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Comfort Inn

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 155 Samoset St. , Plymouth, MA, US, 02360

  • Phone: (508) 746-2800
  • Fax: (508) 746-3485
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4.0 out of 5 (145 reviews)
81% of guests recommend this hotel

Attractions

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Haymarket
Faneuil Hall MarketplaceJanuary 30, 2015 6:00 AM
4 South Market Building
Boston, MA 02109
This outdoor market near Faneuil Hall carries on amid the din and confusion of Boston's Big Dig project. The wide selection of fresh produce and fish is available every Friday and Saturday, year-round, rain or shine from dusk until dawn. The market tends to get crowded but that adds to its charm. Expect to get some good deals, prices are less expensive than you would pay in a store. This weekly event is a magnet for photographers trying to capture the "real" Boston. Cash only.
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Statement.fridays @ Minibar
MinibarJanuary 30, 2015 10:00 PM
51 Huntington Avenue
Boston, MA 02116
Join us and help us usher in this latest addition to the Boston nightlife scene!  Statement Fridays is a night that will cater to and bring together some of the citiest most upbeat, energetic and fashionable crowd. Mingle and connect with like minded individuals, who like you, have been on the lookout for a venue that could serve as a destination for all matters that promise to defy the otherwise weekly stagnant scene. The evening's soundtrack will be provided by our resident DJ, Miss Camila Fabb ! Additional Information: - Kindly note this is a limited capacity weekly event.   - Admission is by RSVP and/or Tables only.  - Dress code is enforced. - RSVP is valid until 11:15pm. - Time: 10pm-2am - NO cover. - Dinner menu is available. -  Valet services available.  For further information regarding table packages or any other questions related to the event, please feel free to reach the Event Executive at 857-264-1321
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Six Sigma Green Belt Certification Training Workshop | Instructor Led Six Sigma Training Bootcamp In Boston, Ma On 27th Jan-30th Jan 2015 | Register Now At $499
BostonJanuary 30, 2015 8:00 AM
Boston
Boston, MA 02108
Six Sigma Green Belt Training Classroom Workshop is an instructor-led Live Online classroom training program which will help you in understanding different concepts of Six Sigma Green Belt theories and how to implement the same at your work to improve the quality and performance of your work.   Click here for our calendar of upcoming Six Sigma Training Sessions About CourseRAFT CourseRAFT is a Certification and Training Organization imparting training on Quality and Operations, Data Analytics, Project Management and IT Management. We have trained 10,000+ professional across globe. Our Trainings are provided by Leading Trainers with Experience of more than 12 years. Click here to know more. Six Sigma Green Belt Course Kit: 4 Days of intense classroom training by an Well Experienced Certified Faculty Member Lean Six Sigma Green Belt certification Fee included Prepare the participants for ASQ examination 24 PDU Certificate to maintain your PMI-CCR Get vital support- through email, online chat, telephone or webinar Six Sigma Green Belt: Six Sigma Green Belt, a popular business management strategy is widely used across industries towards quality and process improvement. This program empowers the participants the required tools and techniques to improve the quality of process outputs by identifying and removing the causes of defects (errors) and minimizing variability in manufacturing and business processes. Six Sigma Green Belt Certification Course benefits: To introduce the concept of Six Sigma To understand the tools and methods that are necessary to successfully participate in problem solving and DMAIC improvement projects in a manufacturing or transactional environment To learn the implementation of process mapping and measurement techniques in a particular organization To develop the knowledge and skills required to establish customer requirements and quantify process performance To get exposure to real life Six Sigma examples through case study analysis and discussion A scope to interact with Six Sigma expert from the industry and gain a comprehensive understanding of supporting an organization in implementing, managing and maintaining Six Sigma processes.   Contact us now: Kevin Johnson, Business Development Manager  Email id : kevin.john@courseraft.com Ph: +1 -201 -383 -5005  http://courseraft.com/course/operation
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Business Case Writing In Boston, Ma, United States
BostonJanuary 30, 2015 9:00 AM
Boston
Boston, MA 02108
