The Globe and Mail

Go to the Globe and Mail homepage

Jump to main navigationJump to main content

Globe Investor

News Sources

Take control of your investments with the latest investing news and analysis

Press release from GlobeNewswire (a Nasdaq OMX company)

BioMarin Announces Second Quarter 2013 Financial Results

Thursday, July 25, 2013

BioMarin Announces Second Quarter 2013 Financial Results

13:00 EDT Thursday, July 25, 2013

Total Revenue Growth Exceeds 10 Percent

Phase 3 Trial to Start in 3Q 2013

Conference Call and Webcast to be Held Today at 5:00 p.m. ET

Financial Highlights ($ in millions, except per share data, unaudited)
 
Q2 2013

Q2 2012
Percent
Change
Total BioMarin Revenue  $ 136.8  $ 124.0 10.3%
Total BioMarin Revenue (excluding Aldurazyme Net Product Transfer Revenue) - non-GAAP  140.5  120.6 16.5%
Naglazyme Net Product Revenue  69.9  62.9 11.1%
Aldurazyme BioMarin Net Product Revenue   17.5  21.8 -19.7%
Aldurazyme Royalty Revenue (excluding Net Product Transfer Revenue) - non-GAAP  21.2  18.4 15.2%
Kuvan Net Product Revenue  40.9  34.7 17.9%
Firdapse Net Product Revenue  4.1  3.6 13.9%
Net Loss   (21.5)  (32.0)  
Net Loss per Share (basic)  $ (0.15)  $ (0.27)  
Net Loss per Share (diluted)  $ (0.16)  $ (0.27)  
Adjusted EBITDA Loss - non-GAAP  $ 0.0  $ (7.3)  
       
Cash, cash equivalents and short and long-term investments  $ 524.4  $ 524.6 0.0%

SAN RAFAEL, Calif., July 25, 2013 (GLOBE NEWSWIRE) -- BioMarin Pharmaceutical Inc. (Nasdaq:BMRN) today announced financial results for its second quarter ended June 30, 2013. GAAP net loss was $21.5 million ($0.16 per diluted share) for the second quarter of 2013, compared to GAAP net loss of $32.0 million ($0.27 per diluted share) for the second quarter of 2012. GAAP net loss for the six months ended June 30, 2013 was $61.3 million ($0.46 per diluted share), as compared to GAAP net loss of $56.0 million ($0.48 per diluted share) for the six months ended June 30, 2012. Non-GAAP adjusted EBITDA was $0.0 million for the second quarter of 2013, compared to non-GAAP adjusted EBITDA loss of $7.3 million for the second quarter of 2012. Non-GAAP adjusted EBITDA was  a loss of $8.0 million for the six months ended June 30, 2013, as compared to a loss of $7.2 million for the six months ended June 30, 2012. The decreased GAAP net loss and the decreased non-GAAP adjusted EBITDA loss for the second quarter of 2013 compared to the second quarter of 2012 was primarily due to higher total revenue and a smaller increase in operating expenses.

As of June 30, 2013, BioMarin had cash, cash equivalents and short and long-term investments totaling $ 524.4 million, as compared to $525.7 million on March 31, 2013. 

"In the second quarter, we continued to execute on our development goals as we head into the second half of the year," said Jean-Jacques Bienaimé, Chief Executive Officer of BioMarin. "We made good progress in a number of important areas including commercial, R&D and regulatory. Highlights included initiation of the Phase 3 PEG-PAL trial for PKU, confirmation of priority review status for Vimizim in the U.S., validation of the MAA by the EMA, submission of the Vimizim MA in Brazil and a positive update of the ongoing BMN 673 trial for genetically-defined cancers at the ASCO annual meeting. We are pleased with the momentum of the BMN 673 program because of maturing and improving responses, completed positive regulatory discussions and earlier Phase 3 timelines than originally anticipated. We remain on track to meet our upcoming goals for the remainder of the year."

