Natera’s Non-Invasive Prenatal Diagnostic to Detect Down Syndrome, Trisomy 13, Trisomy 18 and Certain Sex Chromosome Abnormalities in the First Trimester of Pregnancy

Posted by: Doctor Medical  :  Category: Health News

REDWOOD CITY, Calif.–(BUSINESS WIRE)–Natera, formerly known as Gene Security Network, today announced that
details about the breadth of the company’s non-invasive prenatal
diagnostic test will be disclosed in presentations during the Society
for Maternal-Fetal Medicine’s 32nd Annual Meeting, February
6-11, in Dallas.

“Non-invasive Prenatal Diagnosis Beyond
Trisomy 21: Using Bioinformatics to Address Low Fetal DNA Fraction in
the First Trimester and Detect Multiple Common Chromosome
Abnormalities”

Natera’s non-invasive prenatal diagnostic test is currently being
evaluated in a clinical trial for detection of multiple disorders,
including Trisomy 21 (Down syndrome), Trisomy 18 (Edwards syndrome),
Trisomy 13 (Patau syndrome) and certain sex chromosome abnormalities.
The diagnostic test, planned for launch later this year, uses fetal DNA
found in a blood sample drawn from the mother within the first trimester
of pregnancy. This is the first clinical trial of a non-invasive
prenatal diagnostic to be funded in part by the National Institutes of
Health (NIH).

“Unlike other non-invasive prenatal diagnostics that test only for Down
Syndrome and Trisomy 18, our test will offer patients and physicians
effective diagnosis of multiple disorders caused by chromosomal
abnormalities,” said Matthew Rabinowitz, Ph.D., chief executive officer
of Natera. “The goal of our non-invasive test is to provide detection
coverage comparable to invasive tests, such as amniocentesis, and
inclusion of these additional abilities will provide disease detection
coverage of more than three times that of other non-invasive tests. We
look forward to continuing to explore these broad uses of our test
through our clinical study, as well as the potential for further
applications in future development.”

Additional details about the test will first be presented during a
satellite symposium, titled “Non-invasive Prenatal Diagnosis Beyond
Trisomy 21: Using Bioinformatics to Address Low Fetal DNA Fraction in
the First Trimester and Detect Multiple Common Chromosome
Abnormalities,” from 6:30 p.m. to 8 p.m. CST on Friday, February 10.

The poster presentations, titled “A novel targeted sequencing approach
improves non-invasive detection of chromosome ploidy on 1st
trimester samples” and “A novel and highly accurate method for
non-invasive prenatal diagnosis using parental genotypes,” will be
delivered from 10 a.m. to noon CST on Saturday, February 11.

About Natera

Natera is a genetic testing company that has developed a proprietary
bioinformatics technology (Parental Support) to deliver accurate and
comprehensive high throughput testing for reproductive indications from
tiny quantities of DNA – as small as that from a single cell. Natera
operates a CLIA laboratory in Redwood City, Calif., providing a host of
preconception and prenatal genetic testing services. Test offerings
include preimplantation genetic diagnosis to analyze chromosomal
anomalies or inherited genetic conditions during an IVF cycle in order
to select embryos with the highest probability of becoming healthy
children; products of conception testing following miscarriage to
rapidly and extensively analyze fetal chromosomes in order to understand
the cause; and non-invasive prenatal testing to determine paternity or
detect genetic disease by analyzing fragments of fetal DNA in a pregnant
mother’s blood drawn in the first trimester. Non-invasive testing for
paternity is currently available worldwide. Natera’s clinical trial for
non-invasive detection of chromosomal anomalies is funded by the NIH and
is being conducted by the leaders in maternal-fetal medicine in the
United States. For more information, visit www.natera.com.

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Medical Properties Trust Announces Public Offering of $200 Million of Senior Notes by Its Operating Partnership and MPT Finance Corporation

Posted by: Doctor Medical  :  Category: Health News

BIRMINGHAM, Ala.–(BUSINESS WIRE)–Medical Properties Trust, Inc. (the “Company”) (NYSE: MPW) announced
today that its operating partnership, MPT Operating Partnership, L.P., a
Delaware limited partnership (the “Operating Partnership”), and MPT
Finance Corporation, a Delaware corporation and wholly owned subsidiary
of the Operating Partnership (“MPT Finance,” and together with the
Operating Partnership, the “Issuers”), are offering $200 million
aggregate principal amount of senior notes due 2022 (the “Notes”). J.P.
Morgan, BofA Merrill Lynch, Deutsche Bank Securities and RBC Capital
Markets will act as joint-book running managers for the proposed
offering. The Notes will be senior unsecured obligations of the Issuers,
guaranteed by the Company and by certain subsidiaries of the Operating
Partnership.

