Suppliers Audit
Providing full-life cycle solutions for MAH project
Suppliers Audit

Canny support for the third-party audit covering drug substance, excipients, packaging materials, and consumables according to ICH, ISO, PIC/S guidelines, we will also pay attention to the possible gaps for each suppliers with reference to the Provincial MPA’s specific reequipments that the Holder located and future development plan.

Your Trustworthy Consultant for Drug Regulatory Compliance

With 25 years of continuous dedicated services for pharmaceutical industry, Canny has provided professional services for 2000+ projects, including 20+ one-stop services for MAH project customers to help them to plan for the whole project, to set up MAH systems, to train to upgrade key personnels, to audit CDMO & key materials suppliers, to guide for License B application and inspection acceptance, among which two of projects passed the Provincial MPA’s inspection with “0” deficiencies!

CANNY-Your Trustworthy Consultant for Drug Regulatory Compliance!
  • 25 years
    of professional consulting experience in the pharmaceutical industry
  • 700 +
    GMP certification projects for China, EU, FDA, UK, Japan, Australia and WHO inspection
  • 320 +
    Validation execution and guidance projects
  • 2400 +
    Globally RA registration projects
  • 1370 +
    Globally clients and pharmaceutical partners
  • 30 +
    Experts from China, US and EU
Professional Services, Standardized SOPs

Providing full-life cycle solutions for MAH project

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