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Regpro

Regulatory Document Solutions for Pharma Industry

  • Clyzo’s trademark regulatory program
  • Fast Manufacturer and Product qualification
  • Quick help with regulatory queries
  • Backed by expert compliance team
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What We Offer

We provide regulatory documentation, risk assessment, manufacturer qualification, audit readiness and compliance expertise.

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Elemental Impurities (ICHQ3D)

Ensure compliance with global impurity standards.

Nitrosamine Risk Assessment (IPEC)

Comprehensive risk evaluation for nitrosamines.

Manufacturer Qualification

Validate and qualify suppliers and manufacturers.

(ISO/cGMP/IPEC) Certificate

Access industry-standard certifications.

TSE-BSE / Allergen / Melamine

Confirming all pharma declarations.

Residual Solvent Certificate

Meet stringent solvent residue criteria.

DEG & EG Certificate

Compliance documentation for diethylene glycol and ethylene glycol.

Site Audit & Technical Agreement

Robust site assessments and agreements.

Why Choose RegPro?

Accelerate your regulatory journey with expert support & faster qualifications.

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Centralized Compliance Solution

All your regulatory documents in one place.

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Global Standards

Compliance with USP-NF, BP, EP, JP, and cGMP guidelines.

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User-Friendly CTD Format

Ready-to-use Common Technical Dossiers (CTD's) for quick excipient compliance.

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Expert Support

Dedicated technical team for seamless assistance.

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Looking for Customized Regulatory Solutions: Your Search Ends Here!

Talk to Our Technical Team

Guidance You Can Trust: Expert Assistance for Your Regulatory and Compliance Needs

regulatory@clyzo.com

+91 8655 687 716

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