Monthly Archives: September 2017

Pharma-Bio Serv, Inc. Provides Operational Update Following Hurricane Maria

DORADO, PUERTO RICO / ACCESSWIRE / September 28, 2017 / Pharma-Bio Serv, Inc. (“Pharma-Bio Serv” or the “Company”) (OTCQB: PBSV), a compliance, project management, and technology transfer support consulting firm that provides services to the pharmaceutical, biotechnology, chemical, medical device, cosmetic, food, and allied products industries, today announced an update regarding operations following Hurricane Maria.

First and foremost, our personnel have been safely accounted for and many have returned to work in our Dorado office as we work towards resuming normal operations.

Pharma-Bio Serv’s corporate offices, assets, and laboratory in Puerto Rico appear to have not suffered any structural damage during Hurricane Maria and the Company expects minimal cleanup and recovery costs. Our laboratory is running on our diesel dependent generator, which was designed to support our lab systems and personnel. Resources are being acquired to provide additional backup capabilities and we are evaluating additional alternatives for power supply and access to diesel, which are the primary challenges for all Puerto Rico businesses during this recovery. We are also utilizing our recovery location in San Juan to quickly respond in the aftermath of the hurricane. In addition, our US, Spain, Ireland and South American divisions are fully operational and are providing assistance to the workforce in Puerto Rico. We are also evaluating the use of remote facilities in the US.

Most of our customers in Puerto Rico have been contacted and are in various stages of recovery. Although we likely will continue to feel the effects of the hurricane for the next few months, we believe we will begin placing some of our resources in customer locations as early as next week.

While Puerto Rico has clearly suffered tremendously from Hurricane Maria and much of the island’s infrastructure and communication networks are still greatly impaired, we will continue working aggressively on your behalf.

About Pharma-Bio Serv, Inc.

Pharma-Bio Serv is a compliance, project management, and technology transfer support consulting firm, headquartered in Puerto Rico, with operations in the U.S., Ireland, and Spain. Pharma-Bio Serv’s core business is FDA and other international regulatory compliance agency related services, with integrated portfolio services including microbiological and chemical testing services for clients in the Pharmaceutical, Biotechnology, Chemical, Medical Device, Cosmetic, Food and Allied Products industries. The Company’s services also include “Pharma Serv Academy,” a division that provides technical and regulatory standards seminars/training conducted by industry experts. The Company’s global team includes leading engineering and life science professionals, quality assurance managers and directors.

Forward-Looking Statements

This news release contains “forward-looking statements” within the meaning of the U.S. federal securities laws, which statements may include information regarding the plans, intentions, expectations, future financial performance, or future operating performance of Pharma-Bio Serv. Forward-looking statements are based on the expectations, estimates, or projections of management as of the date of this news release. Although Pharma-Bio Serv’s management believes these expectations, estimates, or projections to be reasonable as of the date of this news release, forward-looking statements are inherently subject to significant business risks, economic and competitive uncertainties, or other contingencies, which could cause its actual results or performance to differ materially from what may be expressed or implied in the forward-looking statements. Important factors that could cause Pharma-Bio Serv’s actual results or performance to differ materially from the forward-looking statements include those set forth in the “Risk Factors” section of Pharma-Bio Serv’s Annual Report on Form 10-K for the year ended October 31, 2016, and in its other filings with the Securities and Exchange Commission, which filings are available on www.sec.gov. Pharma-Bio Serv disclaims any intention or obligation to update or revise any forward-looking statements to reflect subsequent events and circumstances, except to the extent required by applicable law.

Company Contact:

Pedro J. Lasanta
Chief Financial Officer
787 278 2709

SOURCE: Pharma-Bio Serv, Inc.

ReleaseID: 476624

Stable Isotope-Labeled Compounds Market worth 294.2 Million USD by 2022

The stable isotope-labeled compounds market is expected to reach USD 294.2 Million by 2022 from an estimated USD 254.6 Million in 2017, at a CAGR of 2.94%.

