Aarogyaline’s Specimen Management and Collection Services encompass
Managing project coordination and logistics
- Creating collection protocols and Case Report Forms (CRFs)
- Designing HIPAA-compliant patient Informed Consent Forms (ICFs)
- Handling Institutional Review Board (IRB) submissions
- Setting up, training, and monitoring collection sites
- Providing necessary supplies and equipment
- Overseeing project management and logistics coordination
- Monitoring clinical data and ensuring completion of reports
- Resolving any queries that arise
- Supporting longitudinal studies by collecting specimens from diagnosis through treatment cycles and remission phases.
Tissue Microarray & Histology
- Aarogyaline facilitates selection and procurement of tissue samples from diverse sources, including biobanks, clinical repositories, and research institutions.
- TMA Construction: Aarogyaline constructs tissue microarrays by arraying small tissue cores from individual samples onto a recipient block, ensuring uniformity and consistency.
- Histological Analysis: Aarogyaline conducts histological analysis to verify tissue sample quality and integrity before TMA construction.
- Custom TMA Design: Aarogyaline collaborates with clients to design custom TMA layouts tailored to their research needs, selecting appropriate tissue types, disease states, and biomarkers of interest.
- TMA Analysis: Aarogyaline performs comprehensive analysis of TMA slides using techniques like immunohistochemistry (IHC) and fluorescence in situ hybridization (FISH) to quantify and localize biomarker expression patterns.
Follow up & Clinical Data Development
We can participate in projects and can provide all data of patients including 3 to 10 years follow-up
Quality Assurance :
All material have to as per Aarogyaline QA criteria :
- Subjects are recruited based strictly on the study’s inclusion/exclusion criteria.
- Written informed consent is required from all subjects participating in prospective collection studies before sample collection. Subjects receive a copy of the consent form, and the original is stored with the study records.
- Sample collection, processing, and shipment must adhere to the study protocol.
- Each specimen must be labeled and stored according to the study protocol.
- Data provided with each specimen must be complete, legible, and accurate.
- All subject information must be de-identified to protect privacy.
- Tissue specimens undergo review by Board Certified pathologists to confirm diagnosis, preservation method, specimen quality, and eligibility.