Medmarc Insurance Group

Medmarc's mission to serve the medical technology and life sciences industry remains unchanged since our inception in 1979.

Medmarc is the one-stop-shop for insurance solutions for manufacturers and distributors of medical technology and life sciences products.

Mission: Medmarc’s mission is to be the superior provider of liability insurance protection and related risk management solutions to the medical technology and life sciences industry.

Medmarc Insurance Group

Medmarc Insurance Group

In observance of Thanksgiving, our offices will be closed from Thursday, November 28th through Sunday, December 1st. We will resume normal business hours on Monday, December 2nd.

Please take the time this weekend to remember the sacrifices our military men and women have made for this country. #memorialday2019

Medmarc sponsored a Dulles South Food Pantry packing event at our new office space on May 2, 2019. Because of Medmarc and our gernerous employee contributions, we were able to donate 1055 lbs. of food and pack 206 Friday food packs!

Check out how we did it on our YouTube Channel. https://youtu.be/Mbe2It347AA

Medmarc New Office Location - April 1, 2019

Join Medmarc’s Risk Management Department on Wednesday in a webinar that breaks down some of the biggest headlines from the last year and discuss what life sciences companies can take away from these stories and what they should have their eyes on in 2019.

Register today: https://www.medmarc.com/news-and-resources/webinars/webinar-details/?webinar=2342&requestPath=/news-and-resources/

Profile Pictures

youtube.com

Medmarc Risk Management Mission

Sara Dyson, Assistant Vice President Risk Management, Medmarc Insurance Group, discusses the services Medmarc provides and how they are designed to prevent and mitigate products liability risks in this video. https://www.youtube.com/watch?v=eY_AXSaU5JE&feature=youtu.be

Sara Dyson, Esq., Medmarc’s Assistant Vice President of Risk Management, discusses the services Medmarc provides and how they are designed to prevent and mit...

Medmarc - Insurance for the Life Sciences and Medical Device Industry | Announcement Details

Medmarc is pleased to announce that A. M. Best upgraded all Medmarc Companies to A+. Go to Https://www.medmarc.com/news-and-resources/announcements/announcement-details/?announcement=1898&requestPath=/announcements for more information.

medmarc.com CHANTILLY, VA and BIRMINGHAM, AL., August 23, 2017– Medmarc Casualty Insurance Company (Medmarc) and Noetic Specialty Insurance Company (Noetic) have been upgraded to A+ (Superior) by A. M. Best.

Medmarc Insurance Group

Medmarc Insurance Group's cover photo

Come visit booth #904 ProAssurance & Medmarc at ASHRM 2016 to learn more about our single source for innovative healthcare liability insurance solutions #ashrm2016

http://www.ashrm.org/annual-conference/

Medmarc Insurance on Twitter

Twitter Poll - We Want to Hear From You
https://twitter.com/MedmarcIns/status/730028947107291136

twitter.com “What technology do you think will have the greatest impact on the future of healthcare?”

Senior Claims Examiner Jobs in Chantilly, VA - Medmarc

We are hiring a Senior Claims Examiner in our Medmarc (Chantilly VA office) to join our team! http://www.careerbuilder.com/jobseeker/jobs/jobdetails.aspx?job_did=JHT08H6C3Z5FL03FBXC&siteid=cbnsv&showNewJDP=yes&ipath=JRG2

careerbuilder.com Apply Now Senior Claims Examiner Medmarc Chantilly, VA 4/15/2016 Save Job Sign in Now Email Report 1 Applications Submitted for this Position See education levels, salary, and years of experience. With our competition report, only with a Careerbuilder account. Create Account Job Description Medmarc,…

www.medmarc.com

ProAssurance Announces Life Sciences Leadership Changes at Medmarc Insurance http://bit.ly/1PGiJI7

medmarc.com

careerbuilder.com

Desktop Engineer II Jobs in Chantilly, VA - Medmarc Insurance Group

We are seeking a highly motivated Desktop Engineer II in our Medmarc (Chantilly VA office) to join our team!

A Desktop Engineer II is to serve as the first point of escalation for the tier 1 technician and to serve as a resource for Business Project and Internal IT Projects. This position will work closely with the Security, Network, Desktop and Systems Engineers to accomplish improvements to systems, processes, and customer experiences.

