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Robin B. Snyder

Director, Health Care Department

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Portrait of Robin B. Snyder

Robin is the Director of the firm's Health Care Department, and is responsible for the day-to-day operations and supervision of our health care attorneys. She is also a member of the firm's Board of Directors. From 2003 – 2017, Robin served as the Managing Attorney of the firm’s Moosic office.

Robin concentrates her practice in the defense of medical malpractice for physicians, nurses, hospitals, dentists and long term-care facilities. Her past litigation experience also includes defending school civil rights cases, which gives Robin a unique perspective in handling mental and behavioral health cases. Throughout her 29-year career with Marshall Dennehey, Robin has tried more than 40 cases to verdict, including medical malpractice and civil rights cases. As a seasoned litigator, Robin has served as a coach for the firm's Mock Trial program, providing guidance and mentorship to young attorneys as they hone their litigation skills.  

Following graduation from The Pennsylvania State University in 1987, Robin worked with the U.S. Securities and Exchange Commission and attended law school at Widener University School of Law in Wilmington, Delaware.

Robin is an elected associate member of the American Board of Trial Advocates (ABOTA), a national association of experienced trial lawyers and judges that works to enhance the civil trial jury system. She is admitted to the U.S. District Court for the Middle District of Pennsylvania and the Eastern District of Pennsylvania, as well as the Third Circuit Court of Appeals.

    • Widener University Delaware Law School (J.D., 1993)
    • The Pennsylvania State University (B.A., 1987)
    • Pennsylvania, 1993
    • U.S. District Court Eastern District of Pennsylvania
    • U.S. District Court Middle District of Pennsylvania
    • U.S. Court of Appeals 3rd Circuit
    • The Best Lawyers in America®, Litigation - Health Care (2023-2026)
    • American Board of Trial Advocates, 2022-present
    • Lackawanna County Bar Association - Board of Directors, 2016-2018; Civil Rules Committee, 2015-2018
    • Represented a hospital-based laboratory and its pathologists in an alleged misdiagnosis of breast cancer case. As a result of the diagnosis, which was interpreted as ductal carcinoma in situ, plaintiff underwent a lumpectomy and removal of lymph nodes resulting in mobility limitations and radiation which damaged her breast. A jury returned a verdict in favor of the laboratory and its pathologists. 
    • Obtained a defense verdict after a nine-day trial in Wayne County, Pennsylvania. The 52-year-old plaintiff presented to the emergency department with chest pain and stroke-like symptoms. She was administered 25 mg Phenergan IV in her hand, twice, and when her symptoms resolved and the MRI was clean, she was discharged. She returned two days later complaining of swelling in her hand and was diagnosed with infiltration. She claimed she developed Complex Regional Pain Syndrome and that she was disabled and unable to continuing working. Phenergan carries a Black Box warning that subcutaneous injection or perivascular extravasation may cause necrotic tissue. The jury found that the doctor, nurse and hospital did not breach the standard of care.
    • Tried a First Amendment political retaliation/freedom of association case in which she represented a school district. Plaintiffs alleged they suffered economic loss as a result of their political activities in supporting board members who ultimately lost the election. More significantly, plaintiffs alleged the retaliation occurred because they were friends with one another. Although we lost the case, after filing post-trial motions, the judge ordered a new trial, agreeing that his charge incorrectly implied that plaintiffs had a protected right of association for the purely social aspects of their relationships. We ultimately settled the case.
    • Successfully secured summary judgment in a case where plaintiff, a student at the University of Scranton/Wyoming Valley Healthcare System School of Nurse Anesthesia, was placed on academic probation and dismissed from the university. His complaint contained four causes of action, which were all dismissed: 1) breach of contract; 2) breach of the covenant of good faith and fair dealing; 3) denial of due process; and 4) tortious interference with contract. Plaintiff appealed, and the Third Circuit affirmed.
    • Involved in a major case involving alleged abuse of seven minor autistic students. Through their parents, they claimed they were assaulted by their teacher in violation of their constitutional rights, resulting in post-traumatic stress disorder. Represented the school district where the alleged abuse occurred and its administrators. Successfully had the 14th Amendment claim against the individuals dismissed. The school district had an indemnification clause in its contract with the entity that employed the teacher, and, ultimately, the case settled for multi-millions, none of which was paid by the school district.
    • Navigating Medical Malpractice: Insights into Pennsylvania’s Legal Landscape, Pennsylvania Chamber of Business and Industry Healthcare Summit, Harrisburg, PA, May 22, 2024
    • A Comparison of the Damages Awarded and Key Issues in Various Healthcare Jurisdictions, ILG360º London Annual Conference 2023, March 15, 2023
    • Business and Practice of Law Post-COVID-19: How Will It Change?, Pennsylvania Bar Association webinar, November 11, 2021
    • Civil Litigation Updates in COVID-19 Litigation – Where Do We Stand One Year Later?, Marshall Dennehey Webinar, May 2021
    • Telehealth and Documentation in the Time of COVID-19: Information and Best Practices to Protect Patients and Clinicians webinar, April 23 and May 14, 2020 