The Operating Partnership intends to use the net proceeds from the
offering of Notes, together with borrowings and net proceeds from other
financing arrangements, to fund the anticipated acquisition of Ernest
Health, Inc. and related transactions (the “Ernest Acquisition
Transactions”), which the Company announced on January 31, 2012, and for
general corporate purposes, including debt repayment and funding future
acquisitions and investments. If the Ernest Acquisition Transactions
have not been consummated on or before the closing of the Notes
offering, the proceeds of the offering will be placed in escrow pending
the completion of the Ernest Acquisition Transactions. If the Ernest
Acquisition Transactions do not close, the Issuer will be required to
redeem the Notes.

The offering of the Notes will be made under the Company’s and Issuers’
shelf registration statement, which became automatically effective upon
filling with the Securities and Exchange Commission (“SEC”). The Company
intends to file a final prospectus with the SEC for the note offering to
which this communication relates. When available, the final prospectus
may be obtained from J.P. Morgan Securities LLC, 383 Madison Avenue, 3rd
Floor, New York, NY 10179, Attn: Syndicate or from Merrill Lynch,
Pierce, Fenner Smith Incorporated, c/o Broadridge Financial Solutions,
1155 Long Island Avenue, Edgewood, NY 11717 or by visiting the EDGAR
database on the SEC’s web site at www.sec.gov.

This press release does not constitute an offer to sell or a
solicitation of an offer to buy the Notes, nor shall there be any sale
of the Notes in any jurisdiction in which such an offer, solicitation or
sale would be unlawful prior to registration or qualification under the
securities laws of any such jurisdiction. The offering may be made only
by means of a prospectus, which has or will be filed with the SEC.

About Medical Properties Trust, Inc.

Medical Properties Trust, Inc. is a Birmingham, Alabama based
self-advised real estate investment trust formed to capitalize on the
changing trends in healthcare delivery by acquiring and developing
net-leased healthcare facilities. These facilities include inpatient
rehabilitation hospitals, long-term acute care hospitals, regional acute
care hospitals, ambulatory surgery centers and other single-discipline
healthcare facilities, such as heart hospitals and orthopedic hospitals.

This press release contains forward-looking statements concerning the
Company’s expectations, anticipations, intentions, beliefs or strategies
regarding the proposed offering of Notes, the use of proceeds from the
offering, and the Ernest Acquisition Transactions. These forward-looking
statements are not promises or guarantees and involve substantial risks
and uncertainties.
Among the factors that could cause actual
results to differ materially from those described or projected herein
are the following: the Issuers’ ability to consummate the offering of
Notes and the use of the proceeds therefrom; the Company’s ability to
obtain or raise additional funds needed to consummate the Ernest
Acquisition Transactions; the Company’s ability to complete the Ernest
Acquisition Transactions on the anticipated time schedule or terms or at
all;
national and economic, business, real estate and other
market conditions; the competitive environment in which the Company
operates; the execution of the Company’s business plan; financing risks;
the Company’s ability to maintain its status as a REIT for federal
income tax purposes; acquisition and development risks; potential
environmental and other liabilities; and other factors affecting the
real estate industry generally or the healthcare real estate in
particular. For further discussion of the factors that could affect
outcomes, please refer to the “A Warning About Forward Looking
Statements” and “Risk Factors” sections of the Company’s Annual Report
Form 10-K for the year ended December 31, 2010, as amended, and as
further updated by the Company’s subsequently filed Quarterly Reports on
Form 10-Q and the Company’s other SEC filings. Except as otherwise
required by law, the Company undertakes no obligation to update the
information in this press release.

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Celerion First Early Stage Contract Research Organization to Adopt a Participant Verification System to Improve Participant Safety and Data Quality

Posted by: Doctor Medical  :  Category: Health News

LINCOLN, Neb.–(BUSINESS WIRE)–Celerion, the premier provider of innovative early stage drug
development solutions, is pleased to announce it has implemented VCT
Verify™ from Verified Clinical Trials, to instantaneously ensure
accurate participant identification and qualification for clinical
research. Celerion is the first Early Stage Contract Research
Organization (CRO) to partner with Verified Clinical Trials to set the
standard for the industry to adopt.

