Search Marketing Expo – London 2018

Search Marketing Expo – London 2018
Event on 2018-05-22 08:00:00
Immerse yourself in two days of SEO, SEM and Online Marketing sessions and you?re guaranteed to leave with practical tips and techniques to immediately improve your search marketing efforts. SMX also has strategic sessions to help you with what?s coming over the horizon.

With sessions designed to serve a diverse search marketing audience, you?ll discover topics tailored for your needs ? whether you?re into SEO or SEM, whether you?re an advanced search marketing veteran or are a beginner just learning the ropes.

The SMX agenda is created by the editors of Search Engine Land, the publication of record for search marketers. You get unbiased, vendor agnostic programming at SMX. You can be confident that you?ve invested wisely.

at etc. Venues, 155 Bishopsgate
Liverpool St.
City of London, United Kingdom

Raleigh SEO Conference 2018

Raleigh SEO Conference 2018
Event on 2018-05-15 09:00:00
Can you believe the Raleigh SEO Meetup is hosting our third annual conference?! Our attendees learn about content marketing, search engine optimization for local businesses, and advanced agency strategies. One of the unique features of this conference is that speakers from across the country and right here in the Research Triangle provide actionable advice in a small group setting. Participants are delighted to have more interaction with marketing experts than at other conferences. It doesn't matter if you're new to SEO and looking to increase your skills or if you're an SEO agency owner, there's something here for everyone to learn. 2018 Raleigh SEO Meetup Conference This year we will have three tracks and 9 sessions covering the basics of online marketing and delving into the depths of agency management. We will also have keynotes from Jenny Halasz and Ashley Berman Hale! While the speaker lineup for 2018 is still being decided, past speakers have included: Phil Buckley Director of Technical SEO at Adapt, one of the Moz recommended companies in Raleigh JR Oakes Director of Strategy at ConsultWebs Patrick Stox SEO Specialist at IBM Karl Sakas Agency Consultant at Sakas & Company Will Hardison Agency Owner at FanBase Content Marketing & Social Media You know that content is king, but you're still trying to figure out how to create great content. More important than that, you need to know how to connect that content with the bottom line for your business – sales. These sessions will show you how to use written content, videos, photography, social media and more to connect with your audience online. You will come away with a wealth of ideas to drive engagement and sales in your business or for your clients. Local SEO & Voice Search While everyone needs to have an online presence today, not all businesses serve customers around the globe. Those that are trying to connect with people online that live in their neighborhood will benefit from a leason in local SEO. Do you know how to optimize the content on your website for personal digital assistants like Alexa? Are you closing deals after your business is found in search results? This is the track for you if your business, or your client's business, needs to stand out as a local provider in a global marketplace. Advanced Panel Discussions Do you count yourself among the most knowledgable marketing experts at any conference? Then this is the track for you. We've collected panels of agency owners and senior staff to answer your questions. This is your opportunity to geek out about online marketing and SEO with your peers. Learn what it takes to overcome the biggest challanges faced by marketing agencies around the world. The Latest Conference Details Visit RaleighSEOconference.com

