quarter Nick, and everyone. for morning, today results. you, our joining you good Thank for third Thank
not disruptions. had earlier we to resurgence to operations our Delta an the has as from through of year impact has have in the momentum these variant. strong due COVID-XX This on Our the learned continued despite manage
full of line the ahead XX% strong we end on longer XX% approvals remain finally, science XXXX, pipeline stage date XXXX. already of our Funding years industry starts continues for in which by unchanged. to drug are historically the September or launches. Our Association. exceeding run XXXX, high continues backdrop record the Venture almost and new And at of National are through continues Capital for of for X,XXX in up approved strong. billion high XX remains late-stage the with industry the Clinical FDA to levels year-to-date, of for The recent and is volume bullish $XX.X development. markets molecules Phase with with a IQVIA our drugs Phase year-to-year molecules an the at active keeping The starts over for the The to well particular. is over outlook bottom total are and in term set the the pace dynamics year levels commercial with of upcoming new XXXX strong, expand III and all-time XXXX. outlook to II very trending trial funding according Biotech be the life
And results York plans, will financial growth. conference well midterm line usual by the share which on of longer-term of outlook early to and of our for end our as Qs third next February. will review everyone with forward of we XX provide seeing driven stronger the above currency grew meeting, At investor we about was organic the quarter which, phase plans for of With in on our coinciding let's normally us The revenue time higher is the our growth. range. know, XX.X% margins by million November constant you $XX year join XX.X% think guidance basis at we for beat City. upcoming that, and you our midpoint and our XXXX, As was as the pass-throughs, and guidance can as ahead New look analyst then. I as want that our reported a remind you Revenue in somewhat hope and to primarily third We well dilutes quarter.
midpoint as EBITDA adjusted was due guidance range as our measures. well stronger beat XX.X%, above quarter Third $X performance. operational productivity growth the entirely reflecting to the revenue million of The grew our
with the Third quarter favorability guidance, the adjusted XX.X%. EBITDA midpoint below-the-line from the in EPS as diluted of of coming above as items. drop-through $X.XX adjusted That our $X.XX beat was grew well
now me provide business. an Let update the on
evidence in late decision-making, and role it real-world take In data and guidance FDA business on health electronic claims September, a health regulatory released can leading informing several their records care. continues how Our publications. support medical draft IQVIA the to cited
year trials, every With increases external provide and both therapies of context clinical the and the trials number growth studies single-arm important for rare payers. these driven of personalized competitors and medicine for disease regulators
area. our in Our this recognize expertise clients leading
major as long-term example, cardiovascular innovative guidance to And direct-to-patient top capture clients. IQVIA's this in In pharma a to external were requires of therapy. to a cell real-world follow-up a combining was IQVIA Regulatory a XX XX-year as example, awarded another for extended exposed recent an award. newly to and demonstrate effectiveness pivotal patients for gene technology we win deliver follow-up study well For had solutions and study we secondary the a capabilities comparator platforms safety therapy. data launched gene in
the to technology be the in marketplace. of offerings On front, our continue suite adopted
our You our OCE expand here. are we to with footprint continued And course, platform have, applications. of technology commercial and other familiar
wins very in quarter, adoption of date total we clinical the bringing the suite, number OCT. our are XX client to have XXX of We But OCE excited to increased customers. see new wins to trial orchestrated also
the XXX eCOA of platform experience portal across module, trials. biotechnology engagement and X,XXX for quarter, representing using module sites leading to selected active award-winning studies site our company XXX,XXX our now in bought site continues all This module. portal their have portal to a example, power Asia have that are that OCT within demand. Similarly, site strong We site our customers
deployed over XXX therapeutic this in The top using date, successfully including clients. has countries languages. customers areas. over have XX XX of To XX different platform, XX pharma processed over have unique and responses platform the projects XX X across XX We across patient million we
want I a industry. Now to about part our words say fast-growing a few of
with combined trials decentralized all capabilities, other and telemedicine several decentralized around including cancers decentralized The decentralized patient trial with and service trial OCT modules connected organized well familiar along platform. You're study nurses and including tech eCOA, as offering suite DCT. home our within coordinators, devices as or IQVIA our eConsent, our phlebotomists trial
ongoing active improve When to engagement over trial Importantly, XX trials clinical they are competitors offerings, totaling of DCT our utilize in patient with look business. areas, our over developed to we've and meaning find XX% patient of our speak trials. back XX diversity DCT decentralized or innovative including XX date XX and DCT different us. with billion. These clinical recruited trials we platform, run accelerate their decentralized trials own at of $X components which with XXX,XXX have therapeutic when trials fully are awards as in in about fully on inclusion and up look growing own step These recruitment their direct-to-patient and When DCT that actually one capabilities, sponsors, portfolio, XX services indications this unique at to is that more been importance often offerings, DCT unique XX we span our report the full-service of Incidentally, utilize our offering. we have we've countries. our trials patients awarded the multiple
combine a in space trials partner Our ability care and of advanced makes us the capabilities. with clinical of an and extensive chose to for investigators differentiates professionals utilize and full technology us this network decentralized
contracted of quarter, our Our $X.X net We continues $XX including and on build bookings September X.XX, pass-throughs; the pass-throughs. first overall for to approximately This bookings of contracted R&DS pass-throughs, LTM ratio business X.XX pass-throughs. the and LTM book-to-bill its including our including had strong excluding momentum. ratio new net X.XX billion new over in bringing pass-throughs. a net X.XX, in time was excluding book-to-bill At XX, to resulted billion
September to at grew Our year-over-year including contracted billion XX.X% pass-throughs, backlog in R&D, XXXX. XX, $XX.X
months our increased million revenue up second from sequentially quarter. a XX backlog $XXX to versus next $X.X billion, the As result,
lab expansion, we this will into several and the discovery times performance. These signaled announced We XXX,XXX new services it have I sponsors exploratory recently our in along the our now the Ron the to will of more capabilities, new and expansion top facility with genomics our in details of into on square the throughout of support comes bioanalytical, As closely services. facility quarter Carolina. moving foot cycle. in biomarker capabilities. vaccine customers to announced partner cutting-edge to investment enable in opening innovation in essential our life Scotland. And with North for over in provides to biomarkers past, on clinical laboratories ramped with access up new development XXX,XXX financial human course, we This foot last turn of molecules us an investments we've development square