Chembio three quarter to you today. continued execute for third the team during our The on of priorities us joining Thank XXXX. corporate
generated by total to impacted of during was quarter of product prior Africa compared lower period. the the third R&D Total sales year million, $X.X and revenue million. including sales revenue team in lower Our $X.X revenue
pleased in America impacts to on are significant we will product positive considerable recent business believe States, have Pacific. highlight and developments I'd our the forward. few sales However, in a the increases Asia with Latin United like that moving we
while flexibility dilution investment a grow by our capital million limiting business, the This Perceptive sheet In loan balance leading one to closing $XX world's firms. September, strengthened any to shareholders. care-focused we our provides our of Advisors, term health with
point-of-care will stock. XXX,XXX the $XXX,XXX state, of markets definitive common cash distributor the an acquire company today, held a the terms tests Under of The into enable in agreement infectious shares to Chembio's Earlier of agreement diseases. and pharmacy and of for Brazilian approximately Brazil. will make Orangelife, manufacturer acquisition private announced Chembio upfront expansion has signed privately that a and diagnostic commercial payment we
consulting include shares of regulatory common agreements XXX,XXX and Chembio certain XXXX enter Separately and that certain between sales of up to milestones achievement XXXX. payment into could on of stock, the based will additional
conditions, fourth of to is customary XXXX. acquisition, expected owned And the the quarter Chembio and a transaction be Orangelife renamed during subsidiary the operate Chembio. closing wholly following close to of Subject Diagnostics Brazil as as will
two important received Health WHO. by We approvals World the Organization,
supply manufacturing company First we our received STAT-PAK Malaysia WHO cost-effectively markets. international the and to approval Prequalification facility, allows HIV manufacture our of Malaysia in which tests
approval the Second, for we the expand our WHO which easiest of HIV prequalification use we CHECK SURE self-test allows is commercialization self-test, HIV received what to available. company believe to
a our entered company with develop Finally, pharmaceutical our can with into collaboration diagnostic platform utilize to undisclosed point-of-care reinforces and biomarker. test an second a we detect Takeda global a to This companion compatible quantitative or collaboration tests. represents portfolio belief of major a our to Pharmaceutical we build that
for today's call the expanding then our discussing additional pipeline; and for questions. quarter financial and growth. we'll three make commercialization; results, our call start few progress our preparing we'll Neil two, closing remarks on third advancing One, three, corporate On open review R&D Then a will by I'll priorities.
our expanding Starting commercialization. first our with priority,
States, an XXX% to Latin a and in the of increases quarter compared XXXX, During year United sales the prior product in of in a Asia. the XX% third a increase increase XX% significant had including number in regions increase period, America
timing Africa, benefited XXXX to which region. in Product and largely Europe ordering Middle which product by the and of the sales a by These attribute the decrease from increases acquisition opTricon. in offset in tenders in increased patterns were East, XX% XX% of we sales
notified of which during respective XXXX States, On We to of performance July third quarter the year compared its in not HIV chain prior main have nine sales technical would as and to first increased during the it's rapid an our estimate our distributors issue. and particularly that pleased did United supply XXX% the of one U.S. periods. when XX, with it XXXX, the customers competitors it to are months and XX% was and resolve test unable supply as its
they've On sent for "That in customers manufacturers experienced the U.S. and HIV issues." for memos orders of delivery Director production indicating Division "That of their their Centers resolve to companies test to diligently rapid Control CDC, tests." are working October XX, their of HIV both further have informed the Prevention HIV/AIDS two customers Disease Prevention, that And stated delays
rapid of a effective CDC presents increase tests. great further the three to Chembio to competitive other HIV products the to Chembio opportunity in FDA-approved And products. targeting them of is Chembio's including market, reminded sales U.S. HIV market. our customers This for U.S. accounts situation in the sales HIV available tests team convert CLIA-Waived
our our multiple grow expanding sales infectious including markets. in geographies through presence, global new We in entering confident registering commercial remain and disease drivers, ability to products new our
is SUS. a the system diagnostic Today's world's publicly for announcement with of an administered the and privately country Orangelife, acquire the known definitive world, expanding the agreement the has largest government-run ninth economy United or by largest our System, Brazil sixth step as company, GDP important business healthcare a and population. by in Health to held largest in Brazil,
Brazil's health the Fiocruz, for and a national which demands biopharmaceuticals, Foundation of and disease have to subsidiary Bio-Manguinhos of our with point-of-care production We development Ministry the Health in Oswaldo the federal the to products vaccines, sold products of diagnostics been XXXX, system. history of to is infectious long selling collaboration Cruz government. Chembio a public of have Brazil's Since responsible primarily meet
of the Health tests years, through infectious Ministry disease partner Brazil's last of we to supplied XX Over have millions our Bio-Manguinhos/Fiocruz.