at Nature Research Center Store
121 West Jones Street
Raleigh, United States

FDA Audit Checklist Clinical Trials Seminar 2018

FDA Audit Checklist Clinical Trials Seminar 2018
Event on 2018-04-26 09:00:00
Course "Managing Your FDA Inspection: Before, During and After" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: FDA's inspection program follows well-established procedures and conducts the inspections with as much consistency as possible. FDA trains its investigators from day one. During the first six months, they attend extensive classroom and hands on training. FDA investigators learn basic skills. As time goes on, special training is given and the field staff use detailed reference materials to guide their thinking, actions, decisions and conclusions. If you understand FDA's management of its investigators and inspectional process, you can keep your establishment ahead of a needless regulatory disaster. FDA conducts inspections with standard operating procedures and detailed information on how to handle almost any situation the FDA investigator may face. The course will let you see inside an FDA investigator's mind set and what the agency will do when it evaluates what the investigator says and documents. What the investigator does and what FDA does are not mysteries, they just seem like it. Why you should attend: "Hi, I'm from the FDA and here to conduct an inspection." What is the first thing you do? Ring a fire alarm, close down for the day (some firms have) or do you follow well-planned protocol. You think, "Why is FDA here? Are we in trouble?" Are you prepared to talk about the trouble you know you have with FDA regulations or is your plan of action to cross your fingers. We all know that a bad FDA inspection has immediate and long-term consequences. The cost of fixing your problems, the bad public relations, upset customers and future business plans can be set into a downward spiral. If you do not understand what FDA is doing or thinking, how can you expect to deal successfully with FDA? If you don't know how to anticipate an investigator's actions or follow their train of thought, you will not be able to mitigate the effect of inspectional findings. "Is FDA going to send us a Warning Letter?" You can make a reasonable prediction if you understand your inspectional results and how FDA will "grade" it. The tools are available. Areas Covered in the Session FDA legal authorityTypes of inspectionsFDA investigator trainingFDA's written procedures, policy and operations guideIndustry inspection protocolWhat to do and not do during an inspectionForm FDA 483 responseWarning Letter responseEnforcement Who Will Benefit: Regulatory AffairsQuality AssuranceManufacturing Agenda: Day 1 Schedule Lecture 1: FDA Inspection authority FDA Inspection authorityInspectional refusal prohibition Lecture 2: Types of Inspections: purpose, scope and scrutiny Comprehensive GMPAbbreviated GMPDistrict or Center DirectedRegulatory Follow-upSurveillanceLimitedFor Cause Lecture 3: Impact on you during and after inspection How to interact with the FDA investigatorWhat not to say and doYour protocolMismanagement of the inspection Lecture 4: FDA Investigator Training – This is what they are thinking On the job training and supervisionTechnical, classroom and mock inspectionsEvidence development to tell the storyPhysical and documentary samples of your violationsWriting reports, inspectional observations and sample documentationPhysical threats and assault Lecture 5: Investigations Operations Manual Procedures and technical guidance. FDA's rules for themselvesFDA organization chart "in the field." Who is watching you? Compliance Programs Section III – the inspection / specific issuesSection V – the regulatory response / risk assessment Lecture 6: Investigations Operations Manual (continued) Writing inspectional observations (Form FDA 483)Writing establishment inspection reportsEvidence documentation and custody Mock "Limited" inspection Day 2 Schedule Lecture 1: FDA Form 483 – List of objectionable conditions, aka list of observations PurposeFormat / organizationManaging 483 observations during the inspectionResponding to 483 observations during "discussion with management" What it meansHow to manage the discussionHow to challenge a 483 observationWhat to say and not say Lecture 2: Your written response to a 483 Understanding the 483 – using an FDA issued 483Time deadlinesStrategy for corrections and corrective actionEvidence of corrections and corrective actionEmpty promises Lecture 3: FDA Warning Letter – advisory of possible legal action FDA Warning Letter proceduresResponding to a Warning Letter – in 15 working days. Group Hypothetical Warning Letter Response – in 10 minutes Lecture 4: FDA Enforcement Actions Judicial SeizureInjunctionProsecutionMonetary penalties Administrative Import / ExportGovernment contractsOther government agency advisoriesFinesPremarket holds Speaker Casper Uldriks ex-FDA Expert and former Associate Center Director of CDRH Casper (Cap) Uldriks owns Encore Insight LLC, which provides consulting services on FDA Law. He brings over 32 years of experience from the FDA. He specialized in the FDA's medical device program as a field investigator, served as a senior manager in the Office of Compliance and as an Associate Center Director for the Center for Devices and Radiological Health. He developed enforcement actions and participated in the implementation of new statutory requirements. He is recognized as an exceptional and energetic speaker. His comments are candid, straightforward and of practical value. He understands how FDA thinks, operates and where it is headed. Location: Seattle, WA Date: April 26th & 27th, 2018 and Time: 9:00 AM to 6:00 PM Venue: Courtyard Seattle Sea-Tac Area 16038 West Valley Highway Tukwila Washington 98188 USA Price: Register now and save 0. (Early Bird) Price: ,295.00 (Seminar Fee for One Delegate) Until March 10, Early Bird Price: ,295.00 From March 11 to April 24, Regular Price: ,495.00 Register for 5 attendees Price: ,885.00 ,475.00 You Save: ,590.00 (40%)* Register for 10 attendees Price: ,122.00 ,950.00 You Save: ,828.00 (45%)* Sponsorship Program benefits for “Quality Assurance Auditing for FDA Regulated Industry” seminar At this seminar, world-renowned FDA Regulated Industry subject matter experts interact with CXO’s of various designations. Executives who carry vast experience about FDA Regulated Industry and Experts get down to discussing industry-related best practices, regulatory updates, changes in technologies, and much more relating to FDA Regulated Industry. As a sponsor of these seminars, you get the opportunity to have your product and company reach out to C-Level executives in FDA Regulatory -related industries and become known among these elite executives and subject matter experts. Apart from being seen prominently at these globally held seminars, you also get talked about frequently in our correspondences with our experts and these participants. For More Information- https://www.globalcompliancepanel.com/control/sponsorship Contact us today! NetZealous LLC DBA GlobalCompliancePanel john.robinson@globalcompliancepanel.com support@globalcompliancepanel.com Toll free: +1-800-447-9407 Phone: +1-510-584-9661 Website: http://www.globalcompliancepanel.com Registration Link Follow us on LinkedIn: https://www.linkedin.com/company/globalcompliancepanel/ Like us our Facebook page: https://www.facebook.com/TrainingsAtGlobalCompliancePanel/ Follow us on Twitter: https://twitter.com/GCPanel Early Bird – Seminar Fee for One Delegate – 95.00 Regular Price – 95.00 Register for 5 attendees – 85.00 Register for 10 attendees – 22.00

