Your Trusted Partner for Comprehensive CRO Services, specialised in Medical Devices

At Qointa, we offer end-to-end support for life science companies, enabling them to focus on innovation while we handle the complexities of research, development, clinical trials, and regulatory approvals

Our Comprehensive Services

1. Clinical Trial Design and Management: We specialize in designing and managing clinical trials that adhere to the highest scientific and ethical standards. From protocol development to site selection, patient recruitment, and data collection, we ensure a smooth and efficient trial process.

2. Regulatory Affairs and Submissions: Navigating the complex regulatory landscape is critical for medical device companies. Our experts provide regulatory guidance and assist in preparing submissions, ensuring compliance with global regulations and standards.

3. Pre-Clinical Studies and Testing: Prior to clinical trials, rigorous pre-clinical studies and testing are essential. Qointa offers comprehensive pre-clinical services, including biocompatibility assessments, mechanical testing, and animal studies, to validate safety and efficacy.

4. Quality Assurance and Control: Quality is at the core of everything we do. Our quality assurance and control procedures are meticulously implemented to maintain the highest standards throughout the product development lifecycle.

5. Data Collection and Analysis: We employ advanced data collection and analysis techniques to derive meaningful insights from your trials. Our data experts ensure that you have the most relevant and accurate data at your disposal.

6. Post-Market Surveillance and Vigilance: Post-market surveillance is crucial for ongoing product safety and performance monitoring. Qointa provides vigilance services to identify and address any adverse events or issues promptly, ensuring patient safety and regulatory compliance.