Quality Systems
Robust quality management solutions aligned with GMP standards.
Pharmaceutical Validation & Quality Consulting
Validation & Qualification
End-to-end validation services across equipment, process and facilities.
Training & Support
Practical training and operational guidance for your teams.
Quality
Change Request Management
Deviation Management
CAPA Management
SOP Generation and Review
Quality Documentation System
Validation
Equipment Qualification
Process Validation
Cleaning Validation
Packaging Validation
Product Intermediate Hold Time
Temperature Mapping for Temperature Controlled Storage Areas
All Validation Related Document Generation (VMP, URS, FRS, TRS, FAT, SAT, IQ, OQ, PQ, PVP, PVR, CVP, CVR, PaVP, PaVR)
Training
Process, Cleaning, Packaging, Equipment Validation Studies, Evaluation and Document Generation (VMP, URS, FRS, TRS, FAT, SAT, IQ, OQ, PQ, PVP, PVR, CVP, CVR, PaVP, PaVR)
Temperature Mapping Studies, Evaluation and Document Generation (Protocol, Report and Risk Assessment)
About Us
Cycle Validation Services and Consultancy Limited provides validation, qualification and consultancy services with risk-based approach to the pharmaceutical, medical device and biotech industries.
The main purpose of Cycle Validation Services and Consultancy Ltd is to meet the validation and quality management requirements and training needs of pharmaceutical organizations in line with GMP standards. The other purpose is to perform these requirements in a cost effective and timely manner.
We have 18 years of extensive experience in quality, validation, production, and manufacturing & science technology areas in the pharmaceutical industry.