at Courtyard Seattle Sea-Tac Area
16038 West Valley Highway Tukwila Washington 98188 USA
Seattle, United States

USA Trade Tasting 2018

USA Trade Tasting 2018
Event on 2018-05-15 11:00:00
USA Trade Tasting is a 2-day event being held from 15th May to 16th May 2018 at the Metropolitan Pavilion in New York, United States Of America. This event showcases products like producers connect with wine, beer, spirits importers, distributors, retailers and press, the event is B2B ONLY with the sole purpose of exhibiting brands to connect with new buyers and vice-versa etc. in the Wine, Beer & Spirits industries.

About USATT Organizer – Beverage Trade Network
Beverage Trade Network (BTN) is a leading online marketing and B2B networking platform servicing suppliers, buyers and beverage professionals in the global beverage industry. BTN provides a selection of sourcing solutions for importers and distributors as well as an extensive range of marketing and distribution services for international suppliers. BTN also runs a line-up of b2b trade shows around the world. For more information about BTN, please visit www.beveragetradenetwork.com

Email: info@usatradetasting.com
Phone No.: +1 855 481 1112

at Metropolitan Pavillion
125 W 18th St, New York, NY 10011
Wilmington, United States

Verification vs. Validation – Product Process Software and QMS 2018

Verification vs. Validation – Product Process Software and QMS 2018
Event on 2018-01-22 09:00:00
Course "Verification vs. Validation – Product Process Software and QMS" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: This course will review the company Master Validation Plan for major key inputs and CGMP deficiencies. It will address the FDA's newer and tougher regulatory stance. This course's aim is to prove "Product Risk Based V&V" by sufficient, targeted and documented risk-based V&V test case elements/scripts. It will teach participants to evaluate its elements against ISO 14971 and ICH Q9 for hazard analysis and product risk management. This course will evaluate different field-tested, U.S. FDA-reviewed V&V protocols; how to employ equipment/process Requirements Specs / DQs, IQs, OQs, and PQs, or their equivalents per ASTM E2500, all against a background of limited company resources. It will review a matrix that simplifies "as-product", in-product", process and equipment, et al, software VT&V, to assure key FDA requirements are not overlooked. While considering the QMS and 21 CFR Part 11; this course will make practical application of these same in two hands-on sessions. Why you should attend: This session helps participants: Understand Verification and Validation, differences and how they work together;Discuss recent regulatory expectations;Know how to document a "risk-based" rationale, and use it in a resource-constrained environment;Determine key "milestones" and "tasks" in a project;Locate and document key subject "inputs";Compile "generic" Master and Individual Validation Plans;Learn the key element of a Product V&V File/Protocol;Understand how to develop Process and/or Production/Test Equipment V&V Files/Protocols;Get a grasp of basic Test Case construction;Understand sample sizes and their justification;Learn the key elements of Software V&V expected by the FDA and how to document;Deal with hardware and software vendors, sales and marketingConsider a field-tested software V&V documentation "model";See how to compile QMS Electronic Records and Electronic Signatures V&Vs to satisfy 21 CFR Part 11. Who will benefit: This workshop will provide valuable assistance to all regulated companies that need to review and modify their Master Validation Planning and V&V activities / plan(s). This information addresses Medical Devices, Pharmaceutical, Diagnostic, and Biologics requirements and implementation. The employees who will benefit include: Senior and middle management and staffRegulatory AffairsQuality Assurance or Quality Control ProfessionalsQA/QCIT/ISR&DProduction ManagementManufacturing EngineersProcess EngineersSoftware EngineersProject ManagersHardware