Clarivate

MAY 24, 2022

Recent policy and regulatory moves have begun to sketch out a framework for rare disease drug approvals in the country, but obstacles to approvals and patient access remain. The list, designed to serve as a reference point for prioritized drug review and evaluation policies, included 121 rare diseases. [8]. 10] [11] [12].

Patients 52

Patients Food and Drug Administration Marketing Pharma 52

European Pharmaceutical Review

SEPTEMBER 21, 2023

In this Q&A, Karen Pinachyan, Head of Medical Affairs Europe at CSL Behring summarises key considerations for gene therapy drug development and the ideal approach for alleviating economic strain when advancing these modern treatments. The US Food and Drug Administration (FDA) requires a patient follow up period of at least 10-15 years.

Pharmaceutical 74

Pharmaceutical Food and Drug Administration Medicine Manufacturing 74

Legacy MEDSearch

JUNE 10, 2022

a leading US developer of next gen endoscope systems announces today the US Food and Drug Administration (FDA) has granted 510(k) clearance of its novel integrated 360° field of view colonoscope. See Full Press Release at the Source: Saneso Novel 360° Colonoscope Receives FDA Clearance. Saneso Inc.,

FDA 52

FDA Food and Drug Administration Recruitment Physicians 52

pharmaphorum

OCTOBER 3, 2022

This typically sees higher-priced drugs, even in oncology, being sidelined in favour of biosimilars, off-patent branded drugs, or locally manufactured alternatives, unless manufacturers offer significant discounting to gain access to national essential medicines lists. The power rests with Europe and the UK.

Food and Drug Administration 91

Food and Drug Administration Consulting Marketing Manufacturing 91

Pharmaceutical Technology

JUNE 30, 2022

Another factor driving Georgia’s growth in the clinical trial space is the recent significant investment in the country’s health system, creating several new facilities and programmes, as well as increasing the number of experienced physicians.

Food and Drug Administration 52

Food and Drug Administration Distribution Recruitment Transportation 52

Pharma Marketing Network

JUNE 11, 2020

I was at Physicians Online at the time. Yeah, I even wanted to wear the shirt to this FDA meeting. You know, in November 2009, the FDA held a public hearing about the promotion of Food and Drug Administrative Related Regulated Medical Products, using the internet and social media tools.

Media 52

Media Pharma Ethics Consulting 52

Legacy MEDSearch

JULY 20, 2023

Food and Drug Administration (“FDA”) for its XR90 augmented reality-based surgical visualization and navigation platform. “MediView is excited to receive 510(k) clearance for our XR90 platform and appreciate the team’s efforts and FDA’s partnership in achieving this milestone. .”

FDA 52

FDA Food and Drug Administration Recruitment Healthcare 52

Cadensee

JULY 20, 2021

Basically, I started teaching myself how to get good information outside the internet and see how that empowers us with our discussion with a physician with everything that we did. It might be silly question but bringing a drug to market takes many, many years. So, I myself, was kind of tasked with go and search on the internet.

Food and Drug Administration 52

Food and Drug Administration Doctors Healthcare Healthcare 52