Medics Connect Ltd. Company was established in Yemen, as a specialized company to provide TeleHealth solutions. Medics Connect Ltd. Co. is capable of processing and overcoming a wide range of challenges and health problems through using modern technology radiology and writing medical reports remotely around the clock (24 hours) throughout the year with consultation and guidance by the senior consultants in the field of radiology in Yemen.
The company is also distinguished by developing tailor-made solutions to suit the needs of the community in the best quality of time with affordable prices.
Healthcare providers access vRad’s network of 500 radiologists – most of whom are subspecialty trained – at any time of day, from any location. Our radiologists practice on the industry’s most advanced, fully-integrated technology and support platform that vRad built and has been perfecting for remote radiology since 2001.
QA program emphasizing performance improvement since 2004
Average turnaround time for stroke studies
Yemen-based operations and technical support center
vRad team members and radiologists collaborate to develop life-saving technologies such as artificial intelligence prioritization for critical cases. Our long history of continuous innovation enables all vRad radiologists to read at the top of their license and deliver faster, higher-quality results for patients in urgent need of care.
Medices Connect® has gone through rigorous testing and evaluations of various compliance authorities. It is the constant endeavor of the team to keep the product within compliance guidelines and add new features to suit the market needs.
The product is approved by the FDA and CE authorities. The studies are also stored in a datacenter which is replicated at a disaster management location. The data center has been certified according to the SAS 70 Type II & SSAE 16/SOC 1 (The “New” SAS 70) requirements. This exceeds the stringent standards for security and operations that Sarbanes-Oxley, HIPAA, Gramm-Leach- Bliley and other regulations require.
FDA (Food and Drug Administration) is a government agency responsible for the safety of food, dietary supplements, human drugs, vaccines, blood products and other biologicals, medical devices, radiation-emitting electronics, cosmetics, veterinarian products and tobacco products being sold or manufactured in the United States.
Organizations that manufacture, re-pack or re-label products in the aforementioned industries must register with the FDA, except for cosmetics, where registration is voluntary.
CE marking is a certification mark that indicates conformity with health, safety, and environmental protection standards for products sold within the European Economic Area (EEA). The CE marking is also found on products sold outside the EEA that are manufactured in, or designed to be sold in, the EEA. This makes the CE marking recognizable worldwide even to people who are not familiar with the European Economic Area.
According to the U.S. Department of Health and Human Services (HHS), the HIPAA Privacy Rule, or Standards for Privacy of Individually Identifiable Health Information, establishes national standards for the protection of certain health information. Additionally, the Security Rule establishes a national set of security standards for protecting specific health information that is held or transferred in electronic form. Our datacenter has just passed a rigorous HIPAA Compliance Risk Assessment and met every requirement set forth by the U.S. Department of Health & Human Services.