pharmaphorum

AUGUST 17, 2020

In this article Joanna Carlish, managing director of financial services at Tag Americas , and Robb DeFilippis, Tag Americas’ managing director, life sciences, go head-to-head to discuss marketing within a regulated industry. How are regulated industries approaching the personalisation, or even hyper-personalisation, of content?

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Regulation Marketing Sales Branding 91

Rethinking Clinical Trials

SEPTEMBER 13, 2023

For the RSI trial the FDA regulations had not been updated yet. Tags #pctGR, @Collaboratory1 The post Grand Rounds September 8, 2023: The DEVICE Trial: An Embedded, Pragmatic Trial of Emergency Airway Management (Matthew Prekker, MD, MPH; Jonathan Casey, MD, MSc) appeared first on Rethinking Clinical Trials.

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Trials Clinical Trials Clinical Trials Medicine 141

Rethinking Clinical Trials

FEBRUARY 16, 2023

The regulations recognize that consent is not always possible and allow for alteration, where some of the required elements of informed consent can be altered or not included, and waiver of consent, where no consent is required. Opt-outs were different across health systems. Pearl O’Rourke, MD; David S.

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Clinical Trials Clinical Trials Medicine Trials 130

Rethinking Clinical Trials

JULY 6, 2023

There has been a growing sense of hesitancy about whether regulators will remain equally receptive to these decentralized methods when the pandemic recedes. During the COVID-19 pandemic, several regulatory authorities around the world introduced guidance on DCTs.

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Trials Clinical Trials Clinical Trials Licensing 130

pharmaphorum

AUGUST 21, 2022

Shares in Axsome Therapeutics have rocketed on FDA approval of its depression therapy Auvelity (formerly AXS-05) – a year after its approval was held up by the regulator. Auvelity is the first drug Axsome has taken through to regulatory approval, but could be the first of a string of new products for the company, according to Tabuteau.

Drugs 98

Drugs FDA Approval Production Marketing 98

Rethinking Clinical Trials

JANUARY 19, 2023

Tags #pctGR, @Collaboratory1 The post Grand Rounds Ethics and Regulatory Series January 13, 2023: Ethical Considerations When Vulnerable Populations are Subjects in Pragmatic Trials (Emily A. – What if a patient has capacity to consent but their surrogate disagrees? That’s difficult. it can be a barrier.

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Trials Clinical Trials Clinical Trials Research 130

FDA Law Blog

JULY 20, 2021

The new rule applies not only to product labeling, but to any “mail order catalog” or “mail order promotional material” that includes a seal, mark, tag, or stamp that labels a product as having been made in the United States. However, this list is not exhaustive. or the Egg Products Inspection Act.

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Production Sales Regulation Packaging 76

Rethinking Clinical Trials

OCTOBER 27, 2022

Should social media for teenagers be regulated like a digital therapeutic, given how addictive they are and the behavior modification. Case study: The U.K. The Light Collective is an organization that represents collective rights, interests, and voices of patient communities in healthcare technology. pctGR, @Collaboratory1.

Clinical Research 130

Clinical Research Research Clinical Trials Clinical Trials 130

pharmaphorum

APRIL 20, 2021

Novartis has secured backing from NICE for its relapsing multiple sclerosis (RMS) therapy Kesimpta in the UK, just two weeks after the drug was approved by the national drugs regulator. . The Scottish Medicines Consortium is expected to publish its final advice on the drug later this year.

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Sales Medicine Drugs Marketing 110

Pharmaceutical Technology

APRIL 5, 2023

But access to these treatments continues to remain limited due to high price tags and variable availability across regions. AZ: How can regulators ensure that they nurture future innovations in the field? Across the world, to varying degrees, the regulations were written in an era of small molecules and biologics.

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Gene Therapy Gene Engineer Production 147

XTalks

JUNE 28, 2023

million price tag of Elevidys, a one-time gene therapy. The FDA approval came after several delays and a narrow advisory committee vote of eight to six in favor of the gene therapy’s risk-benefit profile. In a media call, Sarepta CEO Douglas Ingram revealed the $3.2

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Gene Therapy Gene Protein FDA Approval 98

XTalks

JANUARY 28, 2022

Immunocore received Breakthrough Device Designation for Kimmtrak from the FDA in February 2021 followed by acceptance of its Biologics License Application (BLA) several months later by both US and European regulators. Kimmtrak has a price tag of $18,760 per vial, which amounts to a weekly dose.