“Celerion continues to apply rigorous standards to protect the safety of
participants and enhance data integrity while supporting our commitment
to our clients. This implementation sets a standard in the industry to
continue to improve clinical research and more effectively bring new
drugs to the market”

Celerion will more effectively screen and select higher quality study
participants by using this tool to instantly identify ineligible
candidates for enrollment. The system searches a global clinical
database registry to identify participants that are currently enrolled
in other clinical studies. Clients benefit from improved participant
selection and higher data integrity.

Celerion chose to implement the VCT Verify™ product across all our
global clinical facilities to solve the long recognized problem of
inaccurate applications that compromise study success. The system has
been reviewed and applauded by numerous Institutional Review Boards
(IRBs) and Verified Clinical Trials is safe harbor certified.

“Celerion continues to apply rigorous standards to protect the safety of
participants and enhance data integrity while supporting our commitment
to our clients. This implementation sets a standard in the industry to
continue to improve clinical research and more effectively bring new
drugs to the market,” said Phil Bach, Vice President of Global Clinical
Research at Celerion. “We are excited to partner with Verified Clinical
Trials, the leader in this specialized field, to take a firm stance on
ensuring the highest quality data and participants for our clients.”

“Verified Clinical Trials offers a comprehensive and unique clinical
research database registry to enhance the quality of both early and late
stage studies globally. The system has been designed to streamline the
clinical trial process and offers protection from various other
potential liabilities,” said Mitchell Efros, MD FACS, CEO at Verified
Clinical Trials. “We are pleased to be working with Celerion, the first
CRO to implement this product, as they continue to demonstrate their
leadership position in the industry.”

About Celerion

Celerion is the premier provider of innovative early stage clinical
research solutions. From facilities strategically located around the
world, advanced scientific and technological expertise is applied to
global clinical research (over 730 beds in Phases 0, I and IIa,
NDA-enabling clinical pharmacology, ADME), clinical pharmacology
sciences, global bioanalytical services (discovery through late stage),
and drug development services. Celerion has a full spectrum of resources
to meet the needs of the pharmaceutical, biotechnology and generic
industries for Phase 0 through IIa proof-of-concept studies. For more
information, visit www.celerion.com.

About Verified Clinical Trials

Verified Clinical Trials is a forward thinking company developed by
experts active in the clinical research community to proactively improve
research subject safety and data quality in clinical research trials.
Verified Clinical Trials defines itself as the world’s leader in the
field of database registries in clinical trial research. Verified
Clinical Trials is the only clinical research database registry designed
specifically to enhance the quality of both early and late phase trials
and has the scalability to reach all sites nationally as well as on a
global level. Verified Clinical Trials offers numerous other value added
services to the clinical research site, CRO, and Pharmaceutical Sponsor,
that prove invaluable with regards to financial and legal issues and
liabilities. For more information, visit www.verifiedclinicaltrials.com.

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New Handheld Narcotics Analyzer Gives Edge to Law Enforcement in War on Drugs

Posted by: Doctor Medical  :  Category: Health News

WALTHAM, Mass.–(BUSINESS WIRE)–Thermo Fisher Scientific Inc., the world leader in serving science,
today introduced Thermo
Scientific TruNarc
, a new handheld narcotics analyzer that gives
local law enforcement a significant technology edge in the war on drugs.
TruNarc® can replace more subjective presumptive
field tests
(color tests) used by law enforcement for decades. The
core technology behind TruNarc – Raman spectroscopy* – effectively puts
a powerful laboratory analyzer in the hands of local law enforcement,
providing more accurate and reliable field testing that expedites
prosecution.

“This technology has the potential to impact the entire system, from the
street to eventual prosecution”

As the frontlines of the war on drugs expand to include new dangers such
as “bath
salts
,” one of many new “designer
drugs” that hit the streets with regularity, advanced law enforcement
technology is needed. Users of TruNarc can not only accurately test
liquid and solid samples for common narcotics such as cocaine,
methamphetamine and MDMA (ecstasy), they will also be able to identify
new threats, such as the synthetic cathinones found in bath salts, as
the reference library in their analyzer can be quickly and easily
updated to include new substances.

A single handheld instrument provides faster, more accurate
identification of multiple narcotics, including future threats; yet it
is easier to use and requires no subjective user interpretation. Law
enforcement can also analyze suspected substances through plastic or
glass, minimizing exposure and preserving evidence integrity.

