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Services

We are a highly focused GxP compliance and regulatory affairs service oriented company established in 2009. We’re a company that supports the toughest GxP compliance and regulatory affairs challenges.

We do more than consulting — we aim to make a remarkable impact on GxP compliance and Regulatory Affairs services. To achieve this mission, we’ve built a strong foundation. Our experts supported by young energetic team, has proven to be responsive and scalable through exponential growth since our inception in 2009.

Below is the focused service list.

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services
GCP
  • Project Management
  • Audits
  • Monitoring – Clinical
  • Monitoring – Bioanalytical
  • Monitoring – PK-Stat
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services
GMP
  • Audits
  • API Audit Reports
  • Compliance and Upgradation
  • Engineering
  • GMP Consulting
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Regulatory Affairs
  • Pre and Post submission services
  • Stand-alone
  • Intellectual Property Rights
  • Medical Writing
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Pharmacovigilance
  • Clinical Trial Pharmacovigilance
  • Post Authorization / Marketed Products
  • Global and EU PV Services
  • Medical Writing
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Concepts & Consulting
  • Plant Set-up and Due Diligence
  • CRO Setup
  • GxP Training
  • Software Support
  • Licensing