Important news about the Covid-19 testing benefit for the uninsured – click here

COVID-19 TESTING FOR ILLINOIS SCHOOLS

Achieve Health Management provides a seamless solution to support schools and other institutions in testing their students, faculty, staff, residents and employees for COVID-19.

Specimen Collection Kits, Collection Servicies, and Pre-Paid Overnight Shipping.

Results Reported in HIPAA-compliant Portal

48-Hour Turn Around Time

Billing & Reimbursement Services

About Achieve Health Management (AHM)

Achieve Health Management is a Clinical Services Company led by Principals with decades of innovative healthcare services experience across all channels and classes of trade.

SEAMLESS SOLUTION TO SUPPORT SCHOOLS

With the onset of COVID-19 in the US, Achieve and OSANG Healthcare, a South Korean manufacturer recognized globally for their high-quality molecular diagnostic products, medical devices, immunoassays and biochemicals, built a comprehensive solution to help the US healthcare market facilitate COVID-19 testing. OSANG Healthcare has provided tens of millions of test kits and worked with over 50 countries to provide COVID-19 testing solutions.

Achieve provides a seamless solution to support schools and other institutions in testing their students, faculty, staff, residents and employees for COVID-19. Achieve has a team of diagnostic experts, as well a CLIA-certified, nationwide laboratory network that analyzes multiple specimen types and reports results within 48 hours. Achieve diagnostic experts will coordinate the entire testing process on your behalf. Achieve Health has the capacity to administer and process high volume PCR testing.

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BENEFITS OF TESTING WITH AHM

Achieve Health Management fully manages end-to-end processes of on-site testing and provides proprietary registration, scheduling, and results reporting application.

NO COST

Billing and reimbursement to 3rd party payers offers no cost testing

LAB NETWORK

Priority overnight or couriered transportation of collected specimens to a CLIA-certified lab network and rapid results with a 48-hour turn around time from laboratory specimen receipt

EASE OF USE

All consent forms and other required documentation provided and trained medical staff performs on-site specimen collection

FDA AUTHORIZED

Achieve network laboratories conduct rtPCR molecular analysis with FDA_EUA approved COVID-19 test kits

MULTIPLE SPECIMEN TESTING

Multiple specimen and collection types available on-site and Rapid Antigen testing also available on-site

HIGH ACCURACY

Priority overnight or couriered transportation of collected specimens to a CLIA-certified lab network and rapid results with a 48-hour turn around time from laboratory specimen receipt

FAST RESULTS

Test results provided via HIPAA-secure online portal, secure email, SMS text or by phone with a 48-hour turn around time

EXTRACTION FREE PROTOCOL

Extraction free protocol accelerates COVID19 processing

Our Testing Services

Achieve Health Management provides comprehensive solutions for the range of COVID-19 testing needs.

Types Of Testing Available

Real Time PCR
Point Of Care Rapid Antigen
Over The Counter Rapid Antigen

Specimen Collection Services

Collection kit shipment to facilities (Nasopharyngeal swabs, Oropharyngeal swabs, Anterior nares swabs and rapid Antigen tests)
Pre-paid shipping labels provided
Contracted medical staff to collect specimens (can be arranged by individual facility if needed)
Third party payer reimbursement for testing and specimen collection services

ACHIEVE Advantages

Rapid results 48-hour turn around time from laboratory specimen reciept
Extraction free protocol accelerates COVID 19 processing through put
Confidence in test results to protect test population & staff
Protected health information via HIPAA-compliant portal & reporting
Achieve manages end-to-end processes, including billing & reimbursement

This test is only authorized for use in CLIA-certified laboratories that meet requirements for high complexity tests. This test has not been FDA cleared or approved. This test has been authorized by FDA under and EUA for use by authorized laboratories. This test has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens. This test is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of thet Act, 21 U.S.C. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner (Section IV(BB)).

2211 Encinitas Blvd, Ste 200, Encinitas, CA 92024