Net Product Revenue (in millions)                 
                 
  Three Months Ended June 30, Six Months Ended June 30,
  2013 2012 $ Change % Change 2013 2012 $ Change % Change
                 
Naglazyme (1)  $ 69.9  $ 62.9  $ 7.0 11.1%  $ 139.3  $ 131.5  $ 7.8 5.9%
Kuvan  40.9  34.7  6.2 17.9%  78.5  66.7  11.8 17.7%
Firdapse  4.1  3.6  0.5 13.9%  7.7  7.2  0.5 6.9%
Aldurazyme  17.5  21.8  (4.3) -19.7%  34.2  33.8  0.4 1.2%
Net Product Revenues  132.4  123.0  9.4 7.6%  259.7  239.2  20.5 8.6%
                 
Collaborative agreement revenues  0.9  0.4  0.5    1.0  0.6  0.4  
Royalty and license revenue  3.5  0.6  2.9    4.0  0.9  3.1  
Total BioMarin Revenues - GAAP  136.8  124.0  12.8 10.3%  264.7  240.7  24.0 10.0%
                 
Less: Aldurazyme Net Product Transfer Revenues   (3.7)  3.4  (7.1)    (6.3)  (3.0)  (3.3)  
Total BioMarin Revenues (excluding Aldurazyme                 
Net Product Transfer Revenue) - non-GAAP (2)    $ 140.5  $ 120.6  $ 19.9 16.5%  $ 271.0  $ 243.7  $ 27.3 11.2%
                 
Reconciliation of Aldurazyme Revenue (in millions)
                 
  Three Months Ended June 30,  Six Months Ended June 30, 
  2013 2012 $ Change % Change  2013 2012 $ Change % Change 
Aldurazyme revenue reported by Genzyme  $53.6  $45.8  $7.8 17.0%  $102.1  $91.7 $ 10.4 11.3%
                 
                 
Aldurazyme Royalties due from Genzyme - Non-GAAP (2)  21.2  18.4  2.8    40.5  36.8  3.7  
Incremental product transfer revenues (3)  (3.7)  3.4  (7.1)    (6.3)  (3.0)  (3.3)  
Total Aldurazyme net product revenues - GAAP $17.5  $21.8  $(4.3)    $34.2  $33.8  $0.4  
                 
(1)  Naglazyme revenues experience quarterly fluctuations due to the timing of government ordering patterns in certain countries.
 
(2)  BioMarin believes that this non-GAAP information is useful to investors, taken in conjunction with BioMarin's GAAP information because it provides additional information regarding the performance of BioMarin's core business. By providing information about both the GAAP and non-GAAP revenue measures, the company believes that the additional information enhances investors' overall understanding of the company's business and in particular allows for more consistent period to period evaluation of the revenue.
 
(3)  To the extent units shipped to third party customers by Genzyme exceed BioMarin inventory transfers to Genzyme, BioMarin will record a decrease in net product revenue from the royalty payable to BioMarin for the amount of previously recognized product transfer revenue. If BioMarin inventory transfers exceed units shipped to third party customers by Genzyme, BioMarin will record incremental net product transfer revenue for the period. 
     
2013 Full Year Financial Guidance    
     
Revenue Guidance ($ in millions)    
Item 2013 Guidance Previous 2013 Guidance
Total BioMarin Revenues $530 to $555 Unchanged
Naglazyme Net Product Revenue $265 to $285 Unchanged
Kuvan Net Product Revenue $155 to $170 Unchanged
     
Selected Income Statement Guidance ($ in millions)    
Item 2013 Guidance Previous 2013 Guidance
Cost of Sales (% of Total Revenue) 17% to 18% Unchanged
Selling, General and Admin. Expense $220 to $240 $220 to $250
Research and Development Expense $340 to $380 Unchanged
GAAP Net Loss $(185) to $(160) $(195) to $(170)
Non-GAAP Adjusted EBITDA (loss) $(65) to $(40) $(75) to $(50)
     
Cash Balance* Over $440 Over $420
     
* Cash balance includes cash, cash equivalents and short and long term investments
 
Anticipated Upcoming Milestones 
 
3Q 2013: Initiation of Phase 1/2 trial for BMN 190 for Batten disease
3Q 2013: Initiation of Phase 3 trial for BMN 673 for BRCA breast cancer
4Q 2013: Initiation of Phase 2/3 switching trial for BMN 701 for Pompe disease
4Q 2013: Potential CHMP opinion for Vimizim for MPA IVA
4Q 2013/1Q 2014: Initiation of Phase 1/2 trial for BMN 111 for achondroplasia
1Q 2014: PDUFA date for Vimizim for MPS IVA
1Q 2014: Potential launch of Vimizim for MPS IVA
4Q 2014: Top-line results for Phase 3 trial for PEG-PAL for PKU

Research and Development Programs

BioMarin continues to make significant progress in research and development to ensure a strong pipeline for the company. The current pipeline includes programs in various stages of development that focus on treating a range of rare and serious unmet medical needs.     

