• Live Feeds
    • Press Releases
    • Insider Trading
    • FDA Approvals
    • Analyst Ratings
    • Insider Trading
    • SEC filings
    • Market insights
  • Analyst Ratings
  • Alerts
  • Subscriptions
  • Settings
  • RSS Feeds
Quantisnow Logo
  • Live Feeds
    • Press Releases
    • Insider Trading
    • FDA Approvals
    • Analyst Ratings
    • Insider Trading
    • SEC filings
    • Market insights
  • Analyst Ratings
  • Alerts
  • Subscriptions
  • Settings
  • RSS Feeds
PublishGo to App
    Quantisnow Logo

    © 2026 quantisnow.com
    Democratizing insights since 2022

    Services
    Live news feedsRSS FeedsAlertsPublish with Us
    Company
    AboutQuantisnow PlusContactJobsAI superconnector for talent & startupsNEWLLM Arena
    Legal
    Terms of usePrivacy policyCookie policy

    AstraZeneca results: Q1 2026

    4/29/26 7:00:00 AM ET
    $AZN
    Biotechnology: Pharmaceutical Preparations
    Health Care
    Get the next $AZN alert in real time by email

    Strong revenue growth and positive readouts from high-value NMEs reinforce confidence in 2030 ambition

    AstraZeneca:

    Revenue and EPS summary

     

    Q1 2026

    % Change

     

    $m

    Actual

    CER1

    - Product Sales

    14,386

    12

    7

    - Alliance Revenue

    825

    29

    26

    Product Revenue

    15,211

    13

    8

    Collaboration Revenue

    77

    4

    -

    Total Revenue

    15,288

    13

    8

    Reported EPS ($)

    1.99

    6

    8

    Core2 EPS ($)

    2.58

    4

    5

    Key performance elements for Q1 2026

    (Growth numbers at constant exchange rates)

    • Total Revenue up 8% to $15,288m, driven by double‑digit growth in Oncology and Rare Disease
    • Core Operating profit increased 12%
    • Core EPS growth of 5%, reflecting the favourable tax rate in the prior year period
    • Core Tax rate of 21%. Expectations for full year Core Tax rate are unchanged at 18-22%
    • Positive readouts for four high-value Phase III programmes since Q4 2025 results, including for two NMEs: tozorakimab and efzimfotase alfa
    • 14 approvals in major regions since Q4 2025 results

    Pascal Soriot, Chief Executive Officer, AstraZeneca, said:

    "We delivered strong growth in Q1 2026, with Total Revenue above $15 billion, demonstrating our consistent commercial execution. We are advancing through our catalyst‑rich period, with positive readouts for four high-value Phase III programmes since our last quarterly results, including first pivotal data for two key NMEs - tozorakimab in COPD and efzimfotase alfa in hypophosphatasia.

    We continue to invest in our commercial capabilities as we prepare for multiple launches, look forward to further readouts anticipated this year, and remain on track to achieve our ambition for 2030 and beyond."

    Guidance

    AstraZeneca reconfirms Total Revenue and Core EPS guidance3 for FY 2026 at CER, based on the average foreign exchange rates through 2025.

    Total Revenue is expected to increase by a mid-to-high single-digit percentage

    Core EPS is expected to increase by a low double-digit percentage

    The Core Tax rate is expected to be between 18-22%

    If foreign exchange rates for April 2026 to December 2026 were to remain at the average rates seen in March 2026, it is anticipated that Total Revenue in FY 2026 would benefit from a low single-digit percentage positive impact (unchanged) compared to the performance at CER, and Core EPS growth would be broadly similar (unchanged) to the growth at CER.