Seattle, The United States – September 28, 2017 /MarketersMedia/

Browse 66 Market Data Tables and 29 Figures spread through 133 Pages and in-depth TOC on “Stable Isotope Labelled Compounds Market by Type (C13, D, 018, N15 label), Application (Research, Clinical Diagnostics, Industrial), End User (Pharmaceutical and Biotechnology Companies, Academic and Research Institutes, Hospital) – Global Forecast to 2022”
http://www.marketsandmarkets.com/Market-Reports/stable-isotope-labeling-market-53034199.html
Early buyers will receive 10% customization on reports.

The key factors driving the growth of this market include rising proteomics research, increasing research activities in the pharmaceutical and biotechnology sector, and rising prevalence of cancer. However, the high cost of stable isotope-labeled compounds may hinder the growth of this market to a certain extent.

By type, the Deuterium (H-2) segment to account for the largest share of the market in 2017

On the basis of type, the stable-isotope-labelling market is broadly segmented into Carbon-13, Deuterium (H-2), Oxygen-18, Nitrogen-15, and others (noble gases and metals). In 2017, Deuterium (H-2) is expected to account for the largest share of this market and projected to grow at the highest CAGR during the forecast period. This is primarily attributed to increasing use of H-2 in several research and industrial applications.

By application, the research segment to hold the largest market share in 2017

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Based on the application of stable isotope-labeled compounds, the market is further classified into research, clinical diagnostics, industrial, and other applications. In 2017, the research segment is expected to account for the largest share of the stable isotope-labeled compounds market and is expected to grow at the highest CAGR during the forecast period.

The highest growth of this segment is mainly attributed to increasing research activities and funding in areas of biomedical, pharmaceutical, environmental & ecological, and agricultural research.

By end user, the pharmaceutical & biotechnology companies segment to account for the largest market share in 2017

Based on end user, the stable-isotope-labelling market is segmented into pharmaceutical and biotechnology companies, hospitals and diagnostic centers, academic & research institutes, and other end users (contract research organizations, food & beverage companies, and forensic laboratories). In 2017, the pharmaceutical and biotechnology companies segment is expected to account for the largest share of the market. Increased use of stable isotope-labeled compounds in R&D in the pharmaceutical and biotechnology sector is one of the major factors driving the growth of this segment.

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North America to dominate the market in 2017

In 2017, North America is expected to account for the largest share of the stable isotope-labeled compounds market, followed by Europe. Factors such as growth of the pharmaceutical and biopharmaceutical industry, support for this sector from the Isotope Production and Distribution Program Fund, the presence of a large nuclear industry in the U.S., growth of the Canadian pharmaceutical industry, and the rising adoption of PET imaging in Canada are contributing to the large share of the North American region.

Increasing pharmaceutical R&D and the presence of a large number of research institutes & CROs in Germany, increasing number of PET-CT procedures and favourable scenario for environmental research in the U.K., rising metabolomics research in France, and the increase in R&D expenditure in the pharmaceutical industry in the RoE are majorly contributing to the growth of the European stable isotope-labeled compounds market, which holds the second-largest market share.

The key players in the global stable isotope-labeled compounds market include Cambridge Isotopes Laboratories, Inc. (U.S.), Merck KGaA (Germany), URENCO (U.K.), IsoSciences, LLC (U.S.), Medical Isotopes, Inc. (U.S.), Omicron Biochemicals, Inc. (U.S.), Nordion (Canada) Inc., Trace Sciences International (U.S.), Alsachim (France), Taiyo Nippon Sanso Corporation (Japan), PerkinElmer Inc. (U.S.), and Rotem Industries Israel, Ltd. (Israel).

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Source URL: https://marketersmedia.com/stable-isotope-labeled-compounds-market-worth-294-2-million-usd-by-2022/244052

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Source: MarketersMedia

Release ID: 244052

Global Testosterone Replacement Therapy Market Overview and Scope 2017 to 2022

The research study focuses on Global Testosterone Replacement Therapy Market major leading industry players with information such as company profiles, product picture and specification, capacity, production, price, cost, revenue and contact information.

September 28, 2017 /MarketersMedia/

Global Testosterone Replacement Therapy Market Professional Survey Report 2017 presents an in-depth assessment of the Testosterone Replacement Therapy including enabling technologies, key trends, market drivers, challenges, standardization, regulatory landscape, deployment models, operator case studies, opportunities, future roadmap, value chain, ecosystem player profiles and strategies. The report also presents forecasts for Testosterone Replacement Therapy investments from 2017 till 2022.