Programs Under Regulatory Review for Approval

  • Vimizim for MPS IVA: During the second quarter, regulatory advancements were made worldwide. The FDA granted Vimizim priority review designation and assigned a PDUFA date of February 28, 2014. The EMA has validated the Vimizim MAA and has granted accelerated review status, which could lead to a CHMP opinion before year end. During the second quarter, the company also submitted the MA in Brazil. Ongoing production of bulk drug substance and drug product will allow for a global launch following approvals in multiple countries. Both the FDA and EMA have conducted or scheduled pre-approval inspections associated with the review of the marketing applications.

Advanced Clinical Programs

  • PEG-PAL for PKU: The company initiated a pivotal Phase 3 study in the second quarter of 2013. The Phase 3 program includes (1) an open-label study to evaluate safety and blood Phe levels in naïve patients and (2) a randomized controlled study of the Phase 2 extension study patients and patients from the open label trial to evaluate blood Phe levels and neurocognitive endpoints, which is expected to be initiated in the third quarter of 2013. The company expects top-line results for the Phase 3 study in the fourth quarter of 2014.
     
  • BMN 701 for Pompe Disease: The company plans to initiate a Phase 2/3 switching trial by the end of 2013 in late-onset Pompe patients who have previously been treated with alglucosidase alfa. Subject to discussions with health authorities, the proposed study design is a single arm trial, with treatment at 20 mg/kg administered every other week for 24 weeks and the respiratory parameter MIP as the primary endpoint. The company has completed a full scale production campaign using its new higher producing cell line and has verified the production yields. Characterization testing is currently ongoing, and it is expected that regulatory filings to support the introduction of this material into clinical studies will be submitted in the fourth quarter of 2013.
     
  • BMN 673 (PARP inhibitor): As of July 24, the RECIST response rate from the ongoing trial is nine out of 18 breast cancer patients, or 50 percent, including one confirmed complete response. This response rate includes three additional confirmed responses since the last update at the ASCO Annual Meeting, and two new patients are yet to be confirmed. Four patients are ongoing with stable disease with potential for additional responses. All patients have been on treatment for at least twelve weeks. The study is still ongoing, and the company will provide additional updates later this year, including data in ovarian cancer, Ewing's sarcoma and small cell lung cancer. BioMarin now expects to initiate a Phase 3 trial for BMN 673 in deleterious gBRCA mutation metastatic breast cancer in late third quarter of 2013, earlier than previously announced at the ASCO Annual Meeting in early June.  

Early-Stage Clinical Programs

  • BMN 111 for Achondroplasia: The company is modifying its clinical program based on a request from the Food and Drug Administration (FDA) for more clinical pharmacokinetic and safety data in children with the disease. BioMarin previously completed a Phase 1 study in adult healthy volunteers. Although the FDA acknowledges that the company has identified a range of doses that are relatively well-tolerated short–term, it has now requested additional PK and safety data in children with achondroplasia before proceeding to extended dosing in children. The FDA has placed the BMN 111 program on partial clinical hold. The company will work with the appropriate health authorities on the implications on the program. The company expects to initiate its first study in pediatric patients in the fourth quarter of 2013 or the first quarter of 2014.
     
  • BMN 190 for LINCL (Batten disease): BioMarin filed a CTA in the first quarter of 2013 and expects to begin enrolling the study in the third quarter of 2013. 

Preclinical Programs

  • Other early stage programs: BioMarin is working on multiple additional early development opportunities, including two new lead optimization programs gained through the acquisition of Zacharon Pharmaceuticals: inhibition of heparan sulfate synthesis for MPS III and inhibition of ganglioside synthesis for diseases such as Tay Sachs and Sandhoff. The company also has an ongoing Factor VIII gene therapy research program for Hemophilia A from University College London and St. Jude Children's Research Hospital.

Non-GAAP Adjusted EBITDA Reconciliation

The results for the three and six months ended June 30, 2013 and June 30, 2012 and financial guidance for the year ending December 31, 2013 are all determined in accordance with GAAP except for non-GAAP adjusted EBITDA which is determined on a non-GAAP basis. As used in this release, non-GAAP adjusted EBITDA is based on GAAP earnings before interest, taxes, depreciation and amortization (EBITDA) and further adjusted to also exclude certain non-cash stock compensation expense, non-cash contingent consideration expense and certain other nonrecurring material items (non-GAAP adjusted EBITDA). 

