FDA ComplianceFDA ComplianceFDA Compliance
FDA Compliance - HomeFDA Compliance - AboutFDA Compliance - CapabilitiesFDA Compliance - ServicesFDA Compliance - NewsFDA Compliance - ContactFDA Compliance - Sitemap

CGMP Pro Capabilities

At CGMP Pro our pharmaceutical consultants are able to provide expert assistance in helping you to achieve CGMP compliance in a variety of product manufacturing and support operations. These include:

Manufacturing Operations
  • Finished products
    • Solid oral dosage forms (tablets, caplets, capsules, liquid-filled gelatin, sachets)
    • Liquid orals
    • Sterile injectibles (SVP, LVP)
    • Lyophilized products for reconstitution
    • Trans-dermal delivery
  • Active Pharmaceutical Ingredients (APIs: liquids and solids)
  • Pilot plants, clinical supplies manufacturing
  • Excipient manufacturing
  • Packaging and labeling
  • Repackaging
Manufacturing Support Operations
  • Chemistry Laboratories
  • Microbiology Laboratories
  • Warehousing and distribution
  • Water systems, HVAC, Electrical Power distribution
Facility Design Review
  • New Construction
  • Refurbish Existing Facility

FDA Compliance