For more details, check out the job description on Career Builder. http://cb.com/1MCVfRJ

careerbuilder.com Apply Now Desktop Engineer II Medmarc Insurance Group Chantilly, VA 11/6/2015 Save Job Sign in Now Email Report Job Description Medmarc is the leading expert in medical technology and life sciences products liability insurance, and is part of ProAssurance, a leading health-centric specialty insuranc…

medmarc.com

ProAssurance Announces the Upcoming Retirement of Mary Todd Peterson

ProAssurance Announces the Upcoming Retirement of Mary Todd Peterson, President of Medmarc Insurance Group

medmarc.com BIRMINGHAM, Ala., Sept. 16, 2015 /PRNewswire/ -- ProAssurance Corporation (NYSE: PRA) announced today that Mary Todd Peterson, the President of the Medmarc Insurance Group (Medmarc), will retire effective December 31, 2015. Medmarc is ProAssurance's subsidiary providing products liability insurance…

Stay up to date with Medmarc by following us on Twitter. You will also be entered in for a chance to win. https://twitter.com/MedmarcIns

Recalls & Life Sciences Companies: A Guide to Effective Preparation and Execution

http://www.medmarc.com/Life-Sciences-News-and-Resources/Webinars/Pages/Recalls-and-Life-Sciences.aspx?utm_source=facebook&utm_medium=webinar&utm_campaign=recalls

medmarc.com Recalls are increasingly common in the drug and medical device industry. Though always unwelcome, they are events for which every life sciences company should prepare. Many companies have recall plans in place, but there are some common components of such plans that are frequently overlooked at pote…

Medmarc Insurance Group's cover photo

blogs.fda.gov

Innovative New Drugs Are Reaching Patients at a Fairly Constant Rate: New FDA Study Reports on...

FDA: http://blogs.fda.gov/fdavoice/index.php/2013/08/innovative-new-drugs-are-reaching-patients-at-a-fairly-constant-rate-new-fda-study-reports-on-25-year-record-of-approvals/

blogs.fda.gov Innovative New Drugs Are Reaching Patients at a Fairly Constant Rate: New FDA Study Reports on 25-year record of approvalsPosted on August 5, 2013 by FDA VoiceBy: Mike LanthierSo much has been said and written about the supposed innovation gap in drug discovery that it’s generally been accepted as t...

imarcresearch.com

3 Costly Traps on the Road to Device Innovation

http://www.imarcresearch.com/blog/bid/304870/3-Costly-Traps-on-the-Road-to-Device-Innovation

imarcresearch.com No matter the therapeutic area, device companies agree: Creating cutting-edge products is expensive.

fdalawyersblog.com

Facility Inspection Guidance Issued by FDA: Delaying, Denying, Limiting, or Refusing a Drug...

http://www.fdalawyersblog.com/2013/07/facility-inspection-guidance-i.html

fdalawyersblog.com On July 12, 2013 FDA issued new Guidance for Industry: Circumstances that Constitute Delaying, Denying, Limiting, or Refusing a Drug Inspection. The Guidance document illustrates circumstances where the FDA will treat the occurrence as contrary to section 501(j). These are... Published By Frommer La...

Mike Garofalo Joins Medmarc as Director of Strategic Markets

https://www.medmarc.com/Life-Sciences-News-and-Resources/Announcements-and-Events/Pages/Mike-Garofalo-Joins-Medmarc.aspx

medmarc.com Inquiries regarding Medmarc should be directed to George Ayd, Assistant Vice President at (800)-356-6886, ext. 309. Please contact your current broker for additional information regarding what Medmarc can do for you.

medcitynews.com

Report says mHealth sensor market will grow 70% annually -- but what about slow adoption?

http://medcitynews.com/2013/04/report-says-mhealth-sensor-market-will-grow-70-annually-but-what-about-slow-adoption/

medcitynews.com Last week I read and wrote about a physician survey which suggested that few people are using mobile health apps to track data and share it with their doctors (although a reader noted that the Pew data I referenced likely underestimates the self-tracking that’s really going on).