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FDA Approval Development Licensing Licensing 98

pharmaphorum

SEPTEMBER 15, 2020

Pharma’s go-to-market strategies have tended to be more traditional than those seen in non-regulated sectors, but there are some signs this is changing, with an acceleration in the pace of change forced by the COVID-19 pandemic that is allowing the industry to close its gap with faster, more nimble consumer brands. Jeremy Richter, Tag.

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Branding Marketing Pharma Companies Life Science 118

The Pharma Data

MARCH 7, 2022

The new technique controls gene activity without altering the DNA sequence of the genome by targeting chemical modifications that help package genes in our chromosomes and regulate their activity. The chemical modifications that regulate gene activity are called epigenetic markers. Cas9 binds and uses RNA as an address-tag.

Protein 52

Protein Gene Genome Genomics 52

Rethinking Clinical Trials

AUGUST 28, 2023

The International Council for Harmonisation of Technical Requirements for Human Use (ICH) is a unique harmonization organization involving regulators and the pharmaceutical industry. One important note is that we specifically moved away from a checklist approach. The guidance should not remove the need to think.

Clinical Trials 130

Clinical Trials Clinical Trials Trials Development 130

Rethinking Clinical Trials

AUGUST 28, 2023

The International Council for Harmonisation of Technical Requirements for Human Use (ICH) is a unique harmonization organization involving regulators and the pharmaceutical industry. One important note is that we specifically moved away from a checklist approach. The guidance should not remove the need to think.

Clinical Trials 130

Clinical Trials Clinical Trials Trials Development 130

The Pharma Data

MARCH 23, 2022

The researchers found that Ebola virus polymerase leverages host protein GSPT1 to positively regulate viral transcription – a process the virus uses to convert its genetic material into instructions for making viral proteins. . “To our surprise, Ebola virus can subvert host restriction imposed by GSPT1 and UPF1,” says Fang.

Protein 52

Protein Genome Genomics Research 52

pharmaphorum

MAY 17, 2021

There had been speculation that the FDA might approve Empaveli (pegcetacoplan) only as a backup option for patients who don’t see a sufficient benefit with Alexion’s Soliris (eculizumab) or Ultomiris (ravulizumab), but the regulator opted for a broad indication that included first-line treatment for PNH. billion and $1.1

Drugs 52

Drugs FDA Approval Marketing Clinical Trials 52

XTalks

APRIL 29, 2022

Tirzepatide is a novel investigational obesity treatment that contains mimetics of two hormones that are involved in regulating appetite in a single peptide: a GIP (glucose-dependent insulinotropic polypeptide) receptor agonist and a GLP-1 (glucagon-like peptide-1) receptor agonist. percent and 22.5 percent, respectively, compared to placebo.

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Trials Drugs FDA Approval Clinical Trials 98

Intouch Solutions

APRIL 11, 2024

In this highly regulated Industry, it has become necessary to address and manage issues related to Data Quality: quality and integrity are crucial for compliance. This iterative process yields several benefits, including: Creating clusters of customers based on actual physician behavior.

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Compliance Marketing Drugs Pharma Companies 52

Drug Discovery World

JANUARY 30, 2024

Other Challenges: Limited insurance coverage: Many insurance companies are hesitant to cover CGTs due to their high price tags and limited long-term data. Fostering open innovation and collaboration could help address this issue. Increased clinical data and evidence of cost-effectiveness can improve coverage.

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Gene Therapy Manufacturing Gene Clinical Trials 71

The Pharma Data

MAY 5, 2021

AbbVie’s Humira regains top pharma TV spender spot, while sibling brands Rinvoq and Skyrizi tag along ( Fierce ). My Conversation with Daniel Carpenter, on regulation and also the FDA ( Marginal Revolution ). The new EU AI regulation proposal, medical devices and IVDs ( Medicaldeviceslegal ).

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Vaccination Vaccine Gene Therapy Contract Packaging 52

XTalks

FEBRUARY 27, 2024

Despite high price tags of a couple of million dollars, gene therapy makers say they are working to ensure patients are able to access the treatments through patient assistance programs developed in conjunction with the support of governments. Sarepta hopes to clarify Elvidys’ effectiveness in older children in a confirmatory trial.

