The Pharma Data

MAY 13, 2021

Testimonials are not necessarily representative of all of those who will use our products. Some of our testimonials are provided by customers who have received promotional offers in exchange for their participation. The testimonials displayed are given verbatim except for correction of grammatical or typing errors. 2011-1034. .

Disease 52

Disease Production Testimonials Science 52

The Pharma Data

MAY 13, 2021

In a major double-blind clinical trial published in the American College of Endocrinology…. Which has been proven in numerous clinical trials to: Rhodiola is a flowering plant that grows in the remote regions of the Arctic… And in a major randomized, double-blind, and placebo-controlled study published in the Journal Planta Medica….

Production 52

Production Packaging Doctors Research 52

Drug & Device Law

DECEMBER 21, 2023

Never mind that, since Bausch the Supreme Court has entertained preemption issues under Rule 12(b)(6) on multiple occasions, including the Mensing ( 2011+1 ) prescription drug preemption decision. The only basis for that opinion was supposed “extensive research and experience” that the risk occurred “way more” than what the trials stated.

FDA Approval 52

FDA Approval FDA Drugs Production 52

Drug & Device Law

FEBRUARY 25, 2022

We return to a theme we’ve repeated twice before, in 2011 and in 2014 – that in addition to industry-specific groups, manufacturers of prescription medical products should definitely consider joining the Product Liability Advisory Council (“PLAC”). Notice how admissibility of expert testimony under Fed. 19-2899 (8th Cir. filed Sept.

Testimonials 59

Testimonials Production Drugs Pharmaceuticals 59

Drug & Device Law

DECEMBER 29, 2023

2023) (remote trial testimony cannot be compelled beyond Rule 45’s 100-mile limit on subpoenas) ( here ); Carson v. They excluded bogus expert testimony under Fed. Thus, CEH turned on implied impossibility preemption, specifically an application of Mensing ( 2011+1 ) independence principle. Bonta , 85 F.4th

Testimonials 105

Testimonials FDA Drugs Vaccine 105

Drug & Device Law

FEBRUARY 20, 2023

For several decades – starting with plaintiffs’ pre-Vaccine Act attacks on vaccine designs – courts have addressed FDA approval as a component of “feasibility” in states that impose this limitation on design defect claims. Or does it suffice that a vaccine design has been approved in other countries? In Bruesewitz v.

FDA 59

FDA FDA Approval Testimonials Vaccine 59