and software vendors, sales and marketingAny professional tasked with V&V responsibilities Agenda: Day 1 Schedule Lecture 1: Master Validation Planning and the Master Validation Plan(s) Lecture 2: Product, Process / Equipment Hardware V&V Lecture 3: Product / Device V&V Lecture 4: Software V&V Lecture 5: Quality Management System / 21 CFR Part 11 V&V Lecture 6: Summary of morning discussion Lecture 7: Group activity on the MVPs Lecture 8: Review of group activity and Q&A Day 2 Schedule Lecture 1: Software V&V documentation "model" Lecture 2: Software V&V protocols – "black box", "white box" Lecture 3: Electronic Records and Electronic Signatures (Part 11) Lecture 4: Summary of morning discussion Lecture 5: Group activity on 1) hardware / equipment, and 2) software V&V protocols Lecture 6: Review of group activity and Q&A Lecture 7: Course summary discussion Lecture 8: Summary of morning discussion Lecture 9: Group activity on the MVPs Lecture 10: Review of group activity and Q&A Speaker John E Lincoln Consultant, Medical device and Regulatory affairs, John E Lincoln is Principal of J. E. Lincoln and Associates LLC, a consulting company. John, a graduate of UCLA, is a medical device and Regulatory Affairs consultant. He has helped companies to implement or modify their GMP systems and procedures, product risk management and U.S. FDA responses. In addition, he has successfully designed, written and run all types of process, equipment and software qualifications/validations, which have passed FDA audit or submission scrutiny, and have been described in peer-reviewed technical articles and workshops worldwide. John has also managed pilot production, regulatory affairs, product development/design control, 510(k) submissions and risk management per ISO 14971 and implemented projects. With over 28 years of experience in the FDA-regulated medical products industry, he has worked from start-ups to Fortune 100 companies, including Abbott Laboratories, Hospira, and Tyco/Mallinckrodt. Location: St. George UT Date: January 22nd & 23rd, 2018 and Time: 9:00 AM to 6:00 PM Venue: Hilton Garden Inn St. George 1731 South Convention Center Drive, Saint George, Utah, 84790, USA Price: Price: ,295.00 (Seminar Fee for One Delegate) Register now and save 0. (Early Bird) Until January 01, Early Bird Price: ,295.00 From December 31 to January 20, Regular Price: ,495.00 Register for 5 attendees Price: ,885.00 ,475.00 You Save: ,590.00 (40%)* Register for 10 attendees Price: ,122.00 ,950.00 You Save: ,828.00 (45%)* Sponsorship Program benefits for “Quality Assurance Auditing for FDA Regulated Industry” seminar At this seminar, world-renowned FDA Regulated Industry subject matter experts interact with CXO’s of various designations. Executives who carry vast experience about FDA Regulated Industry and Experts get down to discussing industry-related best practices, regulatory updates, changes in technologies, and much more relating to FDA Regulated Industry. As a sponsor of these seminars, you get the opportunity to have your product and company reach out to C-Level executives in FDA Regulatory -related industries and become known among these elite executives and subject matter experts. Apart from being seen prominently at these globally held seminars, you also get talked about frequently in our correspondences with our experts and these participants. For More Information- https://www.globalcompliancepanel.com/control/sponsorship Contact us today! NetZealous LLC DBA GlobalCompliancePanel john.robinson@globalcompliancepanel.com support@globalcompliancepanel.com Toll free: +1-800-447-9407 Phone: +1-510-584-9661 Website: http://www.globalcompliancepanel.com Registration Link – http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901450SEMINAR?ticketleap-January-2018-SEO Follow us on LinkedIn: https://www.linkedin.com/company/globalcompliancepanel/ Like us our Facebook page: https://www.facebook.com/TrainingsAtGlobalCompliancePanel/ Follow us on Twitter: https://twitter.com/GCPanel Seminar Fee for One Delegate – 95.00

