GMP
Offers quality system improvement plant with Audits for Pharma Manufacturers
Regulatory
Dossier / DMF developement and Compilation and Registration services
Pharma Software
PaperLess GMP, QMS, Pharmacy and other Pharma Softwares
QA/ RA Forum
Interactive platform for Pharma technocrafts, quality professionals
About Us
India's Best Pharmaceutical GMP and Regulatory Consultant and worlds Leading Pharmaceutical Consultant with more than 22 years of Technical Experience.
Cyclone Pharmaceuticals Pvt Ltd is group company of Cyclone India Group. Established in 2005 as a small Pharmaceutical consultancy company by a Pharma technocrat Mr.Sachin Bhalekar. CPPL is growing as a Private Indian company with promoters quality approach and attitude.
Quality with cost effectiveness is the identity of Cyclone Pharmaceuticals Pvt Ltd.Time-line achievement is specialty of CPPL. CPPL Supports small Pharmaceutical companies to achieve a great milestone with registration of drug products,compliance of audits, preparation of Documents and it's implementation.
Cppl has associated Laboratories and CRO centers for Clinical, product development, analyticals laboratories in its service to perform consulting services with expertise. Consultant shall be with all knowledge and client shall get all what he/she is looking for in economy cost with highest quality is aim of Cyclone Pharmaceuticals Pvt Ltd.
Turn Key Projects
Turn Key project - Pharma Formulation and API plant setup consultancy services
Read moreeCTD & Regulatory Software
eCTD software for all region electronic compilation & submission of Dossier & DMF.
Read morePaperLess GMP Software
Paperless GMP Software - World's first PaperLess GMP software for Pharmaceutical Manufacturers.
Read moreVeripharma
Veripharma (Employee Verification Portal) - Pharma requirements and employee verfication portal.
Read morePharma B2B Portal
Pharma B2B Portal - B2B portal for pharmaceutical business developement.
Read moreDossier DMF Services
We have developed many products, ready dossiers & technologies to launch for manufacturing with 100% validation support at your manufacturing unit.
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Regulatory Affairs Technique
It provide strategic, tactical and operational direction and support for working within regulations to expedite the development.
3600 Documentation
It defines a system of information and control so that risks so inherent in misinterpretation and error in oral communication are minimized.
Audits and Regulatory Compilance
Assuring the good quality of product so that safe and effective product should be delivered to the public.
Standard Operating Procedure
To obtain the standard quality product intended for human use.
Technical Advisory for Business Growth
CPPL through its guidance is always assuring profit making solution for business growth
- Audit Compliance
- Dossier / DMF Support
- Cost Accounting Fundamentals
- Corporate Cash Management
- SEO Optimization Services
Pharmaceutical technical solutions at a glance
All kind of pharmaceutical business, technical and software services under one roof.