Pharmaceutical Technology

SEPTEMBER 1, 2022

In molecular devices, you have a lot of processes, and they are very complex because you are dealing with different reagents and with a variety of materials. “For strip devices, you have just a few processes for the device assembly,” says Jean-François Bauer, head of marketing and business development at Mikron Automation. “In

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Roots Analysis

AUGUST 29, 2023

Raw materials used for the production of cell therapies include culture media, growth factors, extracellular matrices and reagents. Types of Cell Therapy Consumables Raw materials used in the manufacturing of cell therapies can be classified as buffers, cell culture media, growth factors, kits, reagents and extracellular matrices.

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XTalks

JANUARY 21, 2025

In a clinical trial, participants demonstrated a 98% success rate after six months post implantation, with arteries widened successfully and no stent fractures observed. In a trial with 100 patients , the device demonstrated no major complications, an average bleeding stop time of 2 minutes, with patients walking within approximately 2.5

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The Pharma Data

OCTOBER 14, 2020

A paper on the clinical trial results published in JAMA Oncology demonstrates the effectiveness of Savran Tech’s CTC detection technology with real world patients. The trial involved about 200 patients with early stage triple negative breast cancer who received chemotherapy and underwent surgery. About This Clinical Trial.

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pharmaphorum

FEBRUARY 3, 2021

While achieving the Nobel Prize spotlight would have been enough to impress, CRISPR-Cas9 gene editing is part of a growing list of technologies granted Investigational New Drug (IND) applications with early data from clinical trials supporting its safe use in edited cells re-introduced into a patient.

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pharmaphorum

SEPTEMBER 29, 2022

She regularly drafts and negotiates agreements required for the development and commercialization of pharmaceutical and medical device products, including licensing agreements, collaboration agreements, clinical trial agreements, and an array of services agreements.

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The Pharma Data

AUGUST 19, 2021

Continued approval for this indication may depend on verification and description of clinical benefit in a confirmatory trial(s). This indication received accelerated approval based on tumour response rate and durability of response. Read more about Roche innovation in MMR biomarker testing.

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FDA Approval DNA Reagent Protein 52

pharmaphorum

JANUARY 25, 2022

The Toronto-based company already counts many of the world’s largest pharma companies among its customers, using its platform for a range of tasks such as improving reagent and antibody selection to help scientists run more successful experiments, drawing on data from published studies and organisations’ internal databases.

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The Pharma Data

MAY 17, 2021

Now these entities are being increasingly sought out to develop these therapies as more applications are being explored, especially with the “groundbreaking results” of these trials in the oncology areas. . With this explosive growth, “the need for clinical testing and application facilities is growing steadily,” said Uharek. .

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pharmaphorum

DECEMBER 16, 2022

Clinical trials technology company Saama has hired Dr Clinton White as its new chief delivery officer. Reagents supplier The Native Antigen Company has hired a new business development manager, Richard White , and senior product manager, Pardeep Sharda.

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Behavioural Health Reagent Gene Therapy Production 52

The Pharma Data

OCTOBER 19, 2020

DB ( Becton, Dickinson and Company ) received a CE mark for its BD Multitest 6-Color TBNK Reagent with BD Trucount Tubes for assessing immune function in COVID-19 patients. There has been some discussion of running challenge trials for COVID-19 vaccines. The trials won’t begin until early 2021 and are expected to finish in May 2021.

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The Pharma Data

DECEMBER 23, 2020

The agreement includes a £500,000 upfront payment to Avacta which gives Astrea the rights to generate and develop Affimer reagents in-house for affinity separation. The FOCUS trial is Ultimovacs’ fourth Phase II clinical trial with UV1 and comes in addition to the collaboration Phase II trial announced in May 2020.

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Advarra

NOVEMBER 29, 2022

Bottlenecks in the manufacturing process, supply chain issues such as accessibility of good manufacturing practice (GMP)-grade reagents, and shortages of qualified scientists and engineers have caused many therapies to fail at critical stages of the clinical development pipeline. But review issues are not the only problems.

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Gene Therapy Gene Production Clinical Trials 52

The Pharma Data

OCTOBER 14, 2020

The designation of lanifibranor as a Breakthrough Therapy for the treatment of NASH follows the publication in June 2020 of positive topline results from Inventiva’s NATIVE Phase IIb clinical trial with lanifibranor in NASH patients. The trial plans to evaluate safety, tolerability, cytokine profile and efficacy parameters.

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Clinical Trials Clinical Trials Manufacturing In-Vivo 52

pharmaphorum

JUNE 1, 2021

This technology can also play an important role in supporting virtual clinical trials. The FDA has stated that when microtaggants are pharmaceutically inactive and incorporated into new or existing drugs, they can be treated as excipients without the need for further clinical trials. The threat of illegal online pharmacies.

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The Pharma Data

MAY 15, 2023

She is also a board member at BBI Solutions, a UK based diagnostic reagents and a Novo Holdings company. Since 2012, she serves as board member and currently as chair of the Audit Committee of Tecan Group, a Swiss listed company.

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XTalks

OCTOBER 1, 2020

The drug is currently in clinical trials for alcoholic hepatitis (AH), nonalcoholic steatohepatitis (NASH), as well as in COVID-19 patients with acute liver or kidney injury. Key Moments. Now she says that she completely appreciates the focus of industry. But in companies, you cannot do that.

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XTalks

JANUARY 6, 2025

For example, antisense oligonucleotide (ASO)-based therapies have gained traction, with 100 Phase I clinical trials initiated and around 25 percent of these advancing to Phase II or Phase III trials in recent years. The global next-generation biomanufacturing market is projected to grow at a CAGR of 14.85 billion by 2031.

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