Corporate strategy execution depends upon developing and implementing the best solution in the workplace. Success factors however, rely upon basing the solution on the right requirements, drawn from a sound and robust Business Case. A well crafted business case document outlines the rationale for undertaking a business project. It should be a formal, written argument that argues the reasoning to convince a decision maker to approve an intended action. A business case explores all feasible approaches to a given problem and enables business owners to select the option that best takes the organization forward. Its purpose is to define the parameters, risks and management factors involved within the project. It can be considered as a tool for the project manager to guide the design, management and evaluation of the project. A business case aims at capturing all the information, securing approval of human resources and finances required to successfully complete the project, and analysing risks and alternatives. Our one-day course packs in all the information you will need to create compelling business cases that are comprehensive and persuasive.   Benefits :  From the course : How to define the projectAnalyze, outline and communicate a business case effectively in writing to meet your requirementsIdentify and compare costs and advantages of alternative solutions to the problemThink of and apply risk assessment techniques to forecast and mitigate potential problemsBased on key decision criteria, work out alternative solutionsCommunicate and present the business case effectively to critical stakeholders to gain acceptanceFrom the workshop : High quality training from an industry expertEarn 8 PDUs / 8 CDUs from IIBAHard copy of the coursewarePractical hands-on exercises Faculty for Boston, MA (30th Jan 2015) Trainer details Certified PMP (Project Management Professional) with 14+ years experience as a Training Project Manager/ Head of IT/ ICT TrainerExcellent track record of applying best practices of project management and continuous improvement methodology in managing large training projects.A proven track record of significant improvements in learning processes, productivity & quality.Proficient in all aspects of Program Management, Training Need Analysis, Courseware Design, Corporate eLearning technologies, Educational Technology, Organizational Change Management, including full training project lifecycles.Excellent knowledge and skills in implementing cost effective training solutions using proven methodologies and project standards including but not limited to (ADDTIE, ISD, SCORM, SDLC/ASAP and PMBOK)
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In-person Seminar On Global Medical Device Regulations - Medical Devices
BostonJanuary 30, 2015 9:00 AM
Boston
Boston, MA 02108
Global Medical Device Regulations: US, EU, Canada, Argentina, Australia, Brazil, India, Japan, Mexico, Russia, South Korea, Taiwan: One and a Half-day In-person Seminar Location: Boston, MA Dates:JAN 29th 30th, 2015 Speaker:David Lim, Medical Device Dr. David Lim, Regulatory Doctor, obtained his Ph.D. in biological sciences at the University of Missouri-Columbia and published his thesis research in the prestigious journal Science. Since then, he has held various positions at Duke, Caltech, US National Laboratories, Intrexon Corporation, Terumo, US FDA/CDRH, and EraGen Biosciences (A Luminex Company). In 2009, Dr. Lim served as a panel member during the FDAs Transparency Public Meeting. Prior to founding his own consulting firm, www.RegulatoryDoctor.com, Dr. Lim was Senior Vice President of Scientific and Regulatory Affairs at Aquavit Pharmaceuticals. Regulatory Doctor provides Practical, Actionable and Sustainable/strategic Solutions in an Integrated, Thorough (PASS-IT) manner for all aspects of global regulatory, quality, clinical and compliance matters. Dr. Lim has analyzed over 1,000 FDA warning letters, attended more than 50 FDA Advisory Panel Meetings, and analyzed the subject matters and decision-making processes in detail. He is familiar with more than 200 medical devices, IVD products, biologics, drugs and combination products. Dr. Lim is a certified professional for regulatory affairs (RAC) and also is a certified quality auditor (CQA) by the American Society for Quality (ASQ). In addition, Dr. Lim has completed two years in law school. Dr. Lim is an auditor, regulatory coach, mentor, consultant and instructor for global matters pertaining to regulatory affairs, quality, clinical affairs and compliance. Course Description: Understanding global medical device regulations and requirement and adequate implementation of applicable medical device regulations can significantly expedite the regulatory processes, bringing innovative medical products to the global market faster and saving enormous amount of your unnecessary time, efforts and investment. At this workshop, you will get familiar with medical device regulations of twelve (12) countries concerning medical devices, active implantable medical devices and in vitro diagnostic medical devices for adequate implementation and successful registration. Reasons to attend: In this One and a Half-day In-person Seminar the trainer will walk you through to get familiar with the medical device regulations in the following twelve (12) countries. USEUCanadaArgentinaAustraliaBrazilIndiaJapanMexicoRussiaSouth KoreaTaiwanThis workshop is intended to provide guidance on medical device classification and registration requirements in these countries. The following areas will be discussed during the workshop: Medical device regulations in US, EU, Canada, Argentina, Australia, Brazil, India, Japan, Mexico, Russia, South Korea, TaiwanIn EU, the following four Directives will be discussed.DIRECTIVE 93/42/EEC Concerning Medical Devices (MDD)DIRECTIVE 90/385/EEC Concerning Active Implantable Medical Devices (AIMDD)DIRECTIVE 98/79/EC Concerning in vitro diagnostic medical devices (IVDD)DIRECTIVE 2007/47/EC Amending MDD and AIMDDISO 13485ISO 14155ISO 14971GHTF documentsMEDDEV guidance documentsClinical investigationAdverse