will set up a meeting for a short discussion to understand your needs, your objectives, and what you see as success. Timing for completion, depends on your goals, the current gaps (current state), but we always prioritizes quality, efficiency and results. We will scope out the work and provide a detailed SOW for review and feedback. CDR Global goal is to assure your objectives are being met, and a high-quality job is being done.
Yes, CDR Global has a goal to establish a long-term relationship with its clients. We believe a strong customer-supplier relationship with common objective is a key component for ongoing sustain improvements. We support ongoing training needs, coaching, and contract services.