at The Hilton Garden Inn
1731S.ConventionCenterDrive
Saint George, United States

2018 happyfishkidyoga Bi-weekly Kid Yoga Class (Sat/Sun) at Shah Alam

2018 happyfishkidyoga Bi-weekly Kid Yoga Class (Sat/Sun) at Shah Alam
Event on 2018-06-01 10:00:00
Children derive enormous benefits from yoga. Physically, it enhances their flexibility, strength, coordination, and body awareness. In addition, their concentration and sense of calmness and relaxation improves. Doing yoga, children exercise, play, connect more deeply with the inner self, and develop an intimate relationship with the natural world that surrounds them. Yoga brings that marvelous inner light that all children have to the surface.~ Yoga Journal

happyfishkidyoga bi-weekly children yoga class provides an wonderful opportunity for kids to learn connect to themselves and others through yoga. The class covers yoga postures, breathing techniques, mindfulness activities, quiet Time exercise, creative storytelling & etc.
Age group : 4 yo – 11yo

Bi-weekly (Saturday)
================
Jan 6 & 20
Feb 3 & 10
Mar 3 & 17
Apr 7 & 21
May 5 & 19
June 2 & 23

Time slot : 10am-11.30am

Bi-weekly (Sunday)
================
Jan 7 & 21
Feb 4 & 11
Mar 4 & 18
Apr 8 & 22
May 6 & 20
June 3 & 24

Time slot : 9.30am – 11.00am
11.30am – 1.00pm

2018 Class Fee :
a) Single class =RM30
b) Monthly Fee (2 Classses) = RM50
c) Quarterly Fee (6 /4 Classes*) = RM120 /RM80*

*ONLY 4 Classes for Q4 (Oct & Nov), no classes in December.

How to Register
==============
a) Kindly click going in facebook event and fill up our google form https://goo.gl/forms/x9zu4W85NVBEyqYb2

or
b) PM to our facebook page ( happyfishkidyoga ) or email happyfishyoga@gmail.com

c) For first timer, we would request your payment before the class starts to secure your slot.

Things to bring
============
a) Yoga Mat
b) Drinking water

What to wear
===========
Simple and comfortable.

Location
=======
The class will be conducted at my condo home studio [PRIMA U! ] which located Seksyen U1/Glemarie/Batu Tiga, Shah alam

Accessibilities:
– Federal Highway
– LKSA Highway
– Kesas Highway
– Sek 7 Shah Alam
– Shah Alam city center
Nearby
– 5 minutes walking to the lBatu Tiga commuter station.
– 10 minutes to Uitm Shah Alam, Jakel, Ariani,I-City
– 30 minutes to KL
– 35 minutes to KLIA
– 1km from Shah Alam City Center
– 5km from Subang Jaya, USJ & Bandar Sunway
– 8km from Klang
– 13km from Puchong
– 16km from Damansara, Petaling Jaya
– 20km from Sg. Buloh
– 28km from Kuala Lumpur

Abut the teacher
============
Shi is a kids yoga teacher, artisan, storyteller and meditator. She attained Complementary Health Education Diploma in Yoga Teaching (C.H.Ed Dip Yoga),UK in 2008,Certification in Basic Kids Yoga Teacher Training (Rainbow abc Taiwan) in 2012 and Intermediate Teacher Training in 2015 and Advance level in 2017. She also completed Yoga for the Special Child® LLC Basic 1 & 2 Program (95 hours) in 2012 at India which encompassing Basic Yoga Therapy techniques and teaching methods to enhance the natural development of infants, children and adults with special needs. A Certification in Baby Yoga Teacher Training in 2015. . Before that, Shi has earned her MBA (International) at Nottingham University, UK, yet, with her passion & love in yoga, she left her corporate job in 2011 & establish happyfishyoga with the little inspiration to build a career which she passionate about and to propound the healthy yogic lifestyle to the public especially children yoga. Shi has been actively and continuing involved in teaching and advocating kids yoga in Malaysia since 2012. She is also the key initiator, producer and organizer of the very first big kids yoga event which happened in 2016 namely Malaysia KL Kids Yoga Festival. Apart kids yoga, Shi also teaches yoga for children with special needs, kids quiet time exercise, mindfulness, yoga education in school, peace mama, family yoga, parent and kid yoga,creative storytelling & etc.