“This technology has the potential to impact the entire system, from the
street to eventual prosecution,” said Chief Paul Keenan, Quincy Police
Department (Quincy, Mass.). “This easy-to-use instrument could save
valuable time for officers, forensic lab staff and, ultimately,
prosecutors. That’s time – and money – that can be invested back into
the community to ensure we stay steps ahead of a constantly evolving
drug problem.”

TruNarc dramatically reduces the time and expense associated with
drug-related arrests. Once a substance is analyzed, results are
automatically captured for reporting and evidence, streamlining the path
to prosecution and virtually eliminating time-consuming paperwork.
Results are automatically date-stamped and stored for future prosecution.

*Raman spectroscopy is accepted by the Scientific
Working Group for the Analysis of Seized Drugs
as a Category A
analytical technique.

For more information about TruNarc: www.thermoscientific.com/trunarc.

About Thermo Fisher Scientific

Thermo Fisher Scientific Inc. is the world leader in serving science.
Our mission is to enable our customers to make the world healthier,
cleaner and safer. With revenues of nearly $11 billion, we have
approximately 37,000 employees and serve customers within pharmaceutical
and biotech companies, hospitals and clinical diagnostic labs,
universities, research institutions and government agencies, as well as
in environmental and process control industries. We create value for our
key stakeholders through two premier brands, Thermo Scientific and
Fisher Scientific, which offer a unique combination of continuous
technology development and the most convenient purchasing options. Our
products and services help accelerate the pace of scientific discovery,
and solve analytical challenges ranging from complex research to routine
testing to field applications. Visit www.thermofisher.com.

Photos/Multimedia Gallery Available: http://www.businesswire.com/cgi-bin/mmg.cgi?eid=50155210lang=en

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Medical Action Industries Reports Third Quarter 2012 Results

Posted by: Doctor Medical  :  Category: Health News

BRENTWOOD, N.Y.–(BUSINESS WIRE)–Medical Action Industries Inc. (NASDAQ/MDCI), a leading supplier of
medical and surgical disposable products, today reported results for the
fiscal 2012 third quarter ended December 31, 2011.

“We continue to focus on organic growth and enhancing our product and
service offerings”

Net sales for the third quarter of fiscal 2012 were $112,969,000, an
increase of $8,492,000, or 8%, compared to the $104,477,000 in net sales
reported for the comparable prior year period. Net sales for the third
quarter of fiscal 2012 included $34,905,000 in custom procedure tray
sales generated by AVID Medical Inc. (“AVID”), which was acquired by
Medical Action on August 27, 2010. Excluding sales of custom procedure
trays, Medical Action’s net sales for the third quarter of fiscal 2012
were $78,064,000, representing an increase of $6,691,000, or 9%, from
the comparable prior year period.

Net income for the third quarter of fiscal 2012 was $1,825,000 or $0.11
per basic and diluted share, versus the $2,304,000, or $0.14 per basic
and diluted share, reported for the comparable prior year period.

Net sales for the nine months ended December 31, 2011 were $329,097,000,
an increase of $71,876,000 or 28% from the $257,221,000 in net sales
reported for the comparable nine months of fiscal 2011. Net sales for
the nine months ended December 31, 2011 included $102,987,000 in custom
procedure tray sales generated by AVID. Excluding sales of custom
procedure trays, Medical Action’s net sales for the nine months ended
December 31, 2011 were $226,110,000, representing an increase of
$16,131,000 or 8% from the comparable prior year period.

Net income for the nine months ended December 31, 2011 was $2,642,000 or
$0.16 per basic and diluted share, versus the $3,269,000 or $0.20 per
basic and diluted share reported for the comparable prior year period.
Included in net income for the nine months ended December 31, 2011 was
an extraordinary pre-tax gain of $700,000 or $0.03 per basic and diluted
share (net of applicable tax expense) due to an insurance settlement
related to inventories damaged as a result of weather-related flooding.
Net income for the nine months ended December 31, 2010 included an
extraordinary pre-tax loss of $1,455,000 or $0.05 per basic and diluted
share (net of applicable tax benefit) due to inventories damaged as a
result of weather-related flooding and one-time pre-tax transaction
costs of $1,335,000 related to the acquisition of AVID.

“We continue to focus on organic growth and enhancing our product and
service offerings,” said Chief Executive Officer and President, Paul D.
Meringolo. “Net sales have increased from the comparable prior year
period and sequentially. Persistent volatility in raw material costs,
particularly resin and cotton, continue to influence our gross margins.
We are managing through this period of volatility by continually
reviewing our pricing strategies across our product lines, minimizing
product sourcing costs and operating expenses.”