most expand federal testing. Brazil in government. be why market to on Brazil? that an plan So for success infectious we've had the with by and building business in investment disease attractive make We consider the We our largest Brazil to the
reach channel. Brazil Those small XX,XXX pharmacies states unable hospitals X,XXX government private Brazil. the federal market for the through the include are that in XX,XXX outside retail that federal and responsible markets There are labs the government large markets which in market was includes Brazil, includes its that of Chembio in previously to
believe effective to to We the presence government access a Brazil, markets the physical federal way is country. in the have outside in most
With first Class of devices including Orangelife of facility Brazil, will IV the certified, to ISO medical approved we III acquisition have HIV GMP according a produce ANVISA and production self-test. in by the Brazil's ANVISA-approved that to is Brazil II
salespeople key success that a believe also having our Brazil We in own is factor.
calls, new multiplex dengue markets. distribution Brazil growth With chikungunya driver. Zika the acquisition, as test identified in salespeople network a access private On the we own and our for recent have a we'll state, and to and our future pharmacy
presence the health be all we complicates three country. to and and treatment valuable for is these Brazil believe for across which treatment. these stand-alone determine believe our We viruses, there tools In disease viruses significant products due need identification for tests care multiplex paths the will a of to outbreaks and professionals identify
is We further of Bio-Manguinhos for $XX our with products to we in We likelihood continue and the acquisition will annually orders of that Brazil believe opportunity million increase Health. success. approximately the Ministry from believe partner to the these work Orangelife secure of our
for million of call, one $X.X from chikungunya by last conditions the Zika mentioned our $X.X two one been contract Zika the contracts ranging contract multiplex to As to from UNICEF, team our million our million. test, test, working awarded million and $X.X meet dengue $X.X on for has ranging to
receive to related to initial that discussions and that contract our We're $X.X pleased confirmed related the I'm the Zika conditions meeting conditions for those included tests also order award that and a test. an in confirmed met evaluation test. purchase to we meeting we've will contract, work also we test report remain confident UNICEF all purchase to and and which conditions toward for receiving a million of order the the clinical that UNICEF Zika schedule with continue for delivery about the subsequent multiplex
Finally approval WHO significant Nations of company. make is used other driver the as agencies approval by decisions. standards and our self-testing CHECK United prequalification a Fund and signifies SURE the purchasing of safety The as HIV quality, WHO regulatory product growth PEPFAR, we international meets procurement performance for Global self-test that global and to a The and we Unitaid as the HIV pre-Q consider approval, view such
buffer HIV by ease required rapid The only solution device world's HIV XX The minutes. using design smallest and any required the collection blood CHECK test self-tests. capillary self-test use provides CHECK by devices sample the of unique results SURE eliminating buffer in bottles need SURE of separate and self-test provides HIV other unparalleled HIV for the solution, integrates and
HIV professionals. self-test HIV I HIV to and sensitivity users XXX% when which demonstrated CHECK SURE trained of The of detects II antibodies XX.X% comparing untrained HIV self-test specificity to and
HIV CHECK WHO The pre-qualified by professionals essential pre-qualified is is health marked, CE self-test I/II approved, that trusted the SURE newly CLIA-Waived, FDA Chembio's WHO the around HIV assay element globe. and care company's of
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Turning priority, R&D second our pipeline. to corporate advancing our
R&D we and multiple platform advancements affairs made During biomarkers. in numerous third point-of-care the across our in notably quarter regulatory
for test mark the of we quarter we CE As the CHECK the for fourth HIV noted prequalification this anticipate XXXX. self-test received earlier, WHO obtaining SURE and in
