Ervical Dysplasia Diagnostic Market 2019 Analysis and Precise Outlook - Abbott Laboratories, Roche Holding AG, Hologic, Inc., Micromedic Technologies Ltd

The report titled "Ervical Dysplasia Diagnostic Market" report will be very useful to get a stronger and effective business outlook. It provides an in-depth analysis of different attributes of industries such as trends, SWOT analysis, policies, and clients operating in several regions. The qualitative and quantitative analysis techniques have been used by analysts to provide accurate and applicable data to the readers, business owners and industry experts.

The Ervical Dysplasia Diagnostic market was valued at 12500 Milion US$ in 2019 and is projected to reach 17700 Million US$ by 2025, at a CAGR of 5.1% during the forecast period.

Cervical dysplasia, also known as cervical intraepithelial neoplasia (CIN), causes abnormal cell growth that occurs on the epithelial lining of the cervix.

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The report presents the market competitive landscape and a corresponding detailed analysis of the major vendor/key players in the market. Top Companies in the Global Ervical Dysplasia Diagnostic Market: Abbott Laboratories, Roche Holding AG, Hologic, Inc., Micromedic Technologies Ltd., PDS Biotechnology Corporation, Quest Diagnostics, Inc., QIAGEN N.V. and others.

News Update:

April 7, 2020 (Hologic)

Interested participants may listen to the call by dialing 888-204-4368 (in the United States and Canada) or +1 323-994-2093 (for international callers) and referencing access code 1336510. Participants should dial in 5-10 minutes before the call begins. A replay will be available approximately two hours after the call ends through Friday, May 22, 2020. The replay numbers are 888-203-1112 (U.S.) or +1 719-457-0820 (international), access code 1336510, PIN 1749.

APR 15 2020 (QIAGEN N.V.)

Colorectal cancer is the third most common type of cancer, and approximately 150,000 patients a year in the United States are diagnosed with CRC. In primary and metastatic CRC, BRAF mutations (nearly always V600E) are present in up to 15% of patients and are thought to be key drivers of tumor growth. Detection of the V600E mutation utilizing the therascreen BRAF V600E assays will help identify patients eligible for treatment with the newly approved combination of BRAFTOVI and cetuximab. The therascreen BRAF V600E kit runs on QIAGEN's Rotor-Gene Q MDx, a member of the modular QIAsymphony family of automation solutions.

Global Ervical Dysplasia Diagnostic Market Split By Product Type and Applications:

This report segments the global Ervical Dysplasia Diagnostic Market on the basis of Types are:
Diagnostic Test
Diagnostic Device

On the basis of Application, the Global Ervical Dysplasia Diagnostic Market is segmented into:
Hospitals
Clinic
Others

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Regional Analysis For Ervical Dysplasia Diagnostic Market:

For the comprehensive understanding of market dynamics, the global Ervical Dysplasia Diagnostic Market is analysed across key geographies namely: United States, China, Europe, Japan, South-east Asia, India and others. Each of these regions is analysed on the basis of market findings across major countries in these regions for a macro-level understanding of the market.

Important Features that are under Offering and Key Highlights of the Reports:

- Detailed overview of Ervical Dysplasia Diagnostic Market.
- Changing market dynamics of the Ervical Dysplasia Diagnostic Market industry.
- In-depth segmentation of Ervical Dysplasia Diagnostic Market by Type, Application etc.
- Historical, current and projected market size in terms of volume and value.
- Recent industry trends and developments.
- Competitive landscape of Ervical Dysplasia Diagnostic Market.
- Strategies of key players and product offerings.
- Potential and niche segments/regions exhibiting promising growth.

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Refrance and Source:

https://investors.hologic.com/press-releases/press-release-details/2020/Hologic-to-Announce-Financial-Results-for-the-Second-Quarter-of-Fiscal-2020-on-Wednesday-April-29-2020/default.aspx

https://corporate.qiagen.com/newsroom/press-releases/2020/20200415_braf_fda

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