This study answers several questions for stakeholders, primarily which market segments they should focus upon during the next five years to prioritize their efforts and investments. These stakeholders include Testosterone Replacement Therapy manufacturers such as AbbVie, Endo International, Eli lilly, Pfizer, Actavis (Allergan), Bayer, Novartis, Teva, Mylan, Upsher-Smith, Ferring Pharmaceuticals, Kyowa Kirin and Acerus Pharmaceuticals.

This report segments the global Testosterone Replacement Therapy market on the basis of types, Gels, Injections, Patches and Other. On the basis of application, the global Testosterone Replacement Therapy market is segmented into Hospitals, Clinics and Others.

Order a copy of this research at https://www.marketinsightsreports.com/report/purchase/09271168?mode=su

Primary sources are mainly industry experts from core and related industries, and suppliers, manufacturers, distributors, service providers, and organizations related to all segments of the industry’s supply chain. The bottom-up approach was used to estimate the global market size of Testosterone Replacement Therapy based on end-use industry and region, in terms of value. With the data triangulation procedure and validation of data through primary interviews, the exact values of the overall parent market, and individual market sizes were determined and confirmed in this study.

Geographically, this report is segmented into several key Regions, with production, consumption, revenue (million USD), and market share and growth rate of Testosterone Replacement Therapy in these regions, from 2012 to 2022 (forecast), covering North America (USA, Canada and Mexico), Europe (Germany, France, UK, Russia and Italy), Asia-Pacific (China, Japan, Korea, India and Southeast Asia), South America (Brazil, Argentina, Columbia etc.) and Middle East and Africa (Saudi Arabia, UAE, Egypt, Nigeria and South Africa).

Browse Full Report at: https://www.marketinsightsreports.com/reports/09271168/global-testosterone-replacement-therapy-market-research-report-2017

The research provides answers to the following key questions:

• What will be the market size and the growth rate in 2022?
• What are the key factors driving the global Testosterone Replacement Therapy market?
• Who are the key market players and what are their strategies in the global Testosterone Replacement Therapymarket?
• Trending factors influencing the market shares of the North America, Europe, China, Japan, and Southeast Asia, India.
• What are the key market trends impacting the growth of the global Testosterone Replacement Therapy market?
• What trends, challenges and barriers are influencing its growth?
• What are the market opportunities and threats faced by the vendors in the global Testosterone Replacement Therapy market?
• What are the key outcomes of the five forces analysis of the global Testosterone Replacement Therapy market?

This independent 157 pages report guarantees you will remain better informed than your competition. With over 170 tables and figures examining the Testosterone Replacement Therapy market, the report gives you a visual, one-stop breakdown of the leading products, submarkets and market leader’s market revenue forecasts as well as analysis to 2022.

There are 15 Chapters to deeply display the global Testosterone Replacement Therapy market.

Chapter 1, to describe Testosterone Replacement Therapy Introduction, product scope, market overview, market opportunities, market risk, market driving force;

Chapter 2, to analyze the top manufacturers of Grain and Seed Cleaning Equipment, with sales, revenue, and price of Grain and Seed Cleaning Equipment, in 2016 and 2017;

Chapter 3, to display the competitive situation among the top manufacturers, with sales, revenue and market share in 2016 and 2017;

Chapter 4, to show the global market by regions, with sales, revenue and market share of Grain and Seed Cleaning Equipment, for each region, from 2012 to 2017;

Chapter 5, 6, 7,8and 9, to analyze the key regions, with sales, revenue and market share by key countries in these regions;
Chapter 10and 11, to show the market by type and application, with sales market share and growth rate by type, application, from 2012 to 2017;

Chapter 12, Testosterone Replacement Therapy market forecast, by regions, type and application, with sales and revenue, from 2017 to 2022;

Chapter 13, 14 and 15, to describe Testosterone Replacement Therapy sales channel, distributors, traders, dealers, Research Findings and Conclusion, appendix and data source.

