Expert support in Pharma Consultancy, Regulatory Affairs, and GMP/GLP Training Programs for global compliance and growth.
Comprehensive pharmaceutical consulting solutions including GMP audits, turnkey project execution, regulatory dossier development, and seamless technology transfer services.
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Expert regulatory support including dossier compilation, DMF preparation, product registration, and end-to-end lifecycle management aligned with international regulatory bodies.
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Hands-on training sessions on GMP, GLP, regulatory compliance, and pharma quality systems delivered through expert-led workshops, simulations, and academic collaborations.
Read MoreFor over 15 years, Cyclone Pharmaceuticals Pvt. Ltd. (CPPL) has delivered top-tier pharmaceutical consulting services. Our founders bring over 25 years of in-depth experience to the industry.
CPPL excels in the development, implementation, and maintenance of pharmaceutical quality systems. Quality and GMP compliance are the pillars of successful pharma manufacturing.
Our Regulatory Division manages over 3000 files, with unmatched expertise in authoring and compiling dossiers, DMFs, and eCTD submissions for 90+ countries.
CPPL has trained countless professionals—from ground staff to management—in GMP fundamentals, offering both technical and compliance-based learning.
Audits Completed
Happy Clients
Dossiers / DMFs