    Results highlights

    Table 1: Milestones achieved since the prior results announcement

    Phase III and other registrational data readouts

    Medicine

    Trial

    Indication

    Event

    Imfinzi

    EMERALD-3

    Locoregional HCC

    Primary endpoint met

    Imfinzi + Orpathys

    SAMETA

    MET+ advanced papillary renal cell carcinoma

    Primary endpoint not met

    tozorakimab

    OBERON

    COPD

    Primary endpoint met

    tozorakimab

    TITANIA

    COPD

    Primary endpoint met

    tozorakimab

    MIRANDA

    COPD

    Primary endpoint met

    tozorakimab

    PROSPERO

    COPD

    Primary endpoint not met

    Breztri

    ATHLOS

    COPD

    Primary endpoint met

    efzimfotase alfa

    MULBERRY

    HPP (paediatric, treatment-naïve)

    Primary endpoint met

    efzimfotase alfa

    CHESTNUT

    HPP (paediatric, switch from Strensiq)

    Primary endpoint met

    efzimfotase alfa

    HICKORY

    HPP (adults, adolescents, treatment-naïve)

    Primary endpoint not met

    Ultomiris

    I CAN

    IgAN

    Primary endpoint met

    Ultomiris

    ARTEMIS

    CSA-AKI

    Discontinued due to inconsistent efficacy

    Regulatory approvals

    Medicine

    Trial

    Indication

    Region

    Calquence

    AMPLIFY

    1L CLL (fixed duration)

    US

    Enhertu

    DESTINY-Gastric04

    2L HER2+ gastric/GEJ cancer

    JP

    Enhertu

    DESTINY-PanTumor02

    HER2-positive solid tumours

    JP

    Enhertu

    DESTINY-Breast11

    Neoadjuvant HER2+ Stage II or III breast cancer

    CN

    Imfinzi

    MATTERHORN

    Resectable gastric/GEJ cancer

    EU

    Imfinzi

    HIMALAYA

    1L HCC

    CN

    Imfinzi

    POSEIDON

    1L NSCLC

    CN

    Breztri

    KALOS / LOGOS

    Asthma

    US

    Saphnelo

    TULIP-SC

    SLE (subcutaneous)

    JP, US

    Tezspire

    WAYPOINT

    Chronic rhinosinusitis with nasal polyps

    JP, CN

    Tezspire

    DIRECTION

    Severe asthma

    CN

    Koselugo

    KOMET

    Adult NF1-PN

    CN

    Regulatory submissions or acceptances* in major regions

    Medicine

    Trial

    Indication

    Region

    Calquence

    AMPLIFY

    1L CLL (fixed duration)

    JP

    Calquence

    ECHO

    1L MCL

    CN

    Enhertu

    DESTINY-Breast05

    High-risk HER2+ early breast cancer (post-neoadjuvant)

    US, EU, JP, CN

    Enhertu

    DESTINY-PanTumor03

    HER2-expressing solid tumours

    CN

    Datroway

    TROPION-Breast02

    1L TNBC for patients where immunotherapy is not an option

    JP

    baxdrostat

    BaxHTN / Bax24 / BaxAsia

    Treatment resistant hypertension

    CN

     

    * US, EU and China regulatory entries in this table denote filing acceptance

    Other pipeline updates

    For recent trial starts and anticipated timings of key trial readouts, please refer to the Clinical Trials Appendix document in the financial results section of the AstraZeneca investor relations website: www.astrazeneca.com/investor-relations.html

    Table 2: Key elements of financial performance: Q1 2026

    For the quarter

    Reported

    Change

    Core

    Change

     

    ended 31 March

    $m

    Act

    CER

    $m

    Act

    CER

     

    Product Revenue

    15,211

    13

    8

    15,211

    13

    8

    * See Tables 3, 7, 25 and 26 for further details of Product Revenue, Product Sales and Alliance Revenue

    Collaboration Revenue

    77

    4

    -

    77

    4

    -

    * See Tables 4 and 27 for further details of Collaboration Revenue

    Total Revenue

     

    15,288

    13

    8

    15,288

    13

    8

    * See Tables 5 and 6 for Total Revenue by Therapy Area and by region

    Gross Margin (%)

    82

    -1pp

    +1pp

    83

    -1pp

    +1pp

    * Variations in Gross Margin can be expected between periods due to various factors, including fluctuations in foreign exchange rates, product seasonality and Collaboration Revenue

    R&D expense

    3,492

    11

    7

    3,461

    12

    8

    * Core R&D: 23% of Total Revenue

    + Accelerated recruitment in ongoing trials

    + Investments in transformative technologies such as IO bispecifics, cell therapy and antibody drug conjugates

    + Addition of R&D projects from business development

    + Positive data readouts for high value pipeline opportunities that have ungated large late-stage trials

