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Guide Pharma Industry

Worlds Leading Pharmaceutical Consultancy Company
Pharma Experts serving Pharma Industry for two decades.

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GMP Compliance

Audit Consultants

India's best GMP Consultant,Consulting for GMP Audits and Compliance
GMP With advanced concept and digitalisation.

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Technology Transfer

Registration Dossiers

Pharma Research and Transfer of Technology
Dossiers with Validated Technology

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Project Designing

Turn Key Project

Hands on Experience in Regulatory Layout Designing
Execution of Turn Key Project

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Pharma Regulatory

and Registration Consultants

CPPL works for Regulatory Compliance ,Dossier,DMF Writing,Regulatory Training
We are experts of Dossier and DMF .

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Best Pharma

Training Center

CPPL Make the experts by improving knowledge of Pharma Professionals with its World class training Programmes
GMP/GLP/Biological/Medical Devices Training .

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Affordable and Perfect Solutions

CPPL Pharma Technical Hub

Pharma Consultancy

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Best-known for its end-to-end pharmaceutical consulting services, GMP audits, turn-key projects, regulatory dossiers, and technology transfer.

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Regulatory Affairs

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Perfect Pharma Regulatory Services. Review Services, Dossier Technology Transfer, Dossier DMF Compilation and Registration.

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Pharma Trainings

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Tech workshops and sophisticated concepts for Pharma Training Services Pharma Technocrates receive hands-on training services.

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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 the past 15 years, Cyclone Pharmaceuticals Pvt Limited has provided high-quality pharmaceutical services to the pharmaceutical industry. The organization's promoters have over 25 years of experience in the field.

Cyclone Pharma has experience and skill in developing, implementing, and overseeing quality systems. Quality systems and GMP are the foundation of pharmaceutical manufacturing.

The CPPL Regulatory Division handles over 3000 files and possesses the necessary competence in writing and compiling dossiers, DMFs, and eCTD submissions for over 90 countries.

As of right now, GMP and Pharma training has taught a lot of employees, workers, and students alike.CPPL also teaches management the fundamentals of the pharmaceutical industry's GMP structure.

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Audits Done

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Satisfied Clients

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Dossiers/DMF

GMP Projects
50%
Regulatory
25%
Training
15%
Turn Key Projects
5%
Technology Transfer
10%
Our Works

Latest Projects

Quality Services with Cost and Commitment

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