Microconsult, Inc. is a 17,000 sq ft. state-of-the-art scientific laboratory dedicated to helping manufacturers ensure product quality and integrity, as well as leading the industry in turnaround time for analysis.  We help businesses ensure compliance with federal regulations through validation of ingredients, helping them confidently deliver quality products to market. 

We are:

• FDA Registered
• DEA Licensed (Class 2, 3, 4 and 5 controlled substances)
• GMP/GLP Compliant
• ISO Certified
• ISO 17025

At Microconsult, Inc. we understand that whether your business is developing a new product or delivering established products to market, you have unique needs and technical requirements and require fast, reliable results.  To meet the needs of the most discerning manufacturers, we are staffed and equipped to be your preferred testing lab.

Our clients manufacture all types of products, including:

• OTC Drugs
• Cosmetics
• Sunscreens
• Raw Materials
• Medical Devices
• Vitamins
• Nutritional Products & Supplements

Our services include:

• Expert Analysis and Testing
• Method Development, Protocols and SOPs
• Analytical and Product Stability Tests
  • Shelf Life
  • Active Ingredient Assays
  • Preservative Efficacy Testing
  • pH, Viscosity, Color, Odor, etc.
  • Product Packaging Compatibility
  • Establishment of Expiry Dating
• Simple to Complex Chemical Analysis
• Microbiological Testing and Special Studies
• Nutritional Testing

We are dedicated to serving as an industry leader and distinguish ourselves from other testing labs with quality policies that we pride ourselves in and pledge to:

• Accurate and timely results and a commitment to continuously meet and/or exceed customer expectations through day-to-day interactions. 
• Unparalleled rapid turnaround time. 
• Every customer call is returned within 1-2 hours (during business hours) by personnel willing and able to answer questions, explain results and learn more about your specific needs.
• All Microbiology samples are tested the day they arrive.
• Utilization of USP, AOAC, ASTM and other methods (including our in-house validated analytical methods) where standard methods do not yet exist or are no longer valid in consideration of our updated state-of-the-art equipment. 
• Confidential, 24 hour access to results through on-line client portal.