The report provides a basic overview of the Testosterone Replacement Therapy industry including definitions, classifications, applications and industry chain structure. And development policies and plans are discussed as well as manufacturing processes and cost structures.

Then, the report focuses on global major leading industry players with information such as company profiles, product picture and specifications, sales, market share and contact information. What’s more, the Testosterone Replacement Therapy industry development trends and marketing channels are analyzed.

The research includes historic data from 2012 to 2016 and forecasts until 2022 which makes the reports an invaluable resource for industry executives, marketing, sales and product managers, consultants, analysts, and other people looking for key industry data in readily accessible documents with clearly presented tables and graphs. The report will make detailed analysis mainly on above questions and in-depth research on the development environment, market size, development trend, operation situation and future development trend of Testosterone Replacement Therapy on the basis of stating current situation of the industry in 2017 so as to make comprehensive organization and judgment on the competition situation and development trend of Testosterone Replacement Therapy Market and assist manufacturers and investment organization to better grasp the development course of Testosterone Replacement Therapy Market.

The study was conducted using an objective combination of primary and secondary information including inputs from key participants in the industry. The report contains a comprehensive market and vendor landscape in addition to a SWOT analysis of the key vendors.

Inquire before buying at: https://www.marketinsightsreports.com/reports/09271168/global-testosterone-replacement-therapy-market-research-report-2017/inquiry

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Source URL: https://marketersmedia.com/global-testosterone-replacement-therapy-market-overview-and-scope-2017-to-2022/243574

For more information, please visit https://www.marketinsightsreports.com/reports/09271168/global-testosterone-replacement-therapy-market-research-report-2017

Source: MarketersMedia

Release ID: 243574

SHAREHOLDER ALERT: Bronstein, Gewirtz & Grossman, LLC Announces Investigation of Adidas AG (ADDYY) (ADDDF)

NEW YORK, NY / ACCESSWIRE / September 28, 2017 / Bronstein, Gewirtz & Grossman, LLC is investigating potential claims on behalf of purchasers of Adidas. (“Adidas” or the “Company”) (OTCQX: ADDYY) (OTCQX: ADDDF). Such investors are encouraged to obtain additional information and assist the investigation by visiting the firm’s site: www.bgandg.com/addyy.

The investigation concerns whether Adidas and certain of its officers and/or directors have violated Sections 10(b) and 20(a) of the Securities Exchange Act of 1934.

On September 26, 2017, federal prosecutors unveiled fraud charges against 10 people associated with certain NCAA basketball programs, including four coaches and an Adidas executive. Prosecutors announced that they uncovered two related schemes, including one in which apparel executives, financial advisers and others bribed assistant college coaches to steer elite players to their programs, and a second in which players were allegedly bribed to enroll at schools sponsored by Adidas. On this news, Adidas’s share price fell $7.20, or 3.17%, to close at $220.00 on September 26, 2017.

If you are aware of any facts relating to this investigation, or purchased Adidas shares, you can assist this investigation by visiting the firm’s site: www.bgandg.com/addyy. You can also contact Peretz Bronstein or his Investor Relations Analyst, Yael Hurwitz of Bronstein, Gewirtz & Grossman, LLC: 212-697-6484.

Bronstein, Gewirtz & Grossman, LLC is a corporate litigation boutique. Our primary expertise is the aggressive pursuit of litigation claims on behalf of our clients. In addition to representing institutions and other investor plaintiffs in class action security litigation, the firm’s expertise includes general corporate and commercial litigation, as well as securities arbitration. Attorney advertising. Prior results do not guarantee similar outcomes.

Contact:

Bronstein, Gewirtz & Grossman, LLC
Peretz Bronstein or Yael Hurwitz
212-697-6484 | info@bgandg.com

SOURCE: Bronstein, Gewirtz & Grossman, LLC

ReleaseID: 476608

SHAREHOLDER ALERT: Lundin Law PC Announces Securities Class Action Lawsuit against Top Ships Inc. and Reminds Investors with Losses to Contact the Firm

LOS ANGELES, CA / ACCESSWIRE / September 28, 2017 / Lundin Law PC, a shareholder rights firm, announces a class action lawsuit against Top Ships Inc. (“Top Ships” or the “Company”) (NASDAQ: TOPS) for possible violations of federal securities laws from January 17, 2017 through August 22, 2017, inclusive (the “Class Period”). Investors, who purchased or otherwise acquired Top Ships shares during the Class Period, should contact the firm prior to the October 23, 2017 lead plaintiff motion deadline.