Thought Leadership

Legal Updates for Health Care Liability

Medical Malpractice Venue Rule Overturned

August 26, 2022

By Order dated August 25, 2022, effective January 1, 2023, the Supreme Court of Pennsylvania amended Pennsylvania’s venue rule, Pa.R.Civ.P. 1006, by deleting Rule 1006(a.1), which provided that medical malpractice actions must be filed “only in a county in which the cause of action arose.” Although this Rule change will not take effect until January 1, 2023, it will significantly change where many medical malpractice actions are filed. The effect of deleting Rule 1006(a.1) is to make medical malpractice actions subject to the same venue standards that apply to all other types of cases, which may be filed where (in relevant part) a defendant may be served, the cause of action arose, or a transaction or occurrence took place out of which the cause of action arose. Yesterday's Rule change will significantly expand the counties in which medical malpractice actions may be filed, with an expected increase in certain counties, primarily Philadelphia. This change eliminates a centerpiece of the Supreme Court’s own tort reform effort 20 years ago. By Order dated January 27, 2003, the Court promulgated Rule 1006(a.1) requiring medical malpractice actions to be filed only where the cause of action accrued. The result was a significant decline in medical malpractice filings statewide. The Order accompanying the Rule change states: “This Order shall be processed in accordance Pa.R.J.A. 103(b), and shall be effective January 1, 2023.” This language likely means that the amendment to Rule 1006 will apply to actions filed on or after January 1, 2023, regardless of when the cause of action accrued. When the Supreme Court promulgated Rule 1006(a.1) in 2003, the effective date applied to filings, and this Rule change likely will apply the same way. When Rule 1006(a.1) was promulgated in 2003, many plaintiffs rushed to file their medical malpractice actions before the Rule change took effect. We will likely now see the reverse trend: plaintiffs will wait until on or after January 1, 2023, to file new actions in venues that they view as more favorable. Finally, in addition to Rule 1006(a.1), there is a statute—42 Pa.C.S.A. § 5101.1(b)—that requires medical malpractice actions to be filed where the cause of action arose. However, that statute was declared unconstitutional in North-Central Pennsylvania Trial Lawyers v. Weaver, 827 A.2d 550 (Pa. Cmwlth. 2003), on the basis that venue is a matter for the Supreme Court, not the legislature. Yesterday’s Order suspends any statute that is inconsistent with Rule 1006 as amended, so it is likely that the amended Rule, not the statute, will govern venue in medical malpractice cases beginning on January 1, 2023.   Legal Update for Health Care Liability - August 26, 2022, has been prepared for our readers by Marshall Dennehey. It is solely intended to provide information on recent legal developments,and is not intended to provide legal advice for a specific situation or to create an attorney-client relationship. We welcome the opportunity to provide such legal assistance as you require on this and other subjects. If you receive the alerts in error, please send a note to tamontemuro@mdwcg.com. ATTORNEY ADVERTISING pursuant to New York RPC 7.1. © 2022 Marshall Dennehey. All Rights Reserved.

