The 07 in clinico department extends INVITROVO’s scientific pipeline from bench to bedside through tailored services, ensuring innovations progress into real-world healthcare settings. Our clinical division supports early human studies with tight adherence to ethical, regulatory, and scientific standards.
| Service ID | Service Title | Description |
|---|---|---|
| 07.01 | Ethical & Regulatory Approval | Full preparation and submission of ethics applications, working closely with Ethics Committees and Institutional Review Boards (IRBs) to secure Ethical Committee Approval. |
| 07.02 | Clinical Study Design & Protocol | Expert design of the study protocol, including the development of comprehensive regulatory documentation that aligns with national and international clinical research standards. |
| 07.03 | Early Phase Clinical Trials | Support for initiating and executing early human studies, specifically Proof of Concept Clinical Studies and Phase I Clinical Trials. |
| 07.04 | Therapeutic Area Focus | Specialized clinical support covering diverse therapeutic fields including Oncology, Gynecology, Ophthalmology, Dermatology, Orthopedics, and Endocrinology. |
| 07.05 | Patient Management & Logistics | Management of patient enrollment, ensuring proper informed consent procedures are followed, and coordinating on-site logistics for clinical activities. |
| 07.06 | On-Site Clinical Testing & Monitoring | Execution of on-site sample collection, clinical testing, vital sign monitoring, symptom tracking, and meticulous adverse event reporting by licensed clinicians. |
| 07.07 | Regulatory Compliance & Guidance | Continuous adherence to applicable Regulations and Guidelines, ensuring data integrity and full compliance throughout the trial lifecycle. |
| 07.08 | Clinical Outcome Analysis | Conducting longitudinal follow-up and performing rigorous analysis of clinical data to determine efficacy, safety, and validate clinical results. |
