About Us

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Company Profile

Ki3 Private Limited encompasses the essence of Knowledge combined with Innovation and Involvement with the notion of instilling sustained growth and steady progress in the clinical trial industry. A combination of enthusiastic and eminent teams from the clinical trial industry, Ki3 is managed by an accomplished team with more than 18+ years of industrial experience. The team, has handled several audits and inspections from pharma giants and international regulatory authorities. The team’s profound experience has provided them with an insightful understanding of the requirement for well-trained young professionals to tackle the challenging demands of the industry. Ki3 is a comprehensive clinical research organisation. We specialise in doing pre-clinical and clinical studies to assess the toxicity, safety and efficacy of Herbal, Ayurveda, Nutraceuticals, Cosmetics, Medical devices and other finished formulations.

Accreditations

Vision

Our Quality Policy embodies our commitment to achieving this vision by ensuring unwavering quality, regulatory compliance, continuous improvement, expanded expertise, international presence, and relentless innovation. At Ki3, we don't just aim to be leaders; we strive to make a lasting impact on the healthcare landscape.

Mission

Our mission is to provide efficient and high-quality clinical research services to support the development of safe and effective medical interventions and ensure adherence to ethical standards, regulatory compliance, and timely delivery of accurate and reliable clinical trial data.

Our Experience

Preclinical studies on small animal model’s Safety and Toxicity
Clinical Phase Studies
(Phase I to IV)
Comparative Clinical Trials to determine the safety and efficacy of Nutraceuticals
Exploratory Consumer
Research Studies
Patent filings/ applications done for Pharma companies
Scientific
Publications

Strengths and Advantages

  • End-to-end solution for AYUSH, Nutraceuticals, Cosmetics, Medical devices, and Allopathic requirements
  • Exclusive IEC for AYUSH and Drugs as per the recommendations
  • Combining strong technical capabilities with rapid turnaround time
  • Effective communication in terms of the proposal or query response
  • Studies adhering to the current regulatory requirements (IEC and CTRI)
  • Cost-effective solution without compromising on Quality

Quality Assurance

All our studies go through a systematic monitoring process to address the gaps, and necessary CAPA will be implemented to ensure the study goes through stringent QA criteria. All procedures follow a standardised SOP to verify alignment towards GCP and required regulatory standards. Our clinical research organisation is committed to meticulous quality assurance protocols. From precise data collection to comprehensive regulatory compliance, we guarantee exceptional standards throughout every research phase. Your trust in our quality assurance incites our commitment to advancing healthcare safely and effectively.