Medical Coding
Medical Coding is the process of translating complex clinical documentation into standardized medical codes used for data reporting, billing, and regulatory submissions. It ensures the accuracy, consistency, and compliance of clinical and healthcare data throughout the research process. By converting medical terms, diagnoses, procedures, and drugs into recognized global code sets such as ICD, CPT, MedDRA, and WHO-DD, medical coding enables seamless communication between researchers, sponsors, and regulatory authorities. This structured approach enhances data clarity, supports better analysis, and ensures that all medical information is globally interpretable and compliant.
At UNIFIED POINTS TECH, we deliver precise and reliable medical coding services designed to maintain the integrity and quality of your clinical data. Our expert coding team ensures every clinical term is accurately classified, verified, and validated according to international standards. We focus on achieving full regulatory compliance, reducing data discrepancies, and improving the overall efficiency of clinical operations. Through our robust coding practices, UNIFIED POINTS TECH helps clients enhance study accuracy, streamline submissions, and strengthen confidence in their clinical research outcomes.
Inpatient and Outpatient Coding
Our Inpatient and Outpatient Coding services at Microline Information Systems ensure accurate and detailed coding for all types of hospital stays and outpatient visits. We cover a broad spectrum of medical specialties, enabling healthcare providers to document patient care precisely. This accuracy is crucial for proper billing, insurance claims, and regulatory compliance. Our expert coders stay updated with the latest coding guidelines to reduce errors and avoid claim denials. By handling both inpatient and outpatient cases, we support seamless revenue cycle management.
We understand that inpatient coding involves more complex documentation due to longer hospital stays and multiple procedures, while outpatient coding requires quick turnaround and precision. Our team is skilled in managing both scenarios efficiently without compromising quality. We tailor our services to meet the specific needs of your healthcare facility, ensuring all patient encounters are coded correctly. With Microline Information Systems, you can expect timely, compliant, and reliable coding support that enhances your operational workflow. Our commitment is to accuracy, consistency, and maximizing reimbursement potential.
Adverse Event (AE) Coding
Adverse Event (AE) Coding is a critical process in clinical research that involves coding all adverse events reported during a study using standardized medical terminology. At UNIFIED POINTS TECH, we utilize the MedDRA (Medical Dictionary for Regulatory Activities) standards to ensure each event is classified consistently and accurately. This enables clear communication of safety data across sponsors, regulatory authorities, and research teams. Our systematic approach ensures that all adverse events are captured, coded, and analyzed effectively to identify safety patterns and potential risks.
The expert team at UNIFIED POINTS TECH performs detailed reviews of clinical documentation to ensure every reported event aligns with the correct MedDRA hierarchy. This process supports transparent and reliable safety reporting for both interim analyses and final regulatory submissions. By maintaining coding consistency and compliance across all study phases, we help clients strengthen pharmacovigilance practices, enhance data accuracy, and meet global regulatory expectations with confidence.
Lab Test Coding
Lab Test Coding is an essential component of clinical data standardization that ensures laboratory test results are uniformly classified and interpreted across multiple studies. At UNIFIED POINTS TECH, we accurately code all laboratory tests using globally recognized terminologies and standard dictionaries such as LOINC and MedDRA. This process guarantees that lab data is represented consistently, regardless of study site or laboratory source. By maintaining uniform coding standards, we enable seamless data integration and analysis across global clinical trials.
Our skilled coding team at UNIFIED POINTS TECH ensures that each lab parameter is mapped precisely to the correct terminology and validated for regulatory compliance. This standardized approach improves data quality, facilitates accurate comparisons between studies, and supports efficient regulatory submissions. Through our meticulous coding and validation process, we help sponsors achieve higher data reliability, faster reviews, and a stronger foundation for informed clinical and safety decisions.