We will provide you the full address upon registration.

at Prima U1 Codo, Shah Alam

Shah Alam, Malaysia

Meia Maratona de Lisboa – 2018

Meia Maratona de Lisboa – 2018
Event on 2018-03-11 10:00:00
A Meia Maratona de Lisboa sempre tem como objetivo que novos recordes mundiais sejam alcançados, com uma largada exclusiva para a Elite, em Algés, e não na Ponte 25 de Abril, de onde parte o grosso do pelotão. Os dois grupos se juntam em Alcântara. Ao som de um fado, a largada da Meia Maratona e da Mini Maratona (8 km) acontecem simultaneamente, separadas por poucos metros de distância.  O percurso é bastante rápido, com largada e chegada em dois pontos diferentes, o que faz desta prova uma das mais atrativas do mundo. Pacote Exclusivo Período: 09 a 14 de Março – 5 noites de hospedagem em hotel selecionado (excelente localização)- Café da manhã- Transfer privativo Aeroporto / Hotel / Aeroporto- Ticket de 2 dias em ônibus turismo (hop on/hop off)- Seguro de viagem internacional para o período- Kit de Viagem MNM (Mochila, Camiseta..) Valores por pessoa: Hotel Restauradores 3*Quarto Duplo: EUR 429,00Quarto Individual: EUR  669.00 Hotel Borges Chiado 3*Quarto Duplo: EUR 479,00Quarto Individual: EUR  769.00 Hotel Feeling Chiado 3* SuperiorQuarto Duplo: EUR 509,00Quarto Individual: EUR  829.00 Hotel Turim Terreiro do Paço 4*Quarto Duplo: EUR 729,00Quarto Individual: EUR  1.269.00 Inscrição na Prova: EUR 55,00 (21k ou 8k) Formas de Pagamento:Em até 12x sem juros nos cartões de crédito. Consulte extensão da sua viagem para Porto, Madrid, Barcelona, Paris.. Consulte preço de passagem aérea promocional a partir da sua cidade consoco.

at Barcelona, Spain

Barcelona, Spain

Friends of Search 2018

Friends of Search 2018
Event on 2018-02-08 09:00:00
Friends of Search 2018: Hét search congres met toegang tot de belangrijkste, internationale ontwikkelingen in de wereld van search. Na vier succesvolle edities van Friends of Search afgelopen jaren vindt op donderdag 8 februari 2018 de alweer 5de editie plaats. Met diverse sprekers uit binnen- en buitenland is Friends of Search hét nationale search congres waar de laatste ontwikkelingen op SEO- en SEA-gebied aan bod komen. Je hoeft als (online) marketeer niet meer uit te wijken naar het buitenland als het om SEO- en SEA-congressen gaat. Friends of Search haalt searchexperts uit landen als Engeland, Duitsland en de VS, waar de ontwikkelingen vaak sneller gaan, naar Amsterdam om hun kennis en ervaring te delen. Na donderdag 8 februari 2018 weet je als bezoeker hoe andere organisaties zoekmachinemarketing en zoekmachineoptimalisatie inzetten en je bent ook op de hoogte van de belangrijkste, internationale ontwikkelingen in de wereld van search engine marketing. Voor wie? Friends of Search is bedoeld voor ervaren (online) marketeers en SEO- en SEA-specialisten aan de adverteerderszijde, die interesse hebben voor de veranderingen die nationaal en internationaal plaatsvinden in de wereld van search engine marketing. Maar ook voor specialisten aan bureauzijde is het evenement interessant, op donderdag 16 februari kunnen zij toetsen of ze nog in de pas lopen met de laatste ontwikkelingen.

at Kromhouthal

Amsterdam, Netherlands

Seeds Market Expected to Reach $85.2 Billion by 2018 – Report by MarketsandMarkets


Dallas, TX (PRWEB) December 27, 2014

According to a new market research report Seeds Market – Global Trends and Forecast to 2018, the Seeds Market will grow from $ 44,122.2 Million in 2012 to $ 85,237.6 Million by 2018 with a CAGR of 12.1% from 2013 to 2018. North America led the global market followed by Europe and Asia-Pacific in terms of revenue in 2012.