    SG&A expense

    4,920

    10

    6

    3,859

    12

    7

    * Core SG&A: 25% of Total Revenue

    + Investment to support ongoing and future launches

    Other operating income and expense4

    189

    67

    65

    189

    65

    63

    + Various partner milestones

    Operating profit

    4,246

    16

    17

    5,352

    11

    12

     

    Operating Margin (%)

    28

    +1pp

    +2pp

    35

    -

    +1pp

     

    Net finance expense

    320

    20

    16

    281

    30

    26

    + Prior year Net finance expense benefitted from adjustments relating to settlements with tax authorities

    Tax rate (%)

    21

    +7pp

    +7pp

    21

    +5pp

    +5pp

    * Prior year benefitted from the release of tax liabilities following settlements with tax authorities

    * Variations in the tax rate can be expected between periods

    EPS ($)

    1.99

    6

    8

    2.58

    4

    5

     

    For dollar values in this table, the unit of change is percent. For Gross Margin, Operating Margin and Tax rate, the unit of change is percentage points (pp).

     

    In the table above, R&D expense, SG&A expense and Net finance expense are displayed as positive numbers. The plus and minus symbols next to comments denote the directional impact of the item being discussed. For example, a plus symbol next to a comment about an R&D item indicates that the item increased R&D expenditure relative to the prior year period.

    Corporate and business development

    Jacobio Pharma

    In March 2026, Jacobio Pharma announced that it had received an upfront payment of $100m from AstraZeneca. The payment was made in accordance with the collaboration and license agreement announced in December 2025 for JAB‑23E73, an investigational oral pan‑KRAS inhibitor.

    Pinetree

    In April 2026, AstraZeneca exercised its option to obtain an exclusive global license from Pinetree Therapeutics, Inc. (Pinetree) to develop and commercialize PTX-299, a first-in-class bispecific antibody degrader targeting EGFR. The option exercise triggers a $25m payment to Pinetree. Pinetree is also eligible to receive potential future development, regulatory, and commercial milestone payments and tiered royalties on global net sales if the product is successfully developed and commercialized. The total potential value of the agreement exceeds $500m.

    CSPC

    In April 2026, AstraZeneca closed the previously announced new strategic collaboration agreement with CSPC Pharmaceuticals to advance the development of multiple next-generation therapies for obesity and type 2 diabetes. AstraZeneca will pay an upfront payment of $1.2bn. See Note 5 for further details.

    Sustainability highlights

    The Company released its third Sustainability Impact Publication which includes its Sustainability achievements to date, updated 2030 Sustainability targets and case studies from across the enterprise on climate and nature action, health equity and health systems resilience.

    Reporting calendar

    The Company intends to publish its H1 and Q2 2026 results on 27 July 2026.

    Conference call

    A conference call and webcast for investors and analysts will begin today, 29 April 2026, at 14:30 UK time. Details can be accessed via astrazeneca.com.

    Reporting changes since FY 2025

    The therapy area formerly referred to as ‘Vaccines and Immune Therapies' is now titled ‘Infectious Disease'.

    The updated title aligns with the naming convention of AstraZeneca's other therapy areas, which are named after the scientific fields in which they operate

    Notes

    1. Constant exchange rates. The differences between Actual Change and CER Change are due to foreign exchange movements between periods in 2026 vs. 2025. CER financial measures are not accounted for according to generally accepted accounting principles (GAAP) because they remove the effects of currency movements from Reported results.
    2. Core financial measures are adjusted to exclude certain items. The differences between Reported and Core measures are primarily due to costs relating to the amortisation of intangibles, impairments, legal settlements and restructuring charges. A full reconciliation between Reported EPS and Core EPS is provided in Table 10 in the Financial Performance section of this document.
    3. The Company is unable to provide guidance on a Reported basis because it cannot reliably forecast material elements of the Reported results, including any fair value adjustments arising on acquisition-related liabilities, intangible asset impairment charges and legal settlement provisions. Please refer to the Cautionary statements section regarding forward-looking statements at the end of this announcement.
    4. Income from disposals of assets and businesses, where the Group does not retain a significant ongoing economic interest, is recorded in Other operating income and expense in the Group's financial statements.

    To read AstraZeneca's Q1 2026 Financial Results press release in full, click here.