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Research Drugs Gene Therapy Clinical Trials 59

pharmaphorum

JUNE 2, 2022

This is why the action by the US in 1983 and subsequently the European Commission Regulation No. 141/2000 (the Orphan Regulation), that both acted to encourage development in the area, are regarded as crucial for changing the landscape in rare disease R&D. It is estimated that between 3.5 The price is right. Raising questions.

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Drugs Sales Marketing Development 52

The Pharma Data

OCTOBER 29, 2021

Merck has tagged to withdraw its Premerger Notification and Report Form, which was originally filed on October 14, 2021, to give the Federal Trade Commission (the “ FTC”) with fresh time for review, and expects to refile similar form on or about November 1, 2021. As a result, Astros Merger Sub,Inc. Eastern time, on November 18, 2021.

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Containment Regulation Vaccination Vaccine 52

Pharmacy Checkers

FEBRUARY 21, 2020

And in my comments to the FDA on Section 801 for Prescription Justice, I ask a lot of questions about how this might help create more regulated pathways for safe personal drug importation. Those contracts are based on NDC numbers, unique codes tagged to the drug package. And if that helps someone afford their medication, cool.

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Drugs FDA Approval Manufacturing Pharmacy 61

XTalks

MARCH 22, 2023

In addition, 2016 saw a six-fold increase in the number of complete response letters sent to drugmakers compared to 2015, requiring companies to take additional measures before the regulator would consider approval. In addition, nearly half of all new drugs launched between 2020 and 2021 came with a price tag of $150,000 per year, or more.

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Life Science Drugs FDA Approval Vaccination 97

Intouch Solutions

AUGUST 25, 2021

As noted, this is a user concern that is here to stay, and regulation has just begun. CX Strategist; Carol Wilbeck, Campaign Management Team Lead; Jackie Sallaz, Tagging Solutions Engineer; Angela Ornce, Senior Director, Media Operations. Stay educated on privacy updates! ©Intouch Group 2021. Want to learn more?

Marketing 52

Marketing Regulation Engineer Branding 52

Cloudbyz

JUNE 1, 2023

Comprehensive Compliance Salesforce offers a comprehensive suite of compliance features to ensure data privacy, security, and adherence to various industry regulations. This can be critical for compliance with many regulations. government data).

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Compliance Development Branding Production 82

pharmaphorum

AUGUST 26, 2022

BioMarin will no doubt have an eye on the earlier experience of bluebird bio, which secured EU approval for rare disease gene therapy Zynteglo (betibeglogene autotemcel) in 2019 for beta thalassaemia with a price tag of around €1.6 million spread over five years.

Gene Therapy 110

Gene Therapy Gene Antibody Marketing 110

Drug Discovery World

NOVEMBER 13, 2023

Michael Traxlmayr, PhD, Group leader, CD Laboratory for Next-Generation CAR T Cells, University of Natural Resources & Life Sciences, on: ‘Novel concepts to regulate CAR T cell activity with small molecule drugs in vivo’.

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Protein Antibody Engineer Scientist 59

pharmaphorum

SEPTEMBER 30, 2022

The traceability of components is critical for authoring structured content correctly, especially when it comes to fulfilling compliance regulations. While a single document might only be re-used a couple of times, if at all, components of that document might be re-used a hundred times across multiple applications.

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Compliance Life Science Marketing Production 52

The Pharma Data

MAY 4, 2021

healthcare reform or legislation or any significant spending reductions or cost controls affecting Medicare, Medicaid or other publicly funded or subsidized health programs or changes in the tax treatment of employer-sponsored health insurance that may be implemented; U.S. View source version on businesswire.com : [link]. Amy Rose 212.733.7410.

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Vaccination Vaccine Production Sales 40

World of DTC Marketing

JUNE 16, 2021

The May 2021 KFF Health Tracking Poll finds about two-thirds of adults say there is “not as much regulation as there should be” when it comes to limiting the price of prescription drugs. About eight in ten across partisans say profits made by pharmaceutical companies are a “major factor” in the price of prescription drugs.

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Drugs Branding Medicine Insulin 180