Make an Inquiry:

http://www.marketsandmarkets.com/Enquiry_Before_Buying.asp?id=376

Browse 157 market data tables and 22 figures spread through 383 pages and in-depth TOC on Seeds Market – Global Trends &Forecast To 2018.

http://www.marketsandmarkets.com/Market-Reports/seeds-market-376.html

Early buyers will receive 10% customization on this report.

Seed: Global Market

The seed market is categorized into four parts: oilseed includes soybean, sunflower, cotton, canola; grain seed includes corn, wheat, rice, millet crops; fruit & vegetable includes tomato, melon, carrot, onion, pepper, lettuce; other seed include alfalfa, turf, clover &f orage plants, and flower seed. The seed market is considered to be one of the most important segments of agriculture due to the rising food demand. Biotech seeds are consequently seen as those products which can improve the return on investment and respond to consumer demands for healthier and economical agricultural products by increasing per unit seed production and per hectare production.

North America: The largest Market for Seed

North America generated maximum revenue in the global seed market. Europe is the second largest market and Asia-Pacific stands third. U.S. drives the North American market while India and China drive the Asia-Pacific seed market. France generated maximum revenue in the European market, followed by Germany. Latin American market led by Brazil and ROW is also given a boost by the promising growth in South African countries.

Speak to Analyst:

http://www.marketsandmarkets.com/speaktoanalyst.asp?id=376

Grain seed: Biggest Market Segment

Grain seed controls the largest market share with corn as the most dominating crop in grain segment. The application of modern biotech trait seeds is driving the expansion of food production and new product development with increased nutritional values. Further insect and virus resistant seeds are developed to minimize crop losses and amplify production rate.

The report also studies various other important aspects of the market. It includes SWOT analysis, Porters analysis, the competitive landscape, and the patent analysis. In addition, 20 key players of this market have also been profiled with their current developments and growth strategies.

Browse Related Reports:

Seed Treatment Market – Global Trends, Forecasts and Technical Insights up to 2019

http://www.marketsandmarkets.com/Market-Reports/seed-treatment-market-503.html

Seed Coating Materials Market – Global Trends and Forecasts to 2019

http://www.marketsandmarkets.com/Market-Reports/seed-coating-materials-market-149045530.html

About MarketsandMarkets

MarketsandMarkets is the worlds No. 2 firm in terms of annually published premium market research reports. Serving 1700 global fortune enterprises with more than 1200 premium studies in a year, MarketsandMarkets is catering to multitude of clients across 8 different industrial verticals. We specialize in consulting assignments and business research across high growth markets, cutting edge technologies and newer applications. Our 850 full time analysts and SMEs at MarketsandMarkets are tracking global high growth markets following the “Growth Engagement Model GEM”. The GEM aims at proactive collaboration with the clients to identify new opportunities, identify most important customers, write “Attack, avoid and defend” strategies, and identify sources of incremental revenues for both the company and its competitors.

MarketsandMarketss flagship competitive intelligence and market research platform, “RT” connects over 200,000 markets and entire value chains for deeper understanding of the unmet insights along with market sizing and forecasts of niche markets. The new included chapters on Methodology and Benchmarking presented with high quality analytical info graphics in our reports gives complete visibility of how the numbers have been arrived and defend the accuracy of the numbers.

We at MarketsandMarkets are inspired to help our clients grow by providing apt business insight with our huge market intelligence repository.

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Blog: http://www.marketsandmarketsblog.com/market-reports/agriculture-industry







AMC CPU Cards Market to Grow at 21.31% CAGR by 2018 Forecasts a New Research Report at ReportsnReports.com

Dallas, Texas (PRWEB) November 30, 2014

Printed circuit boards which follow a specification of the PICMG are known as AMC (Advanced Mezzanine Cards). AMC is targeted to requirements for the next generation of “carrier grade” communications equipment and they are designed in such a way that they can work on any carrier card. AMC product standards are designed to support AdvancedTCA and MicroTCA systems. With the popularity of hot swapping among end-users and vendors, the global market for AMC CPU cards has grown steadily. The global AMC CPU cards market is forecasted to grow at a compound annual growth rate of 21.31 percent from 2014 to 2018. One of the key factors propelling the growth of AMC CPU cards market is the wide range of connectivity to the backplane and front panel provided by AMC, delivering high speed and flexible I/O support. AMCs offer serial interfaces and support various transport systems such as PCI express, GigE, and 10 gigabit Ethernet. Increased adoption of advanced TCA platforms integrated with AMC modules by TEMs and emerging initiatives in the aerospace and defense sector are also key drivers in the market.

