MDC CONSULTANTS provides validation and regulatory products and services to the Pharmaceutical Industries. 

MDC devotes itself to the Pharmaceutical Industries. We offer validation and services directly to these industries and to equipment suppliers. Our services will assist you in complying to the most stringent, and latest regulations. We can supply your organization with Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification ( PQ) validation documents for virtually any process and utility equipment; we can even execute these documents at your discretion.  In summary, we create the validation documents required in regulated industries.

If your company supplies equipment to these industries, we can help make your products even more appealing. We help equipment suppliers during the design phase to assure the final product is compliant.  After the design phase we can create the required validation documents; a sought after feature by pharmaceutical and biotech companies.

We can commission As-built and As-found equipment, and create the required audit and validation documents. Do not delay; the best way to assure your product can be validated is to get us involved in the design phase! Is your product compliant with the electronic records regulations?

With our skills and experience, we can help your business tackle problems such as these:

• Quality System Development and Implementation

• Systems Regulatory Compliance

• Management of Projects from Design to Startup

• Information and Networking Technologies Business Solutions

• Computerized System Validation Policies and Guideline Development and Implementation

• Sterile and Non-Sterile Manufacturing and Packaging Systems Validation

• Quality Control/Research and Design Analytical Laboratory Systems Validation

Take a look at our MDC Brochure