European Pharmaceutical Review

APRIL 8, 2024

Biopharmaceuticals contributing to manufacturing outsourcing trend Increased outsourcing activity A survey conducted by the authors indicated that the role of CDMOs in the mAbs industry has changed since 2010, approximately.

Manufacturing 52

Manufacturing Networking Pharmaceutical Marketing 52

Pharma Pathway

JANUARY 12, 2023

Ltd was incorporated in January 2010 and was founded by a group of experienced industry professionals. SunGlow Lifescience Pvt. Ltd-Openings for Production/ QC/ RA/ QMS/ ARD/ FRD/ Boiler Operator Dept. Job Description. SunGlow Lifescience Pvt. Our Corporate office is located in Chennai, Indian.

Manufacturing 79

Manufacturing Marketing 79

European Pharmaceutical Review

APRIL 2, 2024

Before joining Siegfried in 2010, Wienand worked at the German specialty chemicals company Evonik Industries, Lonza highlighted. Baehny has held his Chief Executive Officer ad interim role since October 2023 and will support Wienand through the transition period.

Biopharma 98

Biopharma Leads Manufacturing Pharmaceutical 98

PharmaTech

AUGUST 29, 2022

Moderna is suing Pfizer and BioNTech for allegedly infringing on patents the company filed from 2010 to 2016.

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European Pharmaceutical Review

AUGUST 26, 2022

Moderna has filed patent infringement lawsuits alleging that Pfizer and BioNTech’s COVID-19 vaccine Comirnaty ® infringes patents Moderna filed between 2010 and 2016 covering its foundational messenger RNA (mRNA) technology.

Sales 98

Sales Medicine Marketing Government 98

European Pharmaceutical Review

DECEMBER 13, 2022

USP-NF Propylene Glycol Monograph: USP43-NF38, 2010, 3753. 5 Both compounds are limited to ≤0.1 percent or 1,000 ppm. Elixirs, diluents, and the passage of the 1938 Federal Food, Drug and Cosmetic Act. Ann Intern Med. 122(6); 1995: 456-461. FDA Guidance for Industry Testing of Glycerin for Diethylene Glycol. SCCP OPINION ON Diethylene glycol.

Food and Drug Administration 105

Food and Drug Administration Manufacturing Safety Food 105

European Pharmaceutical Review

SEPTEMBER 18, 2023

Since 2010, the sector has secured eight percent growth each year. CGT Catapult aims to foster more connections, collaborations and partnerships between academia and industry to advance the sector, the organisation declared.

Networking 117

Networking Medicine Manufacturing Medical 117

Pharma Pathway

JANUARY 31, 2023

Ltd was incorporated in January 2010 and was founded by a group of experienced industry professionals. Ltd-Walk-In Interviews for Production/ QC/ RA/ QMS/ ARD/ FRD/ Boiler Operator/ Maintenance/ Engineering/ Warehouse/ Regulatory Affairs/ QA On 5th Feb’ 2023 Job Description SunGlow Lifescience Pvt.

Engineering 86

Engineering Manufacturing Marketing Management 86

Medico Reach

AUGUST 18, 2022

Founder: Graham Gardner Year of Establishment: 2010 Headquarters: Boston, Massachusetts. Founder: Grant Verstandig Year of establishment: 2010 Headquarters: Washington, DC. Founder: Jeff Tangney Year of establishment: 2010 Headquarters: San Francisco, California. In doing so, it helps to make each cancer patient’s story count.

Healthcare 98

Healthcare Healthcare Medical Doctors 98

World of DTC Marketing

MAY 2, 2021

According to data from KFF’s annual survey of employers , between 2010 and 2020, insurance premiums for employer-sponsored family coverage rose by 55 percent; the employer’s contribution went up 61 percent. The average family policy now costs over $21,000, most of which is paid by the employer.

Healthcare 277

Healthcare Healthcare Insurance Government 277

World of DTC Marketing

JUNE 6, 2022

According to an AARP study, in 2010 there were 7 potential caregivers for every person over 80. The rest were additional approvals of an existing drug or first approvals of a “me-too” drug that enters an existing class of treatment. Care Giving Crisis.

Healthcare 174

Healthcare Healthcare Food Government 174

European Pharmaceutical Review

MARCH 31, 2023

billion in total venture financing raised from 2010 to 2022 for drug development In 2018 alone, the company invested over $400 million in venture financing. GlobalData Pharma Intelligence Center Deals Database found: SVB Financial Group and its subsidiaries were involved in more than $1.4

Biopharma 98

Biopharma Pharma Networking Marketing 98

European Pharmaceutical Review

MARCH 11, 2024

elaborated, noting that based on recall data collected by the US Food and Drug Administration (FDA) in over 100 products between 2000–2010, “fungi existed in 21 percent of products.” Ahmed et al. The authors also shared: “in the last three years [since 2023], the US FDA has recalled several drugs due to fungal contamination.”