    View source version on businesswire.com: https://www.businesswire.com/news/home/20260428491257/en/

    Global Media Relations team

    global-mediateam@astrazeneca.com

    +44 (0)1223 344 800

    Get the next $AZN alert in real time by email

    Crush Q1 2026 with the Best AI Superconnector

    Stay ahead of the competition with Standout.work - your AI-powered talent-to-startup matching platform.

    AI-Powered Inbox
    Context-aware email replies
    Strategic Decision Support
    Get Started with Standout.work

    Recent Analyst Ratings for
    $AZN

    DatePrice TargetRatingAnalyst
    1/27/2026Buy
    Citigroup
    10/27/2025Buy
    Jefferies
    10/16/2025Hold → Sell
    Deutsche Bank
    4/15/2025$75.00Outperform
    Exane BNP Paribas
    2/13/2025Neutral → Buy
    UBS
    2/12/2025Overweight
    Morgan Stanley
    11/20/2024Sell → Neutral
    UBS
    11/6/2024Sell → Hold
    Deutsche Bank
    More analyst ratings

    $AZN
    Press Releases

    Fastest customizable press release news feed in the world

    View All

    Camizestrant Combination Delayed Time to First Progression by 55% and to Second Progression by 37% in Patients With Advanced HR-positive Breast Cancer With an Emergent ESR1 Tumor Mutation in SERENA-6 Trial

    Switching to camizestrant led to a 99% median reduction in total ctDNA vs. a 64% increase for patients who remained on standard of care 51% of patients receiving the camizestrant combination achieved total ctDNA clearance vs. 1.9% with standard of care – early total ctDNA clearance was associated with an improvement in long-term outcome Further positive results from the Phase III SERENA-6 trial showed AstraZeneca's camizestrant plus a cyclin-dependent kinase (CDK) 4/6 inhibitor – palbociclib, ribociclib or abemaciclib – maintained its progression-free survival (PFS) benefit with longer follow-up and delivered a statistically significant and clinically meaningful improvement in second pr

    6/2/26 8:00:00 AM ET
    $AZN
    Biotechnology: Pharmaceutical Preparations
    Health Care

    IMFINZI® (durvalumab) plus IMJUDO® (tremelimumab-actl) combined with lenvatinib and TACE reduced the risk of disease progression or death by 30% in embolization-eligible unresectable liver cancer in EMERALD-3 Phase III trial

    Positive overall survival trend in favor of STRIDE regimen with lenvatinib and TACE Positive results from the EMERALD-3 Phase III trial showed AstraZeneca's IMFINZI® (durvalumab) in combination with IMJUDO® (tremelimumab-actl), lenvatinib and transarterial chemoembolization (TACE), demonstrated a statistically significant and clinically meaningful improvement in progression-free survival (PFS) versus TACE alone for patients with unresectable hepatocellular carcinoma (HCC) eligible for embolization. Patients in the investigational arms were treated with the STRIDE regimen (Single Tremelimumab-actl Regular Interval Durvalumab), with or without lenvatinib, prior to TACE and then in combinati

    6/1/26 8:00:00 AM ET
    $AZN
    Biotechnology: Pharmaceutical Preparations
    Health Care

    IMFINZI® (durvalumab) approved in the US in first and only immunotherapy combination for patients with BCG-naïve, high-risk non-muscle-invasive bladder cancer

    Based on POTOMAC Phase III trial results which showed a 32% reduction in the risk of high-risk disease recurrence, progression or death after one year of IMFINZI added to BCG vs. BCG alone AstraZeneca's IMFINZI® (durvalumab) in combination with Bacillus Calmette-Guérin (BCG) induction and maintenance therapy has been approved in the US for the treatment of adult patients with BCG-naïve, high-risk non-muscle-invasive bladder cancer (NMIBC). The approval by the Food and Drug Administration (FDA) is based on positive results from the POTOMAC Phase III trial which were presented at the European Society for Medical Oncology (ESMO) Congress 2025 and simultaneously published in The Lancet. I

    5/28/26 9:18:00 PM ET
    $AZN
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $AZN
    SEC Filings

    View All

    SEC Form 6-K filed by AstraZeneca PLC

    6-K - ASTRAZENECA PLC (0000901832) (Filer)