To participate in this class action lawsuit, click here.

You can also call Brian Lundin, Esq., of Lundin Law PC, at 888-713-1033, or you can e-mail him at brian@lundinlawpc.com.

No class has been certified in the above action yet. Until a class is certified, you are not considered to be represented by an attorney. You may also choose to do nothing and be an absent class member.

According to the Complaint, throughout the Class Period, CEO Evangelos J. Pistiolis caused the Company to engage in a series of manipulative share issuance and sales transactions with Kalani Investments Limited (“Kalani”) through which Top Ships would sell its common shares and securities convertible into common shares to Kalani at a significant discount to market price and file registration statements so that Kalani could resell these shares into the market. When Kalani’s sales of Top Ships stock caused its share price to decline, the Company would reverse split the stock, causing a certain number of outstanding shares to be merged into a single share, and thereby raise the price of its stock. Then, the Company would again sell securities to Kalani, and the same pattern of transactions would ensue. While Top Ships was engaging in these transactions, the Company failed to disclose the true purpose of the transactions and related stock issuances and reverses – to finance related-party transactions and acquisitions that primarily benefited Mr. Pistiolis and his related companies, and otherwise funnel money to Company insiders. By August 2017, Top Ships, through Kalani, issued and sold into the market tens of millions of shares of its common stock, vastly diluting the Company’s existing shareholders. While Top Ships used the proceeds from these offerings to further enrich Mr. Pistiolis and his affiliates through various related-party transactions, the value of Top Ships’ common stock has fallen by more than 99%, which caused investors harm.

Lundin Law PC was founded by Brian Lundin, Esq., a securities litigator based in Los Angeles dedicated to upholding shareholders’ rights.

This press release may be considered Attorney Advertising in some jurisdictions under the applicable law and ethics rules.

Contact:

Lundin Law PC
Brian Lundin, Esq.
Telephone: 888-713-1033
Facsimile: 888-713-1125
brian@lundinlawpc.com
http://lundinlawpc.com/

SOURCE: Lundin Law PC

ReleaseID: 476619

SHAREHOLDER ALERT: Lundin Law PC Announces Securities Class Action Lawsuit against Vitamin Shoppe, Inc. and Reminds Investors with Losses to Contact the Firm

LOS ANGELES, CA / ACCESSWIRE / September 28, 2017 / Lundin Law PC, a shareholder rights firm, announces a class action lawsuit against Vitamin Shoppe, Inc. (“Vitamin Shoppe” or the “Company”) (NYSE: VSI) for possible violations of federal securities laws from March 1, 2017 through August 6, 2017, inclusive (the “Class Period”). Investors, who purchased or otherwise acquired Vitamin Shoppe shares during the Class Period, should contact the firm prior to the October 27, 2017 lead plaintiff motion deadline.

To participate in this class action lawsuit, click here.

You can also call Brian Lundin, Esq., of Lundin Law PC, at 888-713-1033, or you can e-mail him at brian@lundinlawpc.com.

No class has been certified in the above action yet. Until a class is certified, you are not considered to be represented by an attorney. You may also choose to do nothing and be an absent class member.

According to the Complaint, throughout the Class Period, Vitamin Shoppe made false and/or misleading statements, and/or failed to disclose: that the Company’s retail segment was continuing to dramatically decline; that the Company’s ongoing “reinvention plan” had been unsuccessful and brought more than $168 million in goodwill impairment, and it was not properly recognizing that impairment charge; and that as a result of the above, the Company’s public statements were materially false and misleading at all relevant times. When this news was announced, Vitamin Shoppe’s stock price declined materially, which caused investors harm according to the Complaint.

Lundin Law PC was founded by Brian Lundin, Esq., a securities litigator based in Los Angeles dedicated to upholding shareholders’ rights.

