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Guide the Pharma Industry

World’s Leading Pharmaceutical Consultancy Company
Experts Serving the Pharma Industry for Over Two Decades

Learn More About Our Pharma Consultancy Expertise

GMP Compliance

Audit Consultants

India’s Leading GMP Compliance Experts
Delivering Audits and Regulatory Support with Modern, Digitalized Solutions

Explore Our GMP Audit & Compliance Consulting Services

Technology Transfer

Registration Dossiers

End-to-End Pharma Technology Transfer Services
Validated Dossiers for Global Submissions

View Our Pharma Dossier Preparation & Tech Transfer Services

Project Designing

Turnkey Projects

Regulatory Layout Design & Implementation
Complete Execution of Turnkey Pharmaceutical Projects

Discover Our Turnkey Pharmaceutical Project Solutions

Pharma Regulatory

& Registration Consultants

CPPL Specializes in Regulatory Submissions, Dossiers, DMF Writing, and Compliance Training
Trusted Experts for Global Regulatory Support

Learn About Our Regulatory Affairs & Pharma Documentation Services

Industry-Leading

Pharma Training Programs

CPPL Empowers Professionals Through Specialized Training
Covering GMP, GLP, Biologics, and Medical Device Regulations

Explore Our Pharma Training & Certification Programs
Affordable and Tailored Pharmaceutical Solutions

CPPL Pharma Technical Hub

Expert support in Pharma Consultancy, Regulatory Affairs, and GMP/GLP Training Programs for global compliance and growth.

Pharma Consultancy

Pharma Consultancy Services

End-to-end pharmaceutical consulting solutions delivering GMP compliance audits, turnkey facility design, CTD/eCTD regulatory dossier development, and optimized technology transfer systems to accelerate approvals and achieve global regulatory readiness.

Explore Our Complete Services

Regulatory Affairs

Regulatory Affairs Services

Expert regulatory support providing dossier compilation, DMF preparation, product registration guidance, and complete lifecycle management aligned with global regulatory authorities to ensure seamless submissions and international compliance success.

Learn About Our Regulatory Affairs

Pharma Trainings

Pharma Training Programs

Hands-on training programs covering GMP, GLP, regulatory compliance, and pharmaceutical quality systems through expert-led workshops, real-world simulations, and specialized industry–academic collaborations to strengthen organizational competency.

View Pharmaceutical Training Programs

Who We Are?

Cyclone Pharma is renowned for providing knowledgeable services that are timely and committed.

  • Pharma Consultancy
  • GMP & Audits
  • Regulatory Services
  • Business Development
  • Technology Transfer
  • PaperLess GMP
  • Training Services
  • Pharma Dossiers
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Technical Expertise

Why Choose Us

For more than 15 years, Cyclone Pharmaceuticals Pvt. Ltd. (CPPL) has been a trusted leader in pharmaceutical consulting and regulatory compliance services. Backed by founders with over 25 years of industry expertise, we provide end-to-end solutions that support global pharmaceutical operations.

At CPPL, we specialize in the development, implementation, and maintenance of robust pharmaceutical quality systems. Our focus on Quality Assurance (QA) and Good Manufacturing Practices (GMP) compliance helps companies achieve consistent, audit-ready, and regulatory-approved manufacturing processes.

Our Regulatory Affairs Division manages 3,000+ regulatory files, offering exceptional proficiency in dossier preparation, Drug Master Files (DMFs), CTD/eCTD submissions, and global regulatory documentation for 90+ countries across regulated and semi-regulated markets.

CPPL has also trained thousands of pharma professionals—ranging from entry-level teams to senior management—in GMP training, pharma quality systems, and regulatory compliance. Our tailored technical and compliance-based programs help organizations strengthen operational excellence and meet international regulatory expectations.

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Audits Completed

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Happy Clients

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Dossiers / DMFs

GMP Projects
85%
Regulatory
90%
Training
75%
Turn Key Projects
70%
Technology Transfer
90%
Our Works

Latest Projects

Paperless GMP Project by CPPL
Paperless GMP Project

by CPPL

Quality Integration Program by Pharma QA
Quality Integration Programme

by Pharma QA

GMP Training Session by CPPL
GMP Training Sessions

by CPPL

eCTD Software Implementation
eCTD Software Implementation

by CPPL

Quality Excellence & Research Center
Quality Excellence & Research Center

by CPPL

QMS Upgradation by CPPL
QMS Upgradation

by CPPL

Turn Key Project by CPPL
Turn Key Project Execution

by CPPL

Pharma Audit Project by CPPL
Pharma Audit Program

by CPPL

Quality Services with Cost and Commitment

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