event reportingTarget Audience: This seminar will be valuable for anyone in the European Commission (EC) and FDA-regulated industry, including, but not limited to, medical devices, active implantable medical devices, in vitro diagnostic medical devices or combination products. This seminar will be particularly useful for those involved in research and product development, handling data and documents for regulatory submission for CE-marking purposes, conducting/monitoring/coordinating clinical investigation, and/or performing risk management and post-market vigilance/surveillance. This workshop is a must for those who are directly or indirectly involved in drafting and handling applications for CE marking purposes. The following personnel will benefit from the course: Regulatory affairs (associates, specialists, managers, and directors)Quality assurance, quality control, and quality systems (associates, specialists, engineers, managers, directors and VPs)Research and development (associates, scientists, managers, directors and VPs)Product and development (associates, scientists, managers, directors and VPs)Contract research organization (associates, scientists, managers, directors and VPs)Site managers, and consultantsSenior and executive management (VPs, SVPs, Presidents and CEOs)Contractors and subcontractorsAnyone interested!AGENDA: Day 1: EU Directives 8:30am 9:00am - Registrations 9:00 AM 10:30 AM: Medical Device Regulations in US and Canada 10:30 AM 10:40 AM: Break 10:40 AM 12:00 Noon Medical Device Regulations in EUDIRECTIVE 93/42/EEC Concerning Medical Devices (MDD)DIRECTIVE 90/385/EEC Concerning Active Implantable Medical Devices (AIMDD)DIRECTIVE 98/79/EC Concerning in vitro diagnostic medical devices (IVDD)DIRECTIVE 2007/47/EC Amending MDD and AIMDD12:00 Noon 1:00 PM: Lunch 1:00 PM 2:30 PM Medical Device Regulations in Argentina, Australia, Brazil, India, and Japan 2:30 PM 2:40 PM: Break 2:40 PM 4:00 PM Medical Device Regulations in Mexico, Russia, South Korea, and Taiwan Day 2: GLP Workshop 8:30 AM 10:00 AM ISO 13485ISO 14971ISO 14155GHTF documents10:00 AM 10:10 AM: Break 10:10 AM 12:00 Noon MEDDEV guidance documentsClinical investigation   Please Click hear for Agenda. To Enroll for This Program Today please click hear Thank you & Regards, Kevin Roberts, Training Manager, kevin.roberts@complianzworld.com Call us at this Toll Free number: +1-866-978-0800 http://www.complianzworld.com
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The Boston Good Beer Passport: 1 Craft Beer At 20 Bars All Winter Long
BostonJanuary 30, 2015 10:00 AM
Boston
Boston, MA 02108
THE BOSTON WINTER GOOD BEER PASSPORT - 1 craft beer at each participating location for the whole winter January 15th through March 13th, 2015 Price: $35 Pintley and Burger Conquest are proud to present The Boston Winter Good Beer Passport! By purchasing a passport, you'll get one full craft beer at every one of the 20 participating locations. You can use them any day, any time from January 15th through March 13th, 2015. So grab your friends, brave the cold, and go on an adventure through the world of Boston's Craft Beer this winter! How it Works: Buy a ticket for the location where you would like to pick up your passport.Pick up your passport at the location you chose any day from January 15th through February 14th, 2015.Bring your passport to each of the 20 participating locations any day from January 15th through March 13th, 2015 and choose one full pour draft or bottled beer at each location.Valid only once per location.Please remember to tip your bartenders as gratuity is not included.Participating Locations: Blackstone GrillCape Ann Brewing CompanyChampions CambridgeChampions CopleyEast End GrilleFerry Street Food & DrinkHopstersKennedy's in the SquareLa Brasa - This location is not on the passport, please write it in on your passport when you pick it up. Located at: 124 Broadway, Somerville, MA 02145Menotomy Grill and Tavern Mystic StationNewburyport Brewing CompanyOlde Magoun's SaloonPatrons PJ RyansRiverwalk BrewingRoxy's Grilled CheeseSunset CantinaSunset's Grill and TapThe Vault  Fine Print: *Must be 21 years or older with valid ID *1 passport per person *You may buy 1 additional as a gift *Misplaced passports can not be replaced *Bars will choose which beers are available, many will have price limits of beers under $7 or $8 *Good Beer Passport is not valid at Pintley sponsored events Price: $35 About Pintley: Pintley is a craft beer community connecting drinkers, brewers, and bars. Drinkers use Pintley to discover great beer. Pintley learns from your tastes, suggests beers youll love, and invites you to free local beer tastings where you can try them. Brewers and bars use Pintley to grow. Pintleys craft beer events help bar managers fill their bars on slow nights, while helping breweries reach new audiences and accounts. About Burger Conquest: Burger Conquest is a blog written by sales marketing strategist, David Rev Ciancio about Hamburgers, travel and content marketing. Rev is the Director of Marketing at Burger Maker /Schweid & Sons, has been featured on numerous different TV shows and named an Expert Burger Taster by The Learning Channel. He is also the founder of The Burger Week, an annual delicious celebration of all things Burger in New York as well as South Florida and Charleston, SC. Bon voyage, Rachel
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Earn valuable points toward free nights.