The following table presents the reconciliation of non-GAAP to GAAP financial metrics:

Reconciliation of GAAP Net Loss to Non-GAAP Adjusted EBITDA Loss
(in millions)
(unaudited) 
 
    Three Months Ended
June 30, 
Six Months Ended
June 30, 
Year Ending
December 31, 
  NOTES 2013 2012 2013 2012 2013 Guidance
             
GAAP Net Loss    $ (21.5)  $ (32.0)  $ (61.3)  $ (56.0)  $(185.0) - $(160.0) 
             
Interest expense, net    --   1.4  1.0  2.8  0.7 
Provision for (benefit from) income taxes     1.2  (0.4)  (3.5)  (0.4)  (14.6) 
Depreciation expense    6.6  7.2  12.7  14.5  27.0 
Amortization expense    3.6  2.7  6.2  12.0  11.5 
EBITDA Loss    (10.1)  (21.1)  (44.9)  (27.1)  (160.4) - (135.4) 
             
Stock-based compensation expense    13.9  12.6  25.5  23.8  70.0 
Contingent consideration expense (1)   (3.8)  1.2  1.0  (3.9)  15.0 
Material non-recurring:            
Debt conversion expense (2)  --   --   10.4  --   10.4 
             
Non-GAAP Adjusted EBITDA Loss    $ 0.0  $ (7.3)  $ (8.0)  $ (7.2)  $(65.0) - $(40.0) 
           
(1) Represents the expense associated with the change in the fair value of contingent acquisition consideration payable for the period. The change in the current quarter reflects changes in estimated probabilities and timing of achieving certain developmental milestones.
 
(2) Represents debt conversion expense associated with the early conversion of a portion of our 2017 convertible notes in March 2013.

BioMarin believes that this non-GAAP information is useful to investors, taken in conjunction with BioMarin's GAAP information because it provides additional information regarding the performance of BioMarin's core ongoing business, Naglazyme, Kuvan, Aldurazyme and Firdapse and development of its pipeline. By providing information about both the overall GAAP financial performance and the non-GAAP measures that focus on continuing operations, the company believes that the additional information enhances investors' overall understanding of the company's business and prospects for the future. Further, the company uses both the GAAP and the non-GAAP results and expectations internally for its operating, budgeting and financial planning purposes.

Conference Call Details

BioMarin will host a conference call and webcast to discuss second quarter 2013 financial results today, Thursday, July 25, 2013 at 5:00 p.m. ET. This event can be accessed on the investor section of the BioMarin website at www.BMRN.com.

Date: July 25, 2013
Time: 5:00 p.m. ET
U.S. / Canada Dial-in Number: 877.303.6313
International Dial-in Number: 631.813.4734
Conference ID: 13894023
 
Replay Dial-in Number: 855.859.2056
Replay International Dial-in Number: 404.537.3406
Conference ID: 13894023

About BioMarin

BioMarin develops and commercializes innovative biopharmaceuticals for serious diseases and medical conditions. The company's product portfolio comprises four approved products and multiple clinical and pre-clinical product candidates. Approved products include Naglazyme® (galsulfase) for mucopolysaccharidosis VI (MPS VI), a product wholly developed and commercialized by BioMarin; Aldurazyme® (laronidase) for mucopolysaccharidosis I (MPS I), a product which BioMarin developed through a 50/50 joint venture with Genzyme Corporation; Kuvan® (sapropterin dihydrochloride) Tablets, for phenylketonuria (PKU), developed in partnership with Merck Serono, a division of Merck KGaA of Darmstadt, Germany; and Firdapse® (amifampridine), which has been approved by the European Commission for the treatment of Lambert Eaton Myasthenic Syndrome (LEMS). Product candidates include Vimizim (N-acetylgalactosamine 6-sulfatase), formally referred to as GALNS, which successfully completed Phase III clinical development for the treatment of MPS IVA, PEG-PAL (PEGylated recombinant phenylalanine ammonia lyase), which is currently in Phase III clinical development for the treatment of PKU, BMN-701, a novel fusion protein of insulin-like growth factor 2 and acid alpha glucosidase (IGF2-GAA), which is currently in Phase I/II clinical development for the treatment of Pompe disease, BMN-673, a poly ADP-ribose polymerase (PARP) inhibitor, which is currently in Phase I/II clinical development for the treatment of genetically-defined cancers, and BMN-111, a modified C-natriuretic peptide, which is currently in Phase I clinical development for the treatment of achondroplasia. For additional information, please visit www.BMRN.com. Information on BioMarin's website is not incorporated by reference into this press release.