Key players in the global market for AMC CPU cards are Emerson Network Power, Extreme Engineering Solutions Inc., Mercury Systems Inc. and Kontron AG. Other prominent vendors in the market include GE Intelligent Platforms, Adax Inc. and Advantech Corp. The global AMC CPU cards market has been segmented on the basis of application and geographical areas. On the basis of application, the global AMC CPU cards market can be divided into industrial automation and control, communications and network infrastructure, healthcare, military and aerospace, and transportation (including infotainment infrastructure). AMCs offer certain design advantages such as mobility, ruggedness, high-end processing and flexibility. Growing adoption of AdvancedTCA by telecom equipment manufacturers to reduce cost structure and time has accelerated the growth of AMCs deployed in ATCA. Changing technological requirements is one of the main challenges in the global AMC CPU cards market.

The report Global AMC CPU Cards Market 2014-2018 is an in-depth and professional report that covers market overview, market size and forecast, trends, opportunities, threats, challenges, drivers and their impact, growth prospect, prominent vendors, strength and weaknesses of the key vendors.

Order a copy of this report at (Prices start at US $ 2500 for a single user PDF) http://www.reportsnreports.com/purchase.aspx?name=318746.

List of Exhibits:

Exhibit 1: Market Research Methodology

Exhibit 2: ATCA System Architecture

Exhibit 3: Key Benefits and Features of AMC CPU Cards

Exhibit 4: Global AMC CPU Cards Market 2013-2018 (US$ million)

Exhibit 5: Global AMC CPU Cards Market by Application Segmentation 2013-2018

Exhibit 6: Global AMC CPU Cards Market by Application Segmentation 2013-2018 (US$ million)

Exhibit 7: Global AMC CPU Cards Market by Geographical Segmentation 2013-2018 (CAGR)

Exhibit 8: Global AMC CPU Cards Market by Geographical Segmentation 2013-2018

Exhibit 9: Global AMC CPU Cards Market by Geographical Segmentation 2013-2018 (US$ million)

Exhibit 10: Kontron: Business Segmentation by Revenue 2013

Exhibit 11: Kontron: Business Segmentation by Revenue 2012 and 2013 (US$ million)

Exhibit 12: Kontron: Geographical Segmentation by Revenue 2013

Exhibit 13: Mercury Systems: Business Segmentation by Revenue 2014

Exhibit 14: Mercury Systems: Business Segmentation by Revenue 2013 and 2014 (US$ million)

Exhibit 15: Mercury Systems: Geographical Segmentation by Revenue 2014

Exhibit 16: Extreme Engineering Solutions: Product Segmentation

Other New Reports on IT & Telecommunication Market:

IT Outsourcing Market in China 2014-2018: Analysts forecast the IT Outsourcing Market in China to grow at a CAGR of 25.01 percent over the period 2013-2018.

The IT Outsourcing market in China can be segmented into two divisions: Application Outsourcing and Infrastructure Outsourcing.

Key Companies: Accenture, Digital China Holding, Fujitsu, HP, IBM, Beyondsoft, ChinaSoft international, China Data Group (Suzhou), Dalian Hi-Think Computer Technology, HiSoft Technology International, Insigma, ISoftstone, Inspur Group, Longtop, Neusoft, Pactera, VanceInfo Technologies, WuXi AppTec, Yonyou.

Global Bank IT Spending Market 2014-2018: Analysts forecast the Global Bank IT spending market to grow at a CAGR of 4.75 percent over the period 2013-2018.

The Global Bank IT spending market can be segmented into three: Hardware, Third-party Software, and Services. This report provides data of the Global Bank IT Spending market in terms of product and geography.

Key Companies: Dell, HP, IBM, Microsoft, Accenture, ATOS, Capgemini, CGI Group, Cisco System, Cognizant, CSC, EMC, FIS, Fujitsu, HCL, Hitachi, Infosys, Intel, Logica, Oracle, SAP, TCS, Temenos, Teradata, Unisys and Wipro.

Explore other new reports by Infiniti Research Limited .

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