Firm Highlights

Result

No-Cause Jury Verdict Secured in Wrongful Death Trial

We successfully obtained a no-cause jury verdict in a 13-day wrongful death trial. The decedent, a 59-year-old man, was admitted to the emergency room on February 15, 2019, with complaints of abdominal pain, decreased appetite, and constipation, despite the use of laxatives. The patient did not complain of any nausea, vomiting, or diarrhea. He had a significant medical history including diabetes, hypertension, prior coronary artery stenting, morbid obesity (with past gastric bypass surgery), longstanding ventral hernia, and back pain. A CT scan revealed multiple hernias and a potential closed-loop bowel obstruction, leading to a surgery consultation. Our client, an emergency general surgeon, interpreted that the patient did not have a closed loop or any significant obstruction and recommended non-surgical management. The patient was approved to have clear liquids, and had a vomiting incident shortly after, but our client was not notified. The patient was returned to NPO status, and after improving overnight, he was returned to “clears” and additional medical and renal consults were ordered. Our client did not receive any communications from the residents/nurses of any changes in the patient’s condition. On February 18, 2019, two rapid responses were called due to increased heart rate and vomiting. It is believed that the vomiting resulted in aspiration, causing sepsis, ultimately leading to the patient’s death. During the trial, the plaintiff’s sole medical expert highlighted imaging on the wrong hernia, which called into question all of his opinions in the case. We made key objections related to the expert testimony, limiting what the allegations were, and preventing new allegations from being made. After approximately two and a half hours of deliberating, the jury returned a no-cause verdict. 

Thought Leadership

SIDEBAR: News and Happenings

We are pleased to share that attorneys from our health care team have been selected to the 2026  New Jersey and Pennsylvania Super Lawyers and Rising Stars lists. Their dedication to clients and commitment to high-quality work continues to strengthen our firm! Please join us in congratulating: NJ Super Lawyers: Robert T. Evers and Justin F. Johnson NJ Super Lawyer Rising Stars: Nataliana A. Guida  2026 Pennsylvania Super Lawyers: Alyson J. Kirleis and Gary M. Samms 2026 Pennsylvania Rising Stars: Holli K. Archer and Daniel Dolente Victoria Scanlon (Scranton) was a faculty presenter at the 2026 American Roentgen Ray Society (ARRS) Annual Meeting in Pittsburgh. She participated in the “Resident Symposium: Producing Quality Reports,” focusing her presentation on “How to Write a Great Report: Malpractice Lawyer’s Perspective.” Vicky, the only attorney presenter for this two-hour segment, was joined by several health care professionals including diagnostic radiologists, an interventional radiologist, an internal medicine physician, and a radiologist turned AI entrepreneur expert.  Matthew Keris (Scranton), President of the Pennsylvania Association for Health Care Risk Management (PAHCRM) and shareholder in our Scranton Health Care Department, presented an important and timely session titled “Keynote Address: A Conversation with RaDonda Vaught on Criminalizing Errors” at PAHCRM’s Annual Meeting in April. RaDonda is a former Tennessee nurse widely known for being criminally convicted in 2022 of negligent homicide and gross neglect after a 2017 fatal medication error at Vanderbilt University Medical Center. Her case gained national attention because she was criminally prosecuted rather than just facing licensing board action, sparking debate over blaming individual nurses for systemic healthcare failures. Matt and RaDonda’s conversation explored one of the most consequential issues in health care risk management today—how systems respond to human error, and what it means for patient safety, accountability, and the professionals who serve on the front lines. Gary Samms was a panelist for a podcast hosted by the Medical Liability Monitor, “From Outliers to Pattern: The Increasing Predictability of Megaverdicts in the Med-Mal Industry – and How to Reduce the Likelihood of Getting Hit with One.” Gary discussed the changing megaverdict landscape and why “outlier” verdicts are becoming structural, in addition to how plaintiffs turn weaknesses into megaverdicts (including building emotional narrative and jury psychology). Thank you to our clients who joined us for our Trends in Health Care & Health Law seminar on May 14. Led by our Health Care Department Director and Assistant Director, Robin Snyder and Donna Modestine, the session explored key issues that are currently shaping outcomes in health care litigation. We owe a debt of gratitude to our esteemed guest speaker, Mary Ellen Nepps, Esq., Senior Counsel, University of Pennsylvania, who presented “Medical Malpractice Litigation: Driving Another Health Care Crisis in Pennsylvania.” And special thanks to our attorneys who presented and shared their insights, including John J. Hare and Holli Archer who discussed “Highlights in PA Medical Malpractice Law;” David Drake for his presentation, “From Claims to Courtroom: Key Trends in NJ Medical Malpractice Litigation;” and Matthew Keris with an “Update on Health Care Tech Discovery.” Thank you to all of our clients for entrusting us with your health care litigation. We are proud to partner with you as we defend your interests and navigate legal landscapes together.

