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.

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:

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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.

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:// for more information. 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

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

Medmarc Insurance on Twitter

Twitter Poll - We Want to Hear From You “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! 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,…

ProAssurance Announces Life Sciences Leadership Changes at Medmarc Insurance

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. 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…

ProAssurance Announces the Upcoming Retirement of Mary Todd Peterson

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

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

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

FDA: 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...

3 Costly Traps on the Road to Device Innovation No matter the therapeutic area, device companies agree: Creating cutting-edge products is expensive.

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

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

FDA finds violations at 28 drug compounding pharmacies 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...

Top five tips for successfully addressing warning letters 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...

House Republicans Question FDA on Mobile Medical Software: Taxes Republicans in Congress are probing whether the president’s health-care overhaul will mean higher taxes for companies that sell mobile medical applications.

House Republicans Question FDA on Mobile Medical Software: Taxes 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 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...

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

Is the Medical Device Review Process Improving? 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: 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...

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

Europe Ups the Post-Market Ante for New Medical Devices 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...

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

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

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

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

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

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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