medcitynews.com

FDA finds violations at 28 drug compounding pharmacies

http://medcitynews.com/2013/04/fda-finds-violations-at-28-drug-compounding-pharmacies/

medcitynews.com The FDA has found safety violations at 28 of 29 compounding pharmacies that are supposed to be producing sterile drugs. In other news, a drug patent on OxyContin expires this week, but generic versions could take a while to produce. Medpage Today: FDA Turns Up Heat On CompoundersFDA inspectors issue...

medcitynews.com

Top five tips for successfully addressing warning letters

http://goo.gl/iMBSk

medcitynews.com Each year, the FDA issues hundreds of warning letters to medical device companies for reasons ranging from manufacturing practice violations to breaches in labeling and misbranding. Companies responding well to the FDA’s demand for prompt compliance will ultimately return to the agency’s good grac...

businessweek.com

House Republicans Question FDA on Mobile Medical Software: Taxes

http://www.businessweek.com/news/2013-03-15/house-republicans-question-fda-on-mobile-medical-software-taxes

businessweek.com Republicans in Congress are probing whether the president’s health-care overhaul will mean higher taxes for companies that sell mobile medical applications.

businessweek.com

House Republicans Question FDA on Mobile Medical Software: Taxes

http://www.businessweek.com/news/2013-03-15/house-republicans-question-fda-on-mobile-medical-software-taxes

businessweek.com Republicans in Congress are probing whether the president’s health-care overhaul will mean higher taxes for companies that sell mobile medical applications.

U.S. health care spending topped $1.2 trillion in 2010 : Internal Medicine News

http://www.internalmedicinenews.com/index.php?id=514&tx_ttnews%5Btt_news%5D=141481&cHash=1a48abcb216b53c356f76a7e12257f82

internalmedicinenews.com The total cost of health care in the United States was $1.26 trillion in 2010, according to a report from the Agency for Healthcare Research and Quality. Hospital inpatient costs accounted for the largest share (31%) of the total, which applies to the civilian, noninstitutionalized population. Ambu...

medicaldevicesummit.com

Medical Device Tax: Impact on Manufacturers and Importers | News | Medical Device Summit

http://www.medicaldevicesummit.com/Main/News/51011b2c-9bd1-452f-86d6-4df0f82ca2ed.aspx

medicaldevicesummit.com This article presents a brief overview of the medical device tax, which products it affects and when payments are due.

FDA to Release Long-Awaited Guidance on CMO Agreements, Biosimilars in 2013

http://www.in-pharmatechnologist.com/Regulatory-Safety/FDA-to-Release-Long-Awaited-Guidance-on-CMO-Agreements-Biosimilars-in-2013?utm_source=RSS_text_news&utm_medium=RSS%2Bfeed&utm_campaign=RSS%2BText%2BNews

in-pharmatechnologist.com Highly sought-after guidance on quality agreements for contract manufacturing organizations (CMOs) and biosimilar developers is expected in 2013, according to a list of future guidance documents released by the US Food and Drug Administration (FDA).

Litigation for Life Science Companies: Aspects of Litigation That Should Affect How You Run Your Bus

http://www.medmarc.com/Life-Sciences-News-and-Resources/Products-Liability-360-Newsletter/Pages/Litigation-for-Life-Science-Companies.aspx

medmarc.com This last article will focus on aspects of the litigation process that companies should be aware of that could affect how they develop and market medical devices in the future.

Medmarc® Blog - FDA Issues Final Rule on Combination Products

FDA Issues Final Rule on Combination Products. http://blog.medmarc.com/archive/2013/01/28/fda-issues-final-rule-on-combination-products.aspx

blog.medmarc.com FDA is charged with regulating a wide swath of products we use every day, and whether foods, drugs, cosmetics, medical devices, biologics, or otherwise, FDA applies a specific set of regulations tailored to the particular product category. However, sometimes the categories overlap, for example, in t...

imarcresearch.com

Is the Medical Device Review Process Improving?

http://www.imarcresearch.com/blog/bid/263137/Is-the-Medical-Device-Review-Process-Improving

imarcresearch.com Could this coming year be the start of a new relationship between FDA and medical device industry?

FDA Law Blog: FDA Issues Final Rule on CGMP Requirements for Combination Products; Requirements for.