Pharmaceutical 98

Pharmaceutical Food and Drug Administration Manufacturing Pharmaceutical products 98

Pharmaceutical Technology

JUNE 12, 2023

Currently, Jazz Pharmaceuticals’s nabiximols is the only cannabinoid approved for pain, receiving approval in Israel, in August 2010. In 2022, Pfizer acquired the drug, with the promise of accelerating clinical development via new, differentiated, and best-in-class approaches, enhancing optimism for further drug development.

Medical 143

Medical Prescription Management Manufacturing 143

Medical Device Success

DECEMBER 18, 2011

Getting from A to E www.medicaldevicesuccess.com/2010/11/18/getting-from-a-to-e/. Qualitative Benefits of Strategic Planning www.medicaldevicesuccess.com/2010/11/18/qualitative-benefits-of-strategic-planning/. Assumptions www.medicaldevicesuccess.com/2010/12/03/assumptions-–-defy-the-old-saying-that-results-in-“ass-u-me”/.

Medical 100

Medical Sales Marketing Consulting 100

Clarivate

NOVEMBER 1, 2021

Between 1981 and 2010 Henk was a senior staff member at the Centre for Science and Technology Studies (CWTS) at Leiden University, still now a center of excellence in the field of bibliometrics. Perhaps nobody in the world knows the ISI databases better than Henk Moed.” Moed obtained a Ph.D.

Education 105

Education Government 105

PM360

MAY 15, 2023

After a developmental day of shadowing a pharma sales rep, the fire was lite and she joined the sales team never looking back, ultimately landing her a role at ConnectiveRx in 2010.

Sales 94

Sales Pharma sales reps Prescription Recruitment 94

Pharmaceutical Technology

MAY 17, 2023

In 2010, the US Food and Drug Administration approved Glassia for the same indication. “To ensure wide access to eligible patients, we are excited to partner with the IDEOGEN Group, a company focused on the commercialisation of speciality medicines for rare diseases across Europe.”

Marketing 52

Marketing Food and Drug Administration Specialization Food 52

European Pharmaceutical Review

JULY 28, 2023

Soriot continued, remarking on retiring Executive Vice President of Biopharmaceuticals R&D, Mene Pangalos’ success in “delivering a greater than five-fold improvement in productivity [since 2010 and]… overseeing the creation of the DISC – our new R&D Centre in Cambridge, UK ”.

Medicine 98

Medicine Patients Pharma Pharmaceutical 98

European Pharmaceutical Review

JULY 12, 2023

This news builds on the success of the MenAfriVac ® vaccine, which eliminated serogroup A meningococcal meningitis outbreaks from the meningitis belt after being introduced in 2010. “[We]

Government 98

Government Safety Manufacturing Pharmaceutical 98

Copyright Clearance Center

OCTOBER 1, 2022

Copyright Office from 1994-2010. Her vast knowledge of copyright law, and the diverse communities it serves, was the foundation for her leadership as Register of Copyrights and Director of the U.S. CCC was enormously honored to have Marybeth serve on our Board of Directors upon her retirement from public service.

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59

European Pharmaceutical Review

AUGUST 16, 2022

The Queen’s Award for Enterprise is the UK’s highest accolade for business success and recognises the strength of Quay Pharma’s export sales, which, according to SGS, have comprised at least 55 percent of its business since 2010. The enterprise also noted that in the last three years its overseas sales had more than doubled.

Pharma 97

Pharma Sales Manufacturing Pharmaceutical 97

European Pharmaceutical Review

JANUARY 31, 2023

billion in poorer countries access to full medicine portfolio… MPP has signed 34 licences for various health technologies and facilitated access to 30 billion doses of treatments since 2010. NEWS: Pfizer offers 1.2 These successes have helped to define its new strategy.

Medicine 105

Medicine Manufacturing Healthcare Healthcare 105

European Pharmaceutical Review

AUGUST 23, 2022

A study of the causes of warning letters issued by the US Food and Drug Administration (FDA)’s Center for Drug Evaluation and Research (CDER) and Center for Devices and Radiological Health (CDRH) between 2010 and 2020 revealed that poor current good manufacturing practice (cGMP) compliance and misbranding were the most common citations.

FDA 105

FDA Food and Drug Administration Pharma Pharmaceutical manufacturing 105

World of DTC Marketing

JANUARY 14, 2022

The average time it takes to fill an open position is 44 days, representing a 50-percent increase since 2010. If you know what kind of profile you’re searching for, go for it and contact the best candidates immediately. Each day a job goes unfilled, the organization loses productivity as the position’s tasks remain undone.

