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news April 21, 2020

Amin Talati Continues to Expand Its Medical Device Practice With Addition of Partner

Leading regulatory and intellectual property law firm Amin Talati Wasserman LLP today announced that prominent medical device attorney Evan Phelps has joined the firm as a partner in Washington, D.C. CHICAGO (PRWEB) APRIL 21, 2020 Evan Phelps advises medical device companies around the globe on a wide variety of FDA legal and regulatory matters, including Premarket […]

publication April 15, 2020

DSHEA Provisions Confine FDA’s Authority to Issue Regulations That Concern Allegedly Adulterated Dietary Supplements, (Co-Author), 54 Food and Drug Law Journal 595-598, 1999.

DSHEA Provisions Confine FDA's Authority to Issue Regulations That Concern Allegedly Adulterated Dietary Supplements, (Co-Author), 54 Food and Drug Law Journal 595-598, 1999.

publication April 15, 2020

The Role of the Clinician and Health Care Facility in Medical Device Safety – Adverse Medical Device Reporting, Teaching Hospitals & Academic Medical Centers, June, 2007.

The Role of the Clinician and Health Care Facility in Medical Device Safety - Adverse Medical Device Reporting, Teaching Hospitals & Academic Medical Centers, June, 2007.

publication April 15, 2020

The Role of PTs in Medical Device Safety: Adverse Medical Device, Physical Therapy Reimbursement News, Vol. 15, No. 1, January/February, 2008.

publication April 15, 2020

Reporting Adverse Events: Physical Therapists and Treatment Centers Play a Role in Medical Device Safety, Advance, Vol. 20, Issue 5, 2009.

publication April 15, 2020

Medical Device Regulation & Compliance, Food Drug and Law Institute, 2010.

news March 10, 2020

Expert in FDA Law Formulated ABCs of CBD at Mingle

Author: Bob Benenson, Naturally Chicago March 10th, 2020 Since launching his first law firm in 1998, Rakesh Amin has built a practice representing hundreds of companies that produce food and beverages, dietary supplements and cosmetics. His work in this sector has earned him regard as the nation’s leading expert in law pertaining to the regulatory authority […]

news February 26, 2020

Will 2020 Provide A Clearer Vision for CBD? A Lookback at 2019 and Predictions for the New Year.

By: Suzanne Bassett A year has passed since the 2018 Farm Bill was signed into law legalizing hemp and hemp-derived products, including cannabinoids, with no more than 0.3% tetahydrocannabinol (THC).[1] However, the regulatory status of cannabidiol (CBD) finished products regulated by the Food and Drug Administration has not been easy sailing with several federal and […]

Amin Talati Continues to Expand Its Medical Device Practice With Addition of Partner

DSHEA Provisions Confine FDA’s Authority to Issue Regulations That Concern Allegedly Adulterated Dietary Supplements, (Co-Author), 54 Food and Drug Law Journal 595-598, 1999.

The Role of the Clinician and Health Care Facility in Medical Device Safety – Adverse Medical Device Reporting, Teaching Hospitals & Academic Medical Centers, June, 2007.

The Role of PTs in Medical Device Safety: Adverse Medical Device, Physical Therapy Reimbursement News, Vol. 15, No. 1, January/February, 2008.

Reporting Adverse Events: Physical Therapists and Treatment Centers Play a Role in Medical Device Safety, Advance, Vol. 20, Issue 5, 2009.

Medical Device Regulation & Compliance, Food Drug and Law Institute, 2010.

Expert in FDA Law Formulated ABCs of CBD at Mingle

Will 2020 Provide A Clearer Vision for CBD? A Lookback at 2019 and Predictions for the New Year.

Accomplished Litigator George Spatz Joins Amin Talati; Will Lead Ligation Practice

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