FDA Issues Final Rule on Combination Products:
http://www.fdalawblog.net/fda_law_blog_hyman_phelps/2013/01/fda-issues-final-rule-on-cgmp-requirements-for-combination-products-requirements-for-convenience-kit.html

fdalawblog.net By Carmelina G. Allis – The FDA has issued a final rule on the current good manufacturing practice (CGMP) requirements applicable to combination products. 78 Fed. Reg. 4307 (Jan. 22, 2013). This rule finalizes a proposed rule issued on September...

medicaldevicesummit.com

Medical Device Supply Chain Summit | Events | Medical Device Summit

Medmarc's Sara Dyson will be speaking on products liability risk in the supply chain at tomorrow's Medical Device Supply Chain Summit in Washington, DC. http://medicaldevicesummit.com/Main/Events/Medical-Device-Supply-Chain-Summit-111.aspx

medicaldevicesummit.com This annual summit brings together senior industry experts to discuss strategies and best practices for managing risk and increasing quality and efficiency in the medical technology supply chain. January 24 - 25, 2013. Marriott Wardman Park Hotel, Washington, DC  Attend On-site or Off-site...

FDA Publishes 2013 Fiscal Year Guidance Document Schedule | Aptiv Solutions

FDA releases schedule of Guidance Documents it plans to publish this year.
http://www.aptivsolutions.com/blog/medical-device/2013/01/fda-publishes-2013-fiscal-year-guidance-document-schedule/

aptivsolutions.com The CDRH has put together a list of the medial device guidance documents that it is proposing to publish throughout the 2013 fiscal year.

medcitynews.com

Europe Ups the Post-Market Ante for New Medical Devices

http://medcitynews.com/2013/01/europe-ups-the-post-market-ante-for-new-medical-devices/

medcitynews.com While Europe may still provide a faster route to regulatory approval for such devices, post-market requirements are creeping in like an expensive final cheese course served by European regulators and health systems just when companies are feeling most broke and tired. So regulatory approvals may com...

fdalawyersblog.com

Safety Reporting Requirements Explained -- More Targeted Reporting Emphasized - FDA Lawyers Blog

http://www.fdalawyersblog.com/2013/01/safety-reporting-requirements.html?utm_source=feedburner&utm_medium=feed&utm_campaign=Feed%3A+FdaLawyersBlogCom+%28FDA+Lawyers+Blog%29&utm_content=Google+Reader

fdalawyersblog.com Towards the end of last year, FDA added two new final guidances related to the safety reporting requirements for investigational new drug exemptions ("INDs") and bioavailability and bioequivalence ("BA/BE") studies entitled: Guidance for Industry and Investigators: Safety Reporting Requirements for....

medcitynews.com

Five innovations that will define tech in 2013, including an FDA battle over digital health

Medmarc [email protected]

Five innovations that will define tech in 2013, including an FDA battle over digital health - http://goo.gl/t6QTZ

medcitynews.com What lies ahead for 2013? An intense battle with the FDA over big data and digital health, new user interfaces, and Google Now are three things to expect.

mobihealthnews.com

Pew: 35 percent of US adults are online diagnosers | mobihealthnews

http://goo.gl/vc7v0

mobihealthnews.com When it comes to looking for health information online, consumers have had fairly consistent behaviors over the past 12 years. A new report, Online Health 2013, from The Pew Research Center’s Internet & American Life Project found that of the 81 percent of US adults who use the internet, 72 percent ...

medmarc.com

A.M. Best to Review Medmarc's Rating Given Merger with ProAssurance

https://www.medmarc.com/Life-Sciences-News-and-Resources/Announcements-and-Events/Pages/AM-Best-Press-Release-on-Merger%27s-Rating-Implications.aspx

medmarc.com Medmarc announced yesterday that it is to become part of ProAssurance, a $5-billion dollar organization with an A.M. Best rating of "A." Shortly thereafter, A.M. Best issued a Press Release on the likely effect of this merger on Medmarc's own rating, stating. "A.M. Best Co. has placed under review w...

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14280 Park Meadow Dr Ste 300
Chantilly, VA
20151

Opening Hours

Monday 08:30 - 17:00
Tuesday 08:30 - 17:00
Wednesday 08:30 - 17:00
Thursday 08:30 - 17:00
Friday 08:30 - 17:00
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