Leads, Safety, Side effects and Training

How to Boost Pharma Sales AI Training with AI Insights

Quantified

MAY 2, 2024

In response, forward-thinking corporate decision-makers nationwide are turning to cutting-edge pharma sales AI training to optimize the impact of every human interaction. AI-supported training platforms offering life-like detailing simulations, on the other hand, are designed to assess human interactions objectively.

Training

Training Sales Pharma Sales Management

Leading speciality pharmacies in pharma

Pharmaceutical Technology

SEPTEMBER 8, 2022

Speciality pharmacies play a crucial role in medication dosing, disease and side effects management, and patient care. Patient education and medication adverse effect counselling. Patient monitoring for safety and efficacy. The post Leading speciality pharmacies in pharma appeared first on Pharmaceutical Technology.

Specialization

Specialization Leads Pharma Side effects

How Artificial Intelligence Could Be the Ultimate Weapon Against Cancer

MedCity News

JANUARY 30, 2024

With the rise of AI technologies, we could see significant advancements in cancer treatment, making it more efficient and potentially leading to a cure. By analyzing vast amounts of data from medical records, laboratory tests and imaging scans, AI algorithms can provide a more precise diagnosis, which can lead to better treatment outcomes.

Side effects

Side effects Ethics Medical Patients

Tributes as former NICE, MHRA chair Sir Mike Rawlins dies

pharmaphorum

JANUARY 3, 2023

A pharmacologist by training, Rawlins was the founding chairman of health technology assessment (HTA) agency NICE , leading the organisation from its inception in 1999 until 2013, and hired Sir Andrew Dillon to become the organisation’s founding chief executive.

Side effects

Side effects Medicine Safety Healthcare

Understanding the evidence used in drug product withdrawals

European Pharmaceutical Review

DECEMBER 14, 2023

Over the past few years, we have researched the types of evidence used in regulatory decisions for drug product withdrawals due to safety concerns in Europe. But from a safety point of view, observational studies can be more representative of the population the drug will serve. Lane S, Lynn E, Shakir S.

Safety

Safety Medicine Competition Networking

Developing a first-in-class small molecule drug for inflammatory disease

European Pharmaceutical Review

NOVEMBER 9, 2023

Positively, Brager shared that in clinical trials , the company’s lead clinical candidate has demonstrated ability to cross the blood-brain barrier and to “not cause serious side effects common with traditional immunosuppressive therapies that treat inflammation.” This allows us to stay on top of quality control.

Food and Drug Administration

Food and Drug Administration Side effects Pharmaceutical Leads

Streamlining healthcare with AI for drug development

Pharmaceutical Technology

JUNE 15, 2023

Developing safe and effective drugs Pharma researchers are using AI in the earliest stages. They’re also deploying AI to predict how new drugs will interact with the human body — and what side effects might arise. AI’s ability to analyze data quickly also contributes to safety, including during clinical trials.

Healthcare

Healthcare Healthcare Safety Ethics

New Study Demonstrates Consistent Positive Long-Term Adherence and Efficacy of Nerivio® for Treatment of Migraine

Legacy MEDSearch

OCTOBER 25, 2023

Theranica , a neuromodulation therapeutics company, announced the publication of a comprehensive clinical study in Advances in Therapy examining the long-term utilization, clinical efficacy, and safety of Nerivio ® , a Remote Electrical Neuromodulation (REN) device for the treatment of migraine. As for clinical efficacy, 74.1%

Side effects

Side effects Recruitment Networking Management

Drug repurposing, real world data and AI/ML: perspectives and opportunities

Clarivate

OCTOBER 19, 2023

Drug candidates have a high rate of failure, as only 10% of de-novo drugs put through clinical trials finally obtain market approval, with the highest rate of attrition occurring at phase I and II of clinical trials (assessing safety, tolerability, dosage, efficacy, and side effects).

Networking

Networking Consulting Safety Side effects

What DTC marketers can learn from people who refuse vaccines

World of DTC Marketing

SEPTEMBER 27, 2021

The reasons for people refusing vaccines are both safety and side effect concerns, although politics plays a big part as well. The drug, which FDA advisors refused to approve, has more side effects than initially anticipated, and of course, the media is running with the story, which, in turn, leads to a lack of trust in the FDA.

Side effects

Side effects Marketing Media FDA

Psilocybin-assisted therapy reduces depressive symptoms in cancer patients

European Pharmaceutical Review

DECEMBER 18, 2023

Treatment-related side effects included nausea and headache but were generally mild. “As As an oncologist for many years, I experienced the frustration of not being able to provide cancer care that treats the whole person, not just the tumour,” commented Manish Agrawal, MD, of Sunstone Therapies and lead author of the study.

Food and Drug Administration

Food and Drug Administration Patients Side effects Safety

How to Work with Patient Advocates, Influencers, and Ambassadors

PM360

JUNE 11, 2022

Be clear in your governance documents and training to level set expectations. Then, the MRL team and the influencer must align on where there is flexibility within messaging while still abiding to brand safety guidelines, as you don’t want to lose the authenticity that the influencer brings. A Patient-Centric Month Leads to Results.

Patients

Patients Pharma Education Media

Developing point-of-care CAR T manufacturing

European Pharmaceutical Review

DECEMBER 27, 2023

4 Manufacturing of CAR T-cell therapies: an overview In addition, multi-disciplinary teams must be established for in-house CAR T-cell therapy programmes to ensure maximum success and safety. On the logistics side, the in-house process eliminates, in principle, the need for cryopreservation of the CAR T-cell products.

Manufacturing

Manufacturing Food and Drug Administration Patients Pharma

Telehealth in the 2022 Medicare Physician Fee Schedule: Audio-Only Telehealth for Mental Health Made Permanent, and CMS Punts on Remote Direct Supervision

Nixon Gwilt Law

NOVEMBER 5, 2021

Citing MedPAC’s concerns about patient safety, CMS declined to address this in the final rule, stating that the agency will consider addressing the issues raised by these comments in future rules or guidance, as appropriate.

Physicians

Physicians Professional Services Side effects Medical

Pharma Rep Focus

How to Boost Pharma Sales AI Training with AI Insights

Leading speciality pharmacies in pharma

Trending Sources

How Artificial Intelligence Could Be the Ultimate Weapon Against Cancer

Tributes as former NICE, MHRA chair Sir Mike Rawlins dies

Understanding the evidence used in drug product withdrawals

Developing a first-in-class small molecule drug for inflammatory disease

Streamlining healthcare with AI for drug development

New Study Demonstrates Consistent Positive Long-Term Adherence and Efficacy of Nerivio® for Treatment of Migraine

Drug repurposing, real world data and AI/ML: perspectives and opportunities

What DTC marketers can learn from people who refuse vaccines

Psilocybin-assisted therapy reduces depressive symptoms in cancer patients

How to Work with Patient Advocates, Influencers, and Ambassadors

Developing point-of-care CAR T manufacturing

Telehealth in the 2022 Medicare Physician Fee Schedule: Audio-Only Telehealth for Mental Health Made Permanent, and CMS Punts on Remote Direct Supervision

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