Forward-Looking Statement

This press release contains forward-looking statements about the business prospects of BioMarin Pharmaceutical Inc., including, without limitation, statements about: the expectations of revenue and sales related to Naglazyme, Kuvan, Firdapse, and Aldurazyme; the financial performance of the BioMarin as a whole; our expectations regarding the progress and timing of BioMarin's clinical trials of PEG-PAL, BMN-673, BMN-701, BMN-111 and other product candidates; the continued clinical development and commercialization of Aldurazyme, Naglazyme, Kuvan, Firdapse, and its product candidates; our expectations regarding the timing of our regulatory filings for Vimizim and our other product candidates; and actions by regulatory authorities, particularly actions related to Vimizim. These forward-looking statements are predictions and involve risks and uncertainties such that actual results may differ materially from these statements. These risks and uncertainties include, among others: our success in the continued commercialization of Naglazyme, Kuvan, and Firdapse; Genzyme Corporation's success in continuing the commercialization of Aldurazyme; results and timing of current and planned preclinical studies and clinical trials, particularly with respect to PEG-PAL, BMN-673, BMN-701 and BMN-111; our ability to successfully manufacture our products and product candidates; the content and timing of decisions by the U.S. Food and Drug Administration, the European Commission and other regulatory authorities concerning Vimizim and each of the other described products and product candidates; the market for each of these products and particularly Aldurazyme, Naglazyme, Kuvan and Firdapse; actual sales of Aldurazyme, Naglazyme Kuvan and Firdapse; Merck Serono's activities related to Kuvan; and those risks that are discussed  in BioMarin's filings with the Securities and Exchange Commission, including, without limitation, BioMarin's 2012 Annual Report on Form 10-K, and our periodic reports on Form 10-Q and Form 8-K. Stockholders are urged not to place undue reliance on forward-looking statements, which speak only as of the date hereof. BioMarin is under no obligation, and expressly disclaims any obligation to update or alter any forward-looking statement, whether as a result of new information, future events or otherwise.

Vimizim™ is our trademark, and BioMarin®, Naglazyme®, Kuvan®, Firdapse® are registered trademarks of BioMarin Pharmaceutical Inc.

Aldurazyme® is a registered trademark of BioMarin/Genzyme LLC.

BIOMARIN PHARMACEUTICAL INC.
     
CONDENSED CONSOLIDATED BALANCE SHEETS
June 30, 2013 and December 31, 2012
(In thousands of U.S. dollars, except share and per share amounts)
     
     
  June 30, 2013 December 31, 2012(1) 
ASSETS  (unaudited)  
Current assets:    
Cash and cash equivalents  $175,445  $180,527
Short-term investments  225,116  270,211
Accounts receivable, net (allowance for doubtful accounts: $376 and $348, respectively)  115,063  109,066
Inventory  142,296  128,695
Current deferred tax assets  29,474  29,454
Other current assets  33,526  25,509
 Total current assets  720,920  743,462
Noncurrent assets:    
Investment in BioMarin/Genzyme LLC  1,001  1,080
Long-term investments  123,905  115,993
Property, plant and equipment, net  282,002  284,473
Intangible assets, net  168,434  162,980
Goodwill  54,975  51,543
Long-term deferred tax assets  235,400  225,501
Other assets  14,883  16,611
 Total assets  $1,601,520  $1,601,643
LIABILITIES AND STOCKHOLDERS' EQUITY    
Current liabilities:    
Accounts payable and accrued liabilities  $142,241  $147,068
Convertible debt  --   23,365
Total current liabilities  142,241  170,433
Noncurrent liabilities:    
Long-term convertible debt  109,822  324,859
Long-term contingent acquisition consideration payable  23,261  30,618
Long-term deferred tax liabilities  37,182  33,296
Other long-term liabilities  30,756  26,674
Total liabilities  343,262  585,880
Stockholders' equity:    
Common stock, $0.001 par value: 250,000,000 shares authorized at June 30, 2013 and December 31, 2012; 140,050,009 and 125,809,162 shares issued and outstanding at June 30, 2013 and December 31, 2012, respectively.  140  126
Additional paid-in capital  1,863,961  1,561,890
Company common stock held by Nonqualified Deferred Compensation Plan  (7,493)  (6,603)
Accumulated other comprehensive income (loss)  2,441  (202)
Accumulated deficit  (600,791)  (539,448)
Total stockholders' equity  1,258,258  1,015,763
Total liabilities and stockholders' equity  $1,601,520  $1,601,643
     
