Federal Regulation Lawyer in ZIP Code 98101 - Seattle

Location: 98101, Seattle, Washington
Phone: Not Available
Firm: Feldman Law Firm, PLLC

Legal counsel, advocacy, and regulatory advice.

Location: 20007, Washington, District Of Columbia
Phone: +1 (202) 902-9392
Firm: GKG Law, PC

Location: 20007, Washington, District Of Columbia
Phone: Not Available
Firm: Ubias Law PLLC

I am Managing Partner at Ubias Law, PLLC.  I advise emerging and growth companies with an international footprint on compliance with trade and investment activities subject to US laws.  I counsel small business seeking federal government contracts and advise on compliance requirements.   I also counsel and collaborate with companies working with distributed ledger technology, cryptocurrencies and digital asset management blockchain solutions to navigate the patchwork of regulations and evolving guidance from the regulators and the requirements of evolving legislation. My practice also includes advising public and private companies in navigating compliance and due diligence issues in capital market transactions and e-discovery consulting and subpoena responses.

Location: 20007, Washington, District Of Columbia
Phone: Not Available
Firm: Stagg PLLC

Location: 20007, Washington, District Of Columbia
Phone: Not Available
Firm: Foley & Lardner LLP

David Rosen is a partner and public policy lawyer with Foley & Lardner LLP. Mr. Rosen has extensive experience in health law, life sciences, and food and drug regulation, including a range of Food and Drug Administration (FDA) regulatory issues affecting prescription and over-the-counter pharmaceuticals, medical devices and biologics. He is co-chair of the firm’s Life Sciences Industry Team and is also a member of the firm’s Government & Public Policy Practice and the Health Care and Food & Beverage Industry Teams.. Mr. Rosen was formerly a partner with two other law firms. He was also employed by the FDA for 14 years, progressing to various supervisory positions involving virtually all aspects related to the drug approval process, combination products, jurisdictional issues and related compliance activities.. Recognition. Mr. Rosen has been Peer Review Rated as AV® Preeminent™, the highest performance rating in Martindale-Hubbell's peer review rating system. In 2012 - 2015, The Legal 500 recognized Mr. Rosen for his work in life sciences. In 2015, he was named an IP Star by Managing Intellectual Property magazine. He has been a frequent speaker before national and international pharmaceutical industry associations on the ANDA submission and review process and on the IND and expedited drug development, review, and approval processes. Mr. Rosen has made presentations before investment analysts and managers of venture capital on the impact of FDA on the drug and biotech industry.. Affiliations. Mr. Rosen is a member of the University of Connecticut School of Pharmacy Advisory Board.. Education. Mr. Rosen earned his J.D. at The Catholic University of America, Columbus School of Law (1991). He also holds a Bachelor of Science degree from the University of Connecticut School of Pharmacy (1978).. Admissions. Mr. Rosen is admitted to practice in the District of Columbia and Maryland.. Publications

Location: 20008, Washington, District Of Columbia
Phone: Not Available

Location: 20036, Washington, District Of Columbia
Phone: Not Available
Firm: Berliner, Corcoran & Rowe, Llp

Location: 20036, Washington, District Of Columbia
Phone: Not Available
Firm: Mcfadden & Shoreman

Location: 20036, Washington, District Of Columbia
Phone: Not Available
Firm: Hudson Cook, LLP

Location: 20036, Washington, District Of Columbia
Phone: Not Available
Firm: SCHIFF HARDIN LLP

Location: 20037, Washington, District Of Columbia
Phone: Not Available
Firm: Olsson, Frank Weeda Terman Matz P.C.

Evan Phelps is a principal at OFW Law. He advises companies on compliance with Food and Drug Administration (FDA) law and regulations, with focus on matters related to medical devices and biologics as well as those affecting Clinical Investigators. This includes Assistance in the preparation of Premarket Approval Applications (PMAs), Premarket Notifications (510(k)s), and Investigational Device Exemption (IDE) Applications; Advice, training, and assistance with matters concerning the Quality System Regulation (QSR) and the Medical Device Reporting (MDR) Regulation; Assistance with responding to and resolving issues relating to: FDA establishment inspections, Forms FDA-483 (Inspectional Observations), Warning Letters, Recalls, Injunctions, Import/Export of FDA-regulated products, and Product labeling. Evan also assists in Clinical Investigators and IRBs with compliance, enforcement, and training issues. He advises companies on the impact of FDA law on business transactions and agreements; development of specially tailored plans to bring medical devices to market based upon client needs and goals; and assists in filing or responding to trade complaints.

Location: 20037, Washington, District Of Columbia
Phone: Not Available