Thought Leadership

Casual Care, Serious Consequences: How Informal Prescribing Can Trigger Medical Board Scrutiny

The lesson for health care practitioners is that regular review of the regulatory requirements can ensure compliance and that casual prescribing may be in violation of state regulations if the necessary components are not met. Consider the following scenario: in December 2025, a medical provider renewed a prescription for a long-standing telemedicine patient receiving a Schedule II controlled dangerous substance. This was not a violation of the New Jersey Administrative Code. Another provider doing the same action for an equally situated patient in March 2026 would be in violation. The casual prescriber who is not aware of newer regulatory requirements may have a more difficult time responding to a medical board complaint. Medicine is a highly-regulated helping profession. Without addressing the merits of this regulatory burden, the practice of medicine continues to see drastic changes impacting the everyday life of patient and provider. Telemedicine, COVID-19, and other advances and roadblocks, present a challenge to those saving lives while attempting to comply with the rules of practice. Physicians often discover—through real cases and the lens of regulatory expectations—that even well-intentioned informal help can be reinterpreted as stepping outside mandated professional boundaries, and seemingly harmless actions can be construed as deviations from required practice standards specifically outlined in Title 13, Chapter 35, Subchapters 7.1A of the New Jersey Administrative Code. Title 45, "Professions and Occupations," of the New Jersey code governs the practice of medicine, nursing, optometry, pharmacy, and many other professional occupations. Section 9 specifically addresses the state board of medical examiners and allows for the creation of rules and regulations in Section 45:9-5.3. These regulations can be found in the New Jersey Administrative Code Title 13, Chapter 35. While broad in scope, Chapter 35 contains a subchapter dedicated to the administration and dispensing of prescription drugs. Such knowledge will arm physicians with the tools they need to prevent a negative outcome if a medical board complaint is filed. Likewise, attorneys must be familiar with these regulatory requirements when advising and defending providers. In New Jersey, N.J.A.C. Section 13:35-7.1A(a) requires that a practitioner conduct an examination and appropriately document the same within the medical record before dispensing drugs or issuing prescriptions. The examination must include an "appropriate history and physical examination," a diagnosis based upon the examination and any testing consistent with good medical care, the formulation of a therapeutic plan discussed with the patient, and the availability of appropriate follow-up care. There are only six exceptions to this requirement: In admission orders for a newly hospitalized patient For a patient of another physician for whom the practitioner is taking calls For continuation medications on a short-term basis for a new patient prior to the patient's first appointment For an established patient who, based on sound medical practice, the physician believes does not require a new examination before issuing a new prescription For a patient examined by a healthcare professional who is in collaborative practice with the practitioner When treatment is provided by a practitioner for an emergency medical condition Emergencies are also limited to situations where someone's health is in serious jeopardy, there is serious impairment to bodily functions, or serious dysfunction of any bodily organ or part. During the COVID-19 pandemic, then New Jersey Governor Phil Murphy issued an executive order declaring a public health emergency and a state of emergency that allowed authorized prescribers to prescribe Schedule II controlled dangerous substances via telemedicine. The order was terminated when he left office earlier this year and the state reverted to the requirement of an initial in-person examination and quarterly in-person visits. With this return to prior regulatory requirements, practitioners subject to the jurisdiction of the board of medical examiners may benefit from a refresher on the regulatory limitations on their practice now that the pandemic-era flexibilities have ended. This new requirement may create confusion for prescribers and lead to casual prescribing of medication in violation of the regulations, even in the setting of recurrent telemedicine appointments as noted in the example above. Casual prescribing can take many forms: filling a prescription request from a friend or