    6/1/26 10:10:07 AM ET
    $AZN
    Biotechnology: Pharmaceutical Preparations
    Health Care

    SEC Form 6-K filed by AstraZeneca PLC

    6-K - ASTRAZENECA PLC (0000901832) (Filer)

    6/1/26 10:06:30 AM ET
    $AZN
    Biotechnology: Pharmaceutical Preparations
    Health Care

    SEC Form 6-K filed by AstraZeneca PLC

    6-K - ASTRAZENECA PLC (0000901832) (Filer)

    5/29/26 6:43:39 AM ET
    $AZN
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $AZN
    Analyst Ratings

    Analyst ratings in real time. Analyst ratings have a very high impact on the underlying stock. See them live in this feed.

    View All

    Citigroup initiated coverage on AstraZeneca

    Citigroup initiated coverage of AstraZeneca with a rating of Buy

    1/27/26 8:43:14 AM ET
    $AZN
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Jefferies resumed coverage on AstraZeneca

    Jefferies resumed coverage of AstraZeneca with a rating of Buy

    10/27/25 8:41:53 AM ET
    $AZN
    Biotechnology: Pharmaceutical Preparations
    Health Care

    AstraZeneca downgraded by Deutsche Bank

    Deutsche Bank downgraded AstraZeneca from Hold to Sell

    10/16/25 8:19:10 AM ET
    $AZN
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $AZN
    Insider Trading

    Insider transactions reveal critical sentiment about the company from key stakeholders. See them live in this feed.

    View All

    Officer Sharma Mani sold $2,209,482 worth of Ordinary Shares (11,893 units at $185.78), decreasing direct ownership by 38% to 19,262 units (SEC Form 4)

    4 - ASTRAZENECA PLC (0000901832) (Issuer)

    5/22/26 4:05:16 PM ET
    $AZN
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Officer Sharma Mani was granted 2 units of Ordinary Shares, increasing direct ownership by 0.01% to 31,155 units (SEC Form 4)

    4 - ASTRAZENECA PLC (0000901832) (Issuer)

    5/8/26 4:05:20 PM ET
    $AZN
    Biotechnology: Pharmaceutical Preparations
    Health Care

    SEC Form 3 filed by new insider Sharma Mani

    3 - ASTRAZENECA PLC (0000901832) (Issuer)

    3/19/26 7:51:36 PM ET
    $AZN
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $AZN
    Financials

    Live finance-specific insights

    View All

    BAXFENDY approved in the US as the first and only aldosterone synthase inhibitor treatment for adults with hypertension

    Approval based on BaxHTN Phase III results showing statistically significant and clinically meaningful reduction in systolic blood pressure in patients with uncontrolled or resistant hypertension BAXFENDY 2mg lowered systolic blood pressure by 15.7 mmHg (9.8 mmHg placebo-adjusted) from baseline in BaxHTN trial AstraZeneca's BAXFENDY™ (baxdrostat) has been approved in the US as a first-in-class aldosterone synthase inhibitor (ASI) for the treatment of hypertension in combination with other antihypertensive medications, to lower blood pressure in adults who are not adequately controlled. This press release features multimedia. View the full release here: https://www.businesswire.com/news

    5/18/26 7:00:00 AM ET
    $AZN
    Biotechnology: Pharmaceutical Preparations
    Health Care

    AstraZeneca results: Q1 2026

    Strong revenue growth and positive readouts from high-value NMEs reinforce confidence in 2030 ambition AstraZeneca: Revenue and EPS summary   Q1 2026 % Change   $m Actual CER1 - Product Sales 14,386 12 7 - Alliance Revenue 825 29 26 Product Revenue 15,211 13 8 Collaboration Revenue 77 4 - Total Revenue 15,288 13 8 Reported EPS ($) 1.99 6 8 Core2 EPS ($) 2.58 4 5 Key performance elements for Q1 2026 (Growth numbers at constant exchange rates) Total Revenue

    4/29/26 7:00:00 AM ET
    $AZN
    Biotechnology: Pharmaceutical Preparations
    Health Care

