Clinical Supply, Clinical Trials and Regulation

Importer of Record for Clinical Trials

Imperical Blog

SEPTEMBER 7, 2023

Avoiding “Customs Chaos” in Clinical Trials Means Working Closely with Your Importer of Record Many global clinical trial shipments get muddled regarding the critical role and responsibilities of the importer of record (IOR) for clinical trials.

Clinical Trials

Clinical Trials Clinical Trials Trials Clinical Research

Importer of Record for Clinical Trials

Imperical Blog

SEPTEMBER 7, 2023

Avoiding “Customs Chaos” in Clinical Trials Means Working Closely with Your Importer of Record Many global clinical trial shipments get muddled regarding the critical role and responsibilities of the importer of record (IOR) for clinical trials.

Clinical Trials

Clinical Trials Clinical Trials Trials Clinical Research

Clinical Trial Data: Navigating Audit Trail Data Regulations and Accessibility Challenges

VirTrial

APRIL 18, 2024

Data is the single most important thing in a clinical trial. The data serves as the cornerstone for critical decisions determining the fate of therapies and the performance of trials. The data highlights fast or slow recruitment and how the drug supply is managed.

Regulation

Regulation Clinical Trials Clinical Trials Trials

Untangling the Complexities of Cell and Gene Therapy Clinical Trials: A Supply Chain Perspective

Pharmaceutical Technology

MAY 24, 2023

By Luisa Sterkel & Joana Loureiro , Tenthpin Consultants The promise and potential of cell and gene therapies (CGT) has emerged in the recent past and currently over 1.500 CGT are registered for clinical trials holding great hope for the treatment of challenging and uncurable diseases.

Clinical Trials

Clinical Trials Clinical Trials Gene Therapy Clinical Supply Chain

Why and How Will Ecommerce Transform the Interactive Response Technology (IRT) User Experience?

XTalks

APRIL 6, 2023

Modern software development concepts from ecommerce applications are helping eClinical applications meet the precise needs of each clinical trial. IRT solutions help clinical trial sponsors meet the complexities of patient randomization and clinical supply management. until the database lock of the system.

Clinical Trials

Clinical Trials Clinical Trials Clinical Supply Trials

MorphoSys To Present At the 39th Annual J.P. Morgan Healthcare Conference

The Pharma Data

JANUARY 10, 2021

For more information, please contact: SOURCE: MorphoSys AG via EQS Newswire. View source version on accesswire.com: [link]. Source link.

Containment

Containment Clinical Development Antibody Development

The Chemotherapy Drug Shortage: An Unprecedented Crisis

XTalks

JUNE 16, 2023

XTALKS WEBINAR: Fostering Patient-Centricity: Clinical Supply Chain Strategies and Sourcing Solutions Live and On-Demand: Thursday, July 20, 2023, at 10am EDT (4pm CEST/EU-Central) Register for this free webinar to learn how to review clinical trial trends and supply strategies that impact the patient experience.

Drugs

Drugs Manufacturing Clinical Supply Chain Clinical Trials

PharmaDrug Enters Definitive Agreement for Acquisition of Sairiyo Therapeutics Inc. Who Recently Received Orphan Drug Designation from FDA for Esophageal Cancer

The Pharma Data

JANUARY 24, 2021

In clinical research, Cepharanthine exhibits multiple pharmacological properties including anti-oxidative, anti-inflammatory, immuno-regulatory, anti-cancer, anti-viral and anti-parasitic properties. Sairiyo is currently focused on advancing the clinical development of Cepharanthine to treat rare cancer diseases.

Drugs

Drugs Containment Development Sales

Overcoming inefficiencies to improve access to cell and gene therapy

Drug Discovery World

MARCH 13, 2023

Between the 24 therapies already approved by the FDA 1 and a marked increase in clinical trials, widespread accessibility to precision medicine feels within reach. Drug discovery researchers usually partner with a CDMO to provide support through the development, manufacturing, and clinical supply required to bring a drug to market.

Gene Therapy

Gene Therapy Gene Manufacturing Development

VTX-801 RECEIVES U.S. FDA FAST TRACK DESIGNATION FOR THE TREATMENT OF WILSON DISEASE

The Pharma Data

AUGUST 15, 2021

Food and Drug Administration (FDA) has granted Fast Track designation to VTX-801, Vivet’s clinical-stage gene therapy for the treatment of Wilson Disease – a rare, genetic disorder that reduces the ability of the liver and other tissues to regulate copper levels, causing severe hepatic damage, neurological symptoms, and potentially death.

Gene Therapy

Gene Therapy Gene Clinical Trials Clinical Trials

A supply chain to match the changing face of science

Drug Discovery World

NOVEMBER 3, 2022

1 Emily was a seven-year-old girl who relapsed a second time following two years battling leukaemia, out of standard treatment options, and her life was saved by a CAR-T treatment in early clinical trial. The post A supply chain to match the changing face of science appeared first on Drug Discovery World (DDW). References .

Gene Therapy

Gene Therapy Production Development Business Development

Africa: Unleashing the potential of the new superpower in clinical trials

Pharmaceutical Technology

MARCH 20, 2023

Africa has considerable advantages and opportunities for trialling investigational medicinal products that, if pharma companies can correctly harness, will turn the continent into a superpower for clinical trials. Clinical trials data for Africa Globally, research has found that 62.2% being African American, 3.4%

Clinical Trials

Clinical Trials Clinical Trials Trials Clinical Supply Chain

Clinical Research Informer

Importer of Record for Clinical Trials

Importer of Record for Clinical Trials

Trending Sources

Clinical Trial Data: Navigating Audit Trail Data Regulations and Accessibility Challenges

Untangling the Complexities of Cell and Gene Therapy Clinical Trials: A Supply Chain Perspective

Why and How Will Ecommerce Transform the Interactive Response Technology (IRT) User Experience?

MorphoSys To Present At the 39th Annual J.P. Morgan Healthcare Conference

The Chemotherapy Drug Shortage: An Unprecedented Crisis

PharmaDrug Enters Definitive Agreement for Acquisition of Sairiyo Therapeutics Inc. Who Recently Received Orphan Drug Designation from FDA for Esophageal Cancer

Overcoming inefficiencies to improve access to cell and gene therapy

VTX-801 RECEIVES U.S. FDA FAST TRACK DESIGNATION FOR THE TREATMENT OF WILSON DISEASE

A supply chain to match the changing face of science

Africa: Unleashing the potential of the new superpower in clinical trials

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