Healthcare Software
Development Services

As a leading custom healthcare software development company, we leverage FHIR compliance to embrace compatibility in the healthcare industry, fostering smooth collaboration between various healthcare organizations and enhancing patient care coordination.

As a part of our custom software development services, we comply with CPT to expedite the billing and coding process, ensuring efficient payment for medical services and simplifying documentation for healthcare practitioners.

We comply with GxP regulations to maintain the highest quality standards in developing healthcare products. The integrity and safety of medications, medical devices, and clinical trials are guaranteed by GxP guidelines, which cover Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and Good Clinical Practice (GCP).

EU Annex 11 compliance allows us to navigate the regulatory landscape of Europe confidently. In order to ensure data integrity, security, and compliance with EU rules, this standard lays out standards for using computerized systems in regulated contexts.

As a pioneering provider of custom healthcare software development services, we adhere to CDISC to improve the interoperability and integrity of clinical research data by maintaining uniformity in data collection, processing, and reporting through adherence to CDISC standards.

XDS/XDS-I compliance enables smooth electronic health record sharing amongst healthcare organizations. This standard improves interoperability by fostering effective and safe data interchange and facilitates better decision-making and patient care coordination.

As a top provider of custom healthcare software development services, we strictly adhere to SSAE compliance standards to prioritize the security and legality of your healthcare services, ensuring that your stakeholders receive the highest level of data privacy at every level.

As a top-tier healthcare software development company, we implement stringent security measures by ensuring that your team can leverage the benefits of BYOD without compromising on the security and integrity of sensitive healthcare information

As a leading provider of software development services for healthcare, we adhere to the strict regulatory standards set by the FDA (Food and Drug Administration) which includes thorough documentation, rigorous testing, and complying with Good Manufacturing Practices (GMP) wherever applicable.

As an exceptional healthcare software development agency, we abide by the highest standards of confidentiality and data security set by HIPAA (Health Insurance Portability and Accountability Act), which also encompasses stringent access control measures and encryption protocols.

Every healthcare software that we develop abides by the HITECH Act. Being a top-ranked medical software development company, we ensure that your custom-built healthcare software successfully passes all the security audits that are made to ensure strict enforcement of the HITECH-based privacy and security rules.

As a renowned medical software development company, we follow the concepts and SaMD risk categories detailed by the International Medical Device Regulators Forum for the medical software development industry, ensuring the highest standards of safety and reliability in our software.

We follow the set of international standards for sharing, exchanging, integrating, and retrieving healthcare information as dictated by the Health Level 7 organization. Our commitment to adhering to these standards ensures efficiency in healthcare data management.

Our data collection and management process is designed to follow all the stringent GDPR compliance requirements. By adhering to the GDPR rules, we ensure that every data that your application works with is highly secure.

A globally-renowned medical software development company like ours abides by SOC 2 compliance, ensuring the greatest levels of security and privacy for your medical records. This framework is centered on protecting client data and guaranteeing the privacy and accuracy of sensitive medical records at every stage.

Complying with PHIPA is paramount for healthcare providers in Ontario to acquire, use, and securely disclose personal health information. We adhere to PHIPA to ensure patient data privacy and confidentiality, which promotes patients’ confidence in healthcare services.

We adhere to DICOM compliance to integrate the software with medical imaging systems smoothly. This standard ensures accuracy and interoperability in healthcare diagnosis and treatment planning by facilitating the standardization of medical imaging data interchange and management.

As a leading custom healthcare software development company, we leverage FHIR compliance to embrace compatibility in the healthcare industry, fostering smooth collaboration between various healthcare organizations and enhancing patient care coordination.

As a part of our custom software development services, we comply with CPT to expedite the billing and coding process, ensuring efficient payment for medical services and simplifying documentation for healthcare practitioners.

We comply with GxP regulations to maintain the highest quality standards in developing healthcare products. The integrity and safety of medications, medical devices, and clinical trials are guaranteed by GxP guidelines, which cover Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and Good Clinical Practice (GCP).

EU Annex 11 compliance allows us to navigate the regulatory landscape of Europe confidently. In order to ensure data integrity, security, and compliance with EU rules, this standard lays out standards for using computerized systems in regulated contexts.