    AstraZeneca results: FY and Q4 2025

    Strong commercial performance and excellent pipeline delivery in a continuing catalyst-rich period AstraZeneca: Revenue and EPS summary   FY 2025 % Change Q4 2025 % Change   $m Actual CER1 $m Actual CER - Product Sales 55,573 9 9 14,538 9 7 - Alliance Revenue 3,067 39 38 959 34 33 Product Revenue2 58,640 10 10 15,497 10 8 Collaboration Revenue 99 (89) (89) 6 (99) (99) Total Revenue 58,739 9 8 15,503 4

    2/10/26 7:00:00 AM ET
    $AZN
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $AZN
    Leadership Updates

    Live Leadership Updates

    View All

    Walmart Inc. to Join the Nasdaq-100 Index® Beginning January 20th, 2026

    NEW YORK, Jan. 09, 2026 (GLOBE NEWSWIRE) -- Nasdaq (NASDAQ:NDAQ) today announced that Walmart Inc. (NASDAQ:WMT), will become a component of the Nasdaq-100 Index® (NDX®), the Nasdaq-100 Equal Weighted™ Index (NDXE™), and the Nasdaq-100 Ex-Tech Sector™ Index (NDXX™) prior to market open on Tuesday, January 20, 2026 - the first trading day following the third Friday of the month. Walmart Inc. will replace AstraZeneca PLC (NASDAQ:AZN) in the Nasdaq-100 Index®, the Nasdaq-100 Equal Weighted Index, and the Nasdaq-100 Ex-Tech Sector Index. AstraZeneca PLC will also be removed from the Nasdaq-100 ESG™ Index (NDXESG™), Nasdaq-100 ex Top 30™​ (NDX70™), Nasdaq-100 ex Top 30​ UCITS™ (NDX70U™), Nasdaq

    1/9/26 8:00:00 PM ET
    $AZN
    $NDAQ
    $WMT
    Biotechnology: Pharmaceutical Preparations
    Health Care
    Investment Bankers/Brokers/Service
    Finance

    Vistagen Appoints Nick Tressler as Chief Financial Officer

    Vistagen (NASDAQ:VTGN), a late clinical-stage biopharmaceutical company pioneering neuroscience with nose-to-brain neurocircuitry to develop and commercialize a new class of intranasal product candidates called pherines, today announced the appointment of Nick Tressler as Chief Financial Officer (CFO), effective today, December 1, 2025. "I am excited to welcome Nick to Vistagen as our CFO. His financial and strategic acumen and extensive operational experience in the biopharmaceutical industry will be instrumental as we accelerate into our next phase," said President and Chief Executive Officer of Vistagen, Shawn Singh. "I look forward to his contributions to our leadership team and the po

    12/1/25 8:30:00 AM ET
    $AZN
    $SENS
    $VTGN
    Biotechnology: Pharmaceutical Preparations
    Health Care
    Medical/Dental Instruments

    I-Mab Appoints Phillip Dennis, MD, PhD, as Chief Medical Officer

    ROCKVILLE, Md., June 6, 2024  /PRNewswire/ -- I-Mab (NASDAQ:IMAB) (the "Company"), a U.S.-based, global biotech company, exclusively focused on the development and potential commercialization of highly differentiated immunotherapies for the treatment of cancer, today announced the appointment of Dr. Phillip Dennis as Chief Medical Officer. Dr. Dennis, who will join I-Mab effective June 17, 2024, will lead the Company's global clinical development efforts and serve as a member of I-Mab's Executive Leadership Team. "I am pleased to welcome Dr. Phillip Dennis as our Chief Medical

    6/6/24 7:00:00 AM ET
    $AZN
    $IMAB
    $SNY
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $AZN
    Large Ownership Changes

    This live feed shows all institutional transactions in real time.

    View All

    SEC Form SC 13G/A filed by AstraZeneca PLC (Amendment)

    SC 13G/A - ASTRAZENECA PLC (0000901832) (Subject)

    2/4/22 9:06:48 AM ET
    $AZN
    Biotechnology: Pharmaceutical Preparations
    Health Care

    SEC Form SC 13G/A filed

    SC 13G/A - ASTRAZENECA PLC (0000901832) (Subject)

    2/3/21 1:13:21 PM ET
    $AZN
    Biotechnology: Pharmaceutical Preparations
    Health Care