our for Administration Food We HIV the our the XXX(k) year-end test. approval multiplex and anticipate Zika U.S. and for approvals including test syphilis PMA approval before Drug BARDA-funded two
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all increased and R&D of results, development on our of advanced diagnostic sensitivity, which provide an focused multiplexing quantitative require is tests analyzer. Further, team that the
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advance to continue pharmaceutical of strategy technology point-of-care tests with our We to certain to to collaborating develop companies leverage biomarkers. identify our
we Takeda certain milestones. the quarter test signed the undisclosed be diagnostic with Takeda a third to terms develop will funding point-of-care the satisfying to Pharmaceuticals quantitative biomarker. agreement During subject by of for provided Under an an agreement,
to We expect December biomarkers Chembio's XXXX. to proprietary blood platform of end complete whole finger-stick in blood the using feasibility disease detect two by specific technology
test product In diagnostic identify first approval, AstraZeneca, both preclinical important point-of-care studies CE mark. collaboration completion with obtain regulatory the and we respiratory been view of we also and a as quantitative have completed eosinophilic disease milestones. and preclinicals a The successfully developed development the to
regulatory are optimistic design we work clinical FDA trials for about finalizing this approvals to of product, the toward continue and We additional including and achieving XXX(k). regulatory
us of consider were Finally opTricon acquisition previously platform adding biomarkers allows to that analyzer our to technology the the challenging.
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in of Perseus level continues capabilities the of test. to develop Our team provided detection we multiplexing those to including concussion collaboration the our are positioned including biomarkers by platform enhancement well evaluate a Due opTricon Science. analyzer, advanced numerous capabilities to with we believe concussion and point-of-care
our improving targets obtaining preparing objectives: growth. financial we're U.S. Malaysia several facilities achieve expanding WHO our for to additional To third Turning important our facilities. corporate our operational U.S. manufacturing pursuing our and prequalification for automating and priority
manufacturing increase to production capacity, increase efficiency strategy Our automation well U.S. is gross margins and designed flexibility. as as
manufacturing lines New We expect to York automated our achieve have facility by our objective three in year-end. to
is this and is delivered expected year-end Line production number be commenced to one be Line week tests three delivered be quarter of is expected this earlier We the first of number in operational on DPP operational two of the being and to XXXX. number quarter second line in XXXX. year. by
commenced to businesses. foot manufacturing So by U.S. our XXXX, locations growth. includes as operational will the all facility. This to all the improve facility to of capacity components our single facilities, expect a We for headquarters and multiple for be of XX,XXX and building corporate three square to serve which plan middle have house and we U.S. our additional lines expand U.S.
The is warehouse administrative, shipping first of three operating phases with in and complete facility new the functions planned all today.
which during Malaysia STAT-PAK allows manufacture quarter and test the fourth was markets, finalizing commencing HIV for international program planned the XXXX. approved subject research which STAT-PAK III, includes of supply quality by October of II, reached Phase which We company facility includes certain plans prequalification it in the in We're our to manufacturing Health a functions requirements. produce Organization to regulatory and XXXX the and tests. our completion for when manufacturing in development are both significant and which approval Phase World in milestone This are HIV to to we Malaysia,
facility, cost pursue sold way to will provide produce in of goods qualification for This our we be this future global the production business and tests capacity to opportunities to in this facility. expect production to and increase. Through paves reduced new other
to I'll details turn on it Neil Now, provide our to results. financial over