Medical Action invites its shareholders and other interested parties to
attend its conference call at 10 a.m. (ET) on February 1, 2012. You may
participate in the conference call by calling (888) 868-9080 (domestic)
or (973) 935-8511 (international); conference ID #40049844
.
The conference call will be simultaneously web cast on our website: www.medical-action.com.
The complete call and discussion will be available for replay on our
website beginning at 11 a.m. (ET) on February 1, 2012.

Medical Action is a diversified manufacturer and distributor of
disposable medical devices and a leader in many of the markets where it
competes. Its products are marketed primarily to acute care facilities
in domestic and certain international markets. The Company has expanded
its target market to include physician, dental and veterinary offices,
out-patient surgery centers, long-term care facilities and laboratories.
Medical Action’s products are marketed nationally by its direct sales
personnel and extensive network of healthcare distributors. The Company
has preferred vendor agreements with national and regional distributors,
as well as sole and multi-source agreements with group purchasing
organizations. Medical Action’s common stock trades on the NASDAQ Global
Select Market under the symbol MDCI and is included in the Russell 2000
Index.

This news release contains forward-looking statements that involve
risks and uncertainties regarding Medical Action’s operations and future
results.
Please see the Company’s filings with the Securities and
Exchange Commission, including, without limitation, the Company’s Form
10-K and Form 10-Qs, which identify specific factors that would cause
actual results or events to differ materially from those described in
the forward-looking statements.

 

MEDICAL ACTION INDUSTRIES INC.

CONSOLIDATED BALANCE SHEETS

(dollars in thousands, except share and per share data)

 

 

 

 

 

 

 

 

December 31,

March 31,

2011

2011

ASSETS

(Unaudited)

CURRENT ASSETS:

Cash and cash equivalents

 

$

1,003

$

 

1,691

Accounts receivable, less allowance for doubtful accounts of

$818 at December 31, 2011 and $804 at March 31, 2011

35,728

32,330

Inventories, net

55,650

54,674

Prepaid expenses

2,258

1,702

Deferred income taxes

3,008

2,801

Prepaid income taxes

318

1,938

Other current assets

 

1,709

 

 

1,637

Total current assets

99,674

96,773

 

Property, plant and equipment, net

50,205

53,901

Goodwill, net

108,764

108,652

Other intangible assets, net

39,882

41,860

Other assets, net

 

 

2,940

 

 

3,319

Total assets

 

$

301,465

$

304,505

 

LIABILITIES AND STOCKHOLDERS’ EQUITY

CURRENT LIABILITIES:

Accounts payable

 

$

14,272

$

 

17,069

Accrued expenses

22,578

22,235

Current portion of capital lease obligation

121

92

Current portion of long-term debt

 

 

16,000

 

 

16,360

Total current liabilities

52,971

55,756

Deferred income taxes

27,956

27,956

Capital lease obligation, less current portion

13,690

13,790

Long-term debt, less current portion

 

55,470

 

 

58,776

Total liabilities

150,087

156,278

 

STOCKHOLDERS’ EQUITY:

Common stock – 40,000,000 shares authorized, $.001 par value;

issued and outstanding 16,390,628 shares at December 31, 2011 and

16,383,128 shares at March 31, 2011

16

16

Additional paid-in capital

34,308

33,799

Accumulated other comprehensive loss

(437

)

(437

)

Retained earnings

 

117,491

 

 

114,849

Total stockholders’ equity

 

151,378

 

 

148,227

Total liabilities and stockholders’ equity

 

$

301,465

$

 

304,505

 

 

MEDICAL ACTION INDUSTRIES INC.

CONSOLIDATED STATEMENTS OF OPERATIONS

(dollars in thousands, except per share data)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Three Months Ended

December 31,

Nine Months Ended

December 31,

2011

2010

2011

2010

(Unaudited)

(Unaudited)

 

Net sales

$

112,969

$

104,477

$

329,097

$

257,221

Cost of sales

 

95,824

 

86,055

 

278,294

 

211,415

Gross profit

17,145

18,422

50,803

45,806

Selling, general and administrative expenses

 

13,327

 

13,551

 

44,110

 

37,299

Operating income

3,818

4,871

6,693

8,507

Interest expense, net

 

1,174

 

1,116

 

3,421

 

1,742

Income before income taxes and extraordinary item

2,644

3,755

3,272

6,765

Income tax expense

 

