Research Triangle Park Laboratories, Inc.

"Scientists with Solutions - Since 1970"

    7201 ACC Blvd., Suite 104, Raleigh, NC   27617     New address June, 2008 

    Telephone: (919) 510-0228; Fax: (919) 510-0141       

    E-Mail: CustomerService@RTP-Labs.com                                                                                                           ISO 17025 Compliant

 Analytical Laboratory Testing Services

  • US and Foreign Imported Products Testing for Contamination, Toxic Chemicals, Pesticides, VOCs; Banned Substances; Product Purity.

  • Indoor Air, Ambient & Sources (Stack Gases), VOC Vapor Intrusion, Dissolved Gases in Groundwater, Landfill Gases, Soil & Water, Pesticides, Perfluorooctanonic Acid (PFOA) & Fluorinated Telomers, Phthalates, PCBs, Isocyanates, Semivolatile Organics, Siloxanes, EPA, NIOSH, OSHA, ASTM Test Methods.

  • Pharmaceuticals; Residual Solvents; Controlled Substances.

  • Dietary Supplements Testing to support the new June 2007 FDA Current Good Manufacturing Practice (cGMP) Rule;  Effective Date Aug. 24, 2007.

  • Sustainable products, "Green Building" and LEED chemical emissions testing using ASTM D5116 "Environmental Chambers" and the California's Section 01350 "School Building Specifications" methods.  Testing of air cleaners for emission of ozone by UL-867 (ver. 2007), CADR, odors and particle removal efficiencies.

  • Custom Projects and Research & Development.

RTP Labs is compliant with ISO 17025 Standard for laboratories, is a State of Pennsylvania Registered Laboratory and Federal Drug Enforcement Agency & North Carolina Controlled Substances Registered Analytical Laboratory.

Contract Analytical Laboratory Services for Environmental, Pharmaceutical, Biotechnology, Dietary Supplements, and Manufacturing Industries

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Analytical Laboratory Services

 

for

 

Dietary Supplements

Services Offered
  •  Active Component or Ingredient Testing
  •  Residual Solvents & Impurity Identifications
  •  Analytical Methods Development & Validations
  •  Stability Studies; Research & Consulting Projects
  •  Certificate of Analysis Confirmation of Ingredients

Instrumental Methods

  •  HPLC/PDA and Fluorescence Detectors
  •  Gas Chromatography/Mass Spectrometry
  •  GC/FID; /FPD; /TCD; /HALL; /ECD; /PID
  •  UV Spectrophotometer & Headspace Analyzers

Quality Assurance

  •  June 25, 2007 new FDA rule 21 CFR Part 111 requires Current Good Manufacturing Practice (cGMP) in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements.  100% identity testing is required unless exempted by FDA.
  •  The FDA Rule requires the establishment of specifications in the production and process control system that will ensure dietary supplements meet the identity, purity, strength, and composition established in specifications and are properly packaged and labeled.
  •  Test methods must be scientifically valid.
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