This press release may be considered Attorney Advertising in some jurisdictions under the applicable law and ethics rules.

Contact:

Lundin Law PC
Brian Lundin, Esq.
Telephone: 888-713-1033
Facsimile: 888-713-1125
brian@lundinlawpc.com
http://lundinlawpc.com/

SOURCE: Lundin Law PC

ReleaseID: 476620

SHAREHOLDER ALERT: Lundin Law PC Announces Securities Class Action Lawsuit against Health Insurance Innovations, Inc. and Encourages Investors with Losses to Contact the Firm

LOS ANGELES, CA / ACCESSWIRE / September 28, 2017 / Lundin Law PC, a shareholder rights firm, announces the filing of a class action lawsuit against Health Insurance Innovations, Inc. (“Health Insurance Innovations” or the “Company”) (NASDAQ: HIIQ) for possible violations of federal securities laws between August 2, 2017 and September 11, 2017, inclusive (the “Class Period”). Investors, who purchased or otherwise acquired shares during the Class Period, should contact the firm prior to the November 10, 2017 lead plaintiff motion deadline.

To participate in this class action lawsuit, click here.

You can also call Brian Lundin, Esq., of Lundin Law PC, at 888-713-1033, or you can e-mail him at brian@lundinlawpc.com.

No class has been certified in the above action yet. Until a class is certified, you are not considered represented by an attorney. You may also choose to do nothing and be an absent class member.

According to the Complaint, throughout the Class Period, Health Insurance Innovations made false and/or misleading statements and/or failed to disclose: that the Company’s application for a third-party insurance administrators license with the Florida Office of Insurance Regulation was denied due partly to material errors and omissions; that the Florida Office of Insurance Regulation’s rejection of its application for a third-party insurance administrators license could result in loss of licenses in the other states; and as a result of the above, the Company’s public statements were materially false and misleading at all relevant times. When this news was announced, shares of Health Insurance Innovation fell in value materially, which caused investors harm according to the Complaint.

Lundin Law PC was founded by Brian Lundin, Esq., a securities litigator based in Los Angeles dedicated to upholding shareholders’ rights.

This press release may be considered Attorney Advertising in some jurisdictions under the applicable law and ethics rules.

Contact:

Lundin Law PC
Brian Lundin, Esq.
Telephone: 888-713-1033
Facsimile: 888-713-1125
brian@lundinlawpc.com
http://lundinlawpc.com/

SOURCE: Lundin Law PC

ReleaseID: 476621

DEADLINE MONDAY: Lundin Law PC Announces Securities Class Action Lawsuit against The Advisory Board Company and Reminds Investors with Losses to Contact the Firm

LOS ANGELES, CA / ACCESSWIRE / September 28, 2017 / Lundin Law PC, a shareholder rights firm, announces a class action lawsuit against The Advisory Board Company (“Advisory Board” or the “Company”) (NASDAQ: ABCO) for possible violations of federal securities laws from January 21, 2015 through February 23, 2016, inclusive (the “Class Period”). Investors, who purchased or otherwise acquired Advisory Board shares during the Class Period, should contact the firm by October 2, 2017, the lead plaintiff motion deadline.

To participate in this class action lawsuit, click here.

You can also call Brian Lundin, Esq., of Lundin Law PC, at 888-713-1033, or you can e-mail him at brian@lundinlawpc.com.

No class has been certified in the above action yet, and until a class is certified, you are not considered to be represented by an attorney. You may also choose to do nothing and be an absent class member.

According to the Complaint, throughout the Class Period, Advisory Board made materially false and/or misleading statements, and/or failed to disclose, that there were severe integration problems associated with its acquisition of Royall and, as a consequence, the Company had no basis to increase the revenue guidance for Royall during the Class Period. When this information went public, Advisory Board’s stock price fell materially, which caused investors harm according to the Complaint.

Lundin Law PC was established by Brian Lundin, Esq., a securities litigator based in Los Angeles dedicated to upholding shareholders’ rights.

This press release may constitute Attorney Advertising in certain jurisdictions under the applicable law and rules of ethics.