819

 

1,451

 

1,070

 

2,600

Income before extraordinary item

1,825

2,304

2,202

4,165

Extraordinary gain (loss), net of applicable taxes

 

-

 

-

 

440

 

(896

)

Net income

$

1,825

$

2,304

$

2,642

$

3,269

 

Per share basis:

Basic

Income before extraordinary item

$

0.11

$

0.14

$

0.13

$

0.25

Extraordinary gain (loss), net of applicable taxes

$

-

$

-

$

0.03

$

(0.05

)

Net income

$

0.11

$

0.14

$

0.16

$

0.20

 

Diluted

Income before extraordinary item

$

0.11

$

0.14

$

0.13

$

0.25

Extraordinary gain (loss), net of applicable taxes

$

-

$

-

$

0.03

$

(0.05

)

Net income

$

0.11

$

0.14

$

0.16

$

0.20

 

 

MEDICAL ACTION INDUSTRIES INC.

CONSOLIDATED STATEMENT OF CHANGES IN STOCKHOLDERS’ EQUITY

NINE MONTHS ENDED DECEMBER 31, 2011

(Unaudited)

(dollars in thousands, except share data)

 

 

 

 

 

 

Common Stock

 

 

 

 

 

 

Additional

Paid-In

Capital

 

 

 

 

 

 

 

 

 

 

Accumulated Other

Comprehensive

Loss

 

 

 

 

 

 

 

 

 

 

Retained

Earnings

 

 

 

 

Total

Stockholders’

Equity

 

Shares

 

 

Amount

 

 

 

 

 

Balance at April 1, 2011

16,383,128

$

 

16

$

33,799

$

(437)

$

114,849

$

148,227

 

Exercise of stock options

7,500

-

20

20

 

Amortization of deferred compensation

15

15

 

Tax benefit from vesting of restricted stock

and exercise of stock options

19

19

 

Stock-based compensation

455

455

 

Net income

2,642

2,642

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Balance at December 31, 2011

 

16,390,628

 

$

 

16

$

34,308

$

(437)

$

117,491

$

151,378

 

 

MEDICAL ACTION INDUSTRIES INC.

CONSOLIDATED STATEMENTS OF CASH FLOWS

(dollars in thousands)

 

 Nine Months Ended December 31,

 

2011

 

 

2010

 

(Unaudited)

CASH FLOWS FROM OPERATING ACTIVITIES:

Net income

 

$

2,642

$

3,269

Adjustments to reconcile net income to net cash used in operating

activities:

Extraordinary (gain) loss

(700

)

1,455

Depreciation

4,394

3,960

Amortization

3,264

2,321

Provision for doubtful accounts

39

9

Deferred income taxes

-

(45

)

Stock-based compensation

470

589

Excess tax liability from stock-based compensation

(207

)

-

Loss on disposal of property and equipment

-

20

Tax benefit from vesting of restricted stock

19

79

and exercise of stock options

Changes in operating assets and liabilities:

Accounts receivable

(3,652

)

303

Inventories

(998

)

(16,372

)

Prepaid expenses and other current assets

72

423

Other assets

(907

)

(1,933

)

Accounts payable

(2,797

)

583

Prepaid income taxes

1,620

8

Accrued expenses

 

343

 

4,955

Net cash provided by (used in) operating activities

 

3,602

 

(376

)

 

CASH FLOWS FROM INVESTING ACTIVITIES:

Purchase price and related acquisition costs

125

(62,525

)

Purchases of property, plant and equipment

(701

)

(2,914

)

Proceeds from sale of property and equipment

 

3

 

4

Net cash used in investing activities

 

(573

)

 

(65,435

)

 

CASH FLOWS FROM FINANCING ACTIVITIES:

Proceeds from revolving line of credit and long-term borrowings

74,217

155,380

Principal payments on revolving line of credit and long-term
borrowings

(77,883

)

(90,428

)

Principal payments on capital lease obligation

(71

)

(20

)

Proceeds from exercise of stock options

 

20

 

152

Net cash (used in) provided by financing activities

 

(3,717

)

 

65,084

 

Net decrease in cash and cash equivalents

(688

)

(727

)

Cash and cash equivalents at beginning of period

 

1,691

 

5,641

Cash and cash equivalents at end of period

 

$

1,003

$

4,914

 

Supplemental disclosures:

Interest paid

 

$

2,347

$

1,189

Income taxes (refunded) paid

 

$

(491

)

$

1,947

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