(1) December 31, 2012 balances were derived from the audited consolidated financial statements.
 
BIOMARIN PHARMACEUTICAL INC.
 
CONDENSED CONSOLIDATED STATEMENTS OF COMPREHENSIVE LOSS
Three and Six Months Ended June 30, 2013 and 2012
(In thousands of U.S. dollars, except per share amounts)
(Unaudited) 
         
  Three Months Ended
June 30,
Six Months Ended
June 30, 
  2013 2012 2013 2012
REVENUES:        
Net product revenues  $132,400  $122,991  $259,744  $239,230
Collaborative agreement revenues  889  423  1,024  519
Royalty and license revenues  3,521  605  3,970  919
Total revenues  136,810  124,019  264,738  240,668
OPERATING EXPENSES:        
Cost of sales (excludes amortization of certain acquired intangible assets)  22,567  23,574  43,067  40,679
Research and development  85,661  77,812  169,404  151,646
Selling, general and administrative  50,656  51,539  101,706  96,787
Intangible asset amortization and contingent consideration  (2,022)  2,048  3,534  4,376
Total operating expenses  156,862  154,973  317,711  293,488
LOSS FROM OPERATIONS  (20,052)  (30,954)  (52,973)  (52,820)
Equity in the income (loss) of BioMarin/Genzyme LLC  (163)  102  (564)  (632)
Interest income  650  536  1,368  1,041
Interest expense  (603)  (1,925)  (2,328)  (3,872)
Debt conversion expense  --   --   (10,420)  -- 
Other income (expense)  (123)  (176)  105  (140)
LOSS BEFORE INCOME TAXES  (20,291)  (32,417)  (64,812)  (56,423)
Provision for (benefit from) income taxes  1,242  (411)  (3,469)  (445)
NET LOSS  $(21,533)  $(32,006) $(61,343)  $(55,978)
NET LOSS PER SHARE, BASIC  $(0.15)  $(0.27) $(0.46)  $(0.48)
NET LOSS PER SHARE, DILUTED  $(0.16)  $(0.27)  $(0.46)  $(0.48)
         
Weighted average common shares outstanding, basic  139,400 117,912 133,716 116,496
Weighted average common shares outstanding, diluted 139,596 117,912 133,716 116,496
         
COMPREHENSIVE LOSS   $(20,247)  $(29,868)  $(58,700)  $(56,215)
 
STOCK-BASED COMPENSATION EXPENSE
         
Total stock-based compensation expense included in the Condensed Consolidated Statements of Comprehensive Loss is as follows:
         
  Three Months Ended Six Months Ended
  June 30,  June 30,
  2013 2012 2013 2012
  (unaudited) (unaudited) (unaudited) (unaudited)
Cost of sales $1,130 $1,335 $2,174 $2,207
Research and development 6,381 5,468 11,705 10,290
Selling, general and administrative 6,418 5,834 11,615 11,268
  $13,929 $12,637 $25,494 $23,765
CONTACT: Investors and Media:
Debra Charlesworth
BioMarin Pharmaceutical Inc.
(415) 455-7451

BioMarin Pharmaceutical Inc. Logo

Products
  • Globe Unlimited

    Digital all access pass across devices. subscribe

  • The Globe and Mail Newspaper

    Newspaper delivered to your doorstep. subscribe

  • Globe2Go

    The digital replica of our newspaper. subscribe

  • Globe eBooks

    A collection of articles by the Globe. subscribe

See all Globe Products

Advertise with us

GlobeLink.ca

Your number one partner for reaching Canada's Influential Achievers. learn more

The Globe at your Workplace
Our Company
Customer Service
Globe Recognition
Mobile Apps
NEWS APP
INVESTING APP
Other Sections