Contact:

Lundin Law PC
Brian Lundin, Esq.
Telephone: 888-713-1033
Facsimile: 888-713-1125
brian@lundinlawpc.com
http://lundinlawpc.com/

SOURCE: Lundin Law PC

ReleaseID: 476613

OCTOBER 3 DEADLINE: Lundin Law PC Announces Securities Class Action Lawsuit against Envision Healthcare Corporation and Encourages Investors with Losses to Contact the Firm

LOS ANGELES, CA / ACCESSWIRE / September 28, 2017 / Lundin Law PC, a shareholder rights firm, announces a class action lawsuit against Envision Healthcare Corporation (“Envision” or the “Company”) (NYSE: EVHC) for possible violations of federal securities laws from March 2, 2015 through July 21, 2017, inclusive (the “Class Period”). Investors, who purchased or otherwise acquired Envision shares during the Class Period, should contact the firm before the October 3, 2017 lead plaintiff motion deadline.

To participate in this class action lawsuit, click here.

You can also call Brian Lundin, Esq., of Lundin Law PC, at 888-713-1033, or e-mail him at brian@lundinlawpc.com.

No class has been certified in the above action yet, and until a class is certified, you are not considered represented by an attorney. You may choose to do nothing and be an absent class member as well.

The Complaint states that throughout the Class Period, Envision made materially false and/or misleading statements, and/or failed to disclose material information, to investors. On July 24, 2017, The New York Times published an article reporting that hospitals associated with the Company’s subsidiary, EmCare Holdings, Inc., were disproportionately likely to engage in “surprise billing,” in which patients seeking treatment at in-network facilities were treated by out-of-network physicians and then billed at higher rates. When this news went public, Envision’s share price fell materially, which caused investors harm according to the lawsuit.

Lundin Law PC was founded by Brian Lundin, Esq., a securities litigator based in Los Angeles dedicated to upholding shareholders’ rights.

This press release may be considered Attorney Advertising in certain jurisdictions under the applicable law and ethics rules.

Contact:

Lundin Law PC
Brian Lundin, Esq.
Telephone: 888-713-1033
Facsimile: 888-713-1125
brian@lundinlawpc.com
http://lundinlawpc.com/

SOURCE: Lundin Law PC

ReleaseID: 476614

AAOI INVESTOR ALERT: Lundin Law PC Announces Securities Class Action Lawsuit against Applied Optoelectronics, Inc. and Encourages Investors with Losses to Contact the Firm

LOS ANGELES, CA / ACCESSWIRE / September 28, 2017 / Lundin Law PC, a shareholder rights firm, announces a class action lawsuit against Applied Optoelectronics, Inc. (“Applied Optoelectronics” or the “Company”) (NASDAQ: AAOI) for possible violations of federal securities laws from July 13, 2017 through August 3, 2017, inclusive (the “Class Period”). Investors, who purchased or otherwise acquired Applied Optoelectronics shares during the Class Period, should contact the firm before October 4, 2017, the lead plaintiff motion deadline.

To participate in this class action lawsuit, click here.

You can also call Brian Lundin, Esq., of Lundin Law PC, at 888-713-1033, or you can e-mail him at brian@lundinlawpc.com.

No class has been certified in the above action yet. Until a class is certified, you are not considered to be represented by an attorney. You may also choose to do nothing and be an absent class member.

The Complaint states that during the Class Period, Applied Optoelectronics made false and/or misleading statements, and/or failed to disclose: that a major customer was decreasing its purchases of the Company’s 40G receivers; that the loss of this major customer’s business would have a severe negative impact on the Company’s financial performance; and that as a result, the Company’s public statements were materially false and misleading at all relevant times. When this news went public, Applied Optoelectronics’ stock price lowered materially, which caused investors harm according to the Complaint.

Lundin Law PC was founded by Brian Lundin, Esq., a securities litigator based in Los Angeles dedicated to upholding shareholders’ rights.

This press release may constitute Attorney Advertising in certain jurisdictions under the applicable law and rules of ethics.

Contact:

Lundin Law PC
Brian Lundin, Esq.
Telephone: 888-713-1033
Facsimile: 888-713-1125
brian@lundinlawpc.com
http://lundinlawpc.com/

SOURCE: Lundin Law PC

ReleaseID: 476615