Pharma 277

Pharma Recruitment Food Marketing 277

Clarivate

APRIL 24, 2024

We provided an early grant to non-profit Impactstory (now OurResearch), and as a founding sponsor of ORCID in 2010/11, we donated the foundational code from ResearcherID, to get it off the ground.

Government 103

Government 103

European Pharmaceutical Review

JULY 7, 2022

He then had a one-year stint at Merck Research Laboratories as Director of Clinical Research for Clinical Hepatology before returning to Bristol Myers-Squibb from 2010-2015. Dr Hughes earned his MD and PhD at Yale School of Medicine.

Medical 98

Medical Medicine Pharmaceutical Leads 98

Pharmaceutical Technology

APRIL 27, 2023

Sanofi markets avalglucosidase alfa as Lumizyme in the US to treat LOPD since its approval in 2010. The treatment will go up against Sanofi’s Nexviazyme (avalglucosidase alfa-ngpt) which received an EC approval in June 2022, following a US Food and Drug Administration ( FDA) approval in August 2021.

Food and Drug Administration 52

Food and Drug Administration Food Marketing Medicine 52

pharmaphorum

JANUARY 24, 2023

Since 2010, the UK has fallen from 4th to 98th place in overall trade balance in pharmaceuticals, due to fierce global competition, according to the MMIP. Over the same period, similar countries – including Ireland, France, and Germany – have been moving to boosting manufacturing productivity, output, and exports.

Manufacturing 108

Manufacturing Medicine Government Pharmaceutical manufacturing 108

Pharmaceutical Technology

SEPTEMBER 29, 2022

Comirnaty, the Covid-19 vaccine of Pfizer and BioNTech, is said to have infringed patents filed by Moderna between 2010 and 2016 for this technology. Cell & Gene Therapy coverage on Pharmaceutical Technology is supported by Cytiva. Editorial content is independently produced and follows the highest standards of journalistic integrity.

Pharmaceutical 59

Pharmaceutical Medicine Marketing 59

European Pharmaceutical Review

DECEMBER 14, 2023

EMA/95098/2010. The European Network of Centres for Pharmacoepidemiology and Pharmacovigilance (ENCePP). Guide on Methodological Standards in Pharmacoepidemiology (Revision 11). Internet] European Medicines Agency. cited Dec2023]. Available from: [link] Implementation of the pharmacovigilance legislation 2011 [updated 18 May 2015].

Medicine 116

Medicine Safety Competition Networking 116

World of DTC Marketing

JUNE 4, 2021

By 2010, it was up to 300 calories a day. In 2010, 15.1% So many of the additional calories in our diet that weren’t there a few decades ago are coming in the form of sugar. Back in 1977, the average adult got 228 calories per day from sugar in food and drinks. Added sugar consumption increased almost as much — 20 percent — among kids.

Food 207

Food Insurance Leads Medical 207

pharmaphorum

JULY 6, 2022

A new cross-sectional study has found that the FDA green lit 95% of the 89 new oncology therapies approved between 2010 and 2019 before the EMA, with the Europeans trailing the Americans by a median of 241 days. But while the figures may sound stark, they come as no surprise to the industry.

Safety 95

Safety FDA Medicine Patients 95

Pharma Marketing Network

APRIL 27, 2021

For more than twenty years, Susan has been a dedicated HBA volunteer serving on the global board of directors, including as President of the Global Board in 2010. Having also served on HBA’s Advisory Board, Council of Chapter Presidents and as a mentor to the European Chapter and numerous U.S.

Physicians 52

Physicians Networking Pharma Healthcare 52

European Pharmaceutical Review

MARCH 15, 2023

The second generation of MZmine, released in 2010, could process hundreds of samples over several days. Previous versions of MZmine The first version of MZmine has enabled scientists to automate the processing of datasets generated by analytical devices at an unprecedented scale.

Distribution 139

Distribution Networking Manufacturing Medicine 139

World of DTC Marketing

APRIL 7, 2021

Food and Drug Administration between 2010 and 2016 yet did taxpayers receive any discount? drug spending by 9 percent” What about taxpayers? Government funding contributed to research associated with all 210 new drugs approved by the U.S.

Healthcare 162

Healthcare Healthcare Food and Drug Administration Pharma 162

Clarivate

JUNE 6, 2024

Revealing global and regional insights In this report, we look at trademark filing and litigation trends since 2010 at six major trademark registers, the United States, the European Union, the United Kingdom, Mainland China, Japan and South Korea.

Specialization 64

Specialization Retail Engineering Marketing 64