family member without an examination or contemporary medical record; using telemedicine to expand your practice without proper in-person appointments or documentation in the medical record; failing to ensure appropriate follow-up care for a "one time" prescription; etc. Although not all board complaints end in a publicly available opinion, serious deviations from regulatory requirements can shine a light on practices that will require action by the board if a complaint is received. Consider the following cases: In October 2025, the board issued a final consent order in an administrative action where a doctor provided opioids without examination and his license was permanently revoked. In re Robert Dela Gente, D.O., N.J. State Bd. of Med. Exam'rs Oct. 21, 2025. Criminal charges were filed (though that is not always the case). In a September 2025 consent order, a physician was reprimanded for "prescribing opioids several months in advance without the proper patient follow-up..." and explained that they did so for "patients who can not pay for multiple visits to refill medications." In re A/an E. Schultz, M.D., N.J. State Bd. of Med. Exam'rs Sept. 25, 2025. Another physician was suspended and placed on probation in a consent order for prescribing three patients the weight-loss medication "Ozempic" via text messages through a website called "Push Health" and without any further communication with the patients or taking a medical history. In re Laura E. Purdy, M.D., N.J. State Bd. of Med. Exam'rs Aug. 29, 2025. A June 2025 interim consent order required a "full evaluation and assessment of [a physician's] general knowledge and skill, with specific emphasis on his knowledge of and ability to safely prescribe [controlled dangerous substances]" due to his failure to review a patient's prior medical history and medical record, assess and review the prescription monitoring program before prescribing CDS, and conduct random urine screens on a patient that tested positive for CDS upon admission to his practice because "he trusted the patient." In re Donald Oh, M.D., N.J. State Bd. of Med. Exam'rs June 2, 2025. Each of these examples demonstrate a failure to follow strict procedure regardless of the intention. Failing to follow procedure secondary to good intentions, such as considering a patient's financial constraints, trust in the patient, or utilizing a new telemedicine service platform, will not be a defense to a board complaint. Especially when practicing via telemedicine, practitioners must ensure they are adhering to the appropriate regulatory standard. A provider who calls in a prescription for a traveling friend or family member or agrees to prescribe medication for individuals using the newest phone app will have a hard time meeting the requirements of N.J.A.C. Section 13:35-7.1A. Even if a history was taken, a "therapeutic plan" was created, and "follow up care" was provided, the prescriber would still not be in compliance with the regulation without an in-person examination. In our opening hypothetical, the prescriber's behavior did not change between December and March; however, the legal shift in the regulatory landscape made once acceptable behavior a violation as a required examination did not occur. When complaints are made with regard to informal prescribing, the board has discretion to employ measures to encourage compliance in lieu of formal proceedings such as a private, written warning; suspending fines subject to continuing compliance; medical or professional treatment as may be necessary; medical or diagnostic testing and monitoring; skills assessment; corrective training; participation in outreach programming; or contribution to the consumer fraud protection fund. The lesson for health care practitioners is that regular review of the regulatory requirements can ensure compliance and that casual prescribing may be in violation of state regulations if the necessary components are not met. Even compliant providers who had not conducted an in-person examination for telemedicine patients during the COVID-19 emergency would be in violation of the regulations as of January 2026 for the same practice. Practitioners should be diligent in adhering to the prescribing rules to avoid sanctions related to casual care. Likewise, attorneys advising or defending practitioners before the board must be aware of the in-person examination requirements for prescribing in New Jersey whether the care in question took place in-person or in a telemedicine setting. Reprinted with permission from the April 22, 2026 issue of the New Jersey Law Journal. ©2026 ALM Media Properties, LLC. Further duplication without permission is prohibited. All rights reserved.