Perficient: Drug Development

FEBRUARY 13, 2024

Learn about Adobe’s commitment to maintaining HIPAA-ready standards within commerce solutions and join Perficient and Adobe for a webinar hosted by CMSWire. EST Secure Digital Conversion: Unveiling Adobe’s HIPAA-Ready Commerce Solution webinar hosted by CMSWire. Register Today! Thursday, February 22 at 12:00 P.M.

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Pharmacy Science Regulations Marketing 52

The Pharma Data

MAY 5, 2021

FDA officials said that the number of a product specific guidances (PSGs) issued by the Office of Generic Drugs (OGD) has increased steadily since FY 2013. FDA webinar on product specific guidance for generic drugs . © 2021 Regulatory Affairs Professionals Society. Source link.

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The Pharma Data

SEPTEMBER 15, 2020

Find out solutions to mitigate the impact from clinical supply chain risk and discover how to improve dynamic drug supply forecasting strategies. Join this webinar to learn how supply forecasting and interactive response technology can help biotech companies improve supply planning and distribution while reducing cost and risk.

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Clinical Supply Clinical Trials Doctors Clinical Development 52

LifeSciVC

FEBRUARY 27, 2024

By Ivana Magovčević-Liebisch, CEO of Vigil Neuroscience, as part of the From The Trenches feature of LifeSciVC Patients and their care partners are at the center of our work in the life sciences industry – but at what point during the drug development process should companies start to engage these key stakeholders?

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Drug Development Disease Drugs Treatment 60

Perficient: Drug Development

SEPTEMBER 1, 2023

Register for this free webinar here We understand how to get the most out of Optimizely’s diverse digital experience platform to create highly effective and personalized experiences for our customers.

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Alta Sciences

APRIL 17, 2024

Five Promising Treatment Areas in Early-Phase Drug Development in 2024 aasimakopoulos Wed, 04/17/2024 - 15:52 Early-phase drug development is an ever-changing landscape, as emerging science leads to new promising areas of research for the treatment of human health issues.

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Drug Development Treatment FDA Approval Therapies 52

Alta Sciences

JUNE 9, 2023

Accelerating Global Drug Development Timelines With Ethnobridging rmaloney Mon, 06/12/2023 - 16:07 HTML Safe Strategy to Save Time and Money Avoid repeating Phase I studies for drugs intended for the Asian market. Download your copy today. In this complimentary webinar , Mel B. Watch the webinar.

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Drug Development Clinical Trials Biosimilars Pharmacokinetics 40

Alta Sciences

JANUARY 22, 2024

Get a Head Start On Your 2024 Preclinical Drug Development Program blussier Mon, 01/22/2024 - 15:18 HTML EXPERTISE Matters. With four strategically placed preclinical research facilities throughout North America, Altasciences can get your CTA/IND-enabling studies underway in just 8 weeks!

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Perficient: Drug Development

OCTOBER 27, 2023

The webinar covered three pivotal aspects: Seamless Migration, Future-Ready Strategies, and the PWA Revolution. Seamless Migration: Composable Storefronts and Accelerators The webinar initiated with a comprehensive exploration of seamless migration strategies. You can catch the entire webinar right here !

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Conversations in Drug Development Trends

FEBRUARY 22, 2023

Our rare disease team at Worldwide will be hosting a panel discussion webinar with patient advocates active in Rare Disease Day events to synthesize the most salient conversations taking place. See their conversation below and register for the webinar to hear more from these advocates!

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Disease Clinical Trials Trials Treatment 52

Conversations in Drug Development Trends

OCTOBER 26, 2022

Having worked in psychedelic research since the advent of industry-sponsored trials, Worldwide Clinical Trials has amassed the expertise needed to execute these studies successfully, recently sharing insights in a webinar titled “ Demystifying Complex Operations in Psychedelic Research ,” available on-demand now. Check out the full webinar !

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Trials Clinical Trials Licensing Licensing 97

Fierce BioTech

JULY 17, 2023

Best practices for capturing reproducible and accurate in vivo data to reduce failure in clinical trials – the most expensive phase of drug development. Discussion will include: Current in vivo study management practices and processes. How did we get here?

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Clinical Trials Drug Development Research Trials 88

Conversations in Drug Development Trends

JUNE 13, 2024

At Worldwide, Matt Cooper and Jim Eamma , our Executive Directors, Therapeutic Strategy Leads in Oncology, shed light on the intricacies of modern oncology trials in their recent webinar, “ Navigating the Landscape of Complex & Adaptive Oncology Trials.”

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Trials Clinical Trials Drug Development Clinical Development 52

Fierce BioTech

JANUARY 12, 2024

Developing and Manufacturing Minitablets to Extend Drug Lifecycle pesurya Fri, 01/12/2024 - 12:38 Wed, 02/28/2024 - 11:00 Resource Type Webinar Robert Strickley, PhD Valjon Demiri, MSc Duration 60 Minutes Oral minitablets can offer several advantages in pharmaceutical applications, making them a valuable option in drug delivery.

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Drugs Packaging Compliance Drug Development 52

Cytel

APRIL 3, 2024

Thank you to Charlotta Gauffin, Chief Scientific Officer at Dicot, for joining us for our recent webinar, “The Road to First-in-Human Trials: Insights from a Real-World Example.” Thoughtfully and carefully planned nonclinical studies help pave a smooth path toward first-in-human Phase 1 clinical trials.

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Clinical Trials Drugs Trials Drug Development 59

Alta Sciences

JULY 22, 2024

Insights in FIH studies provide valuable information on potential dosing, efficacy, and safety, and serve as a good guide for the regulatory requirements needed throughout clinical development. jpg Tags Clinical Trials Weight 1

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Trials Clinical Trials Clinical Development Clinical Research 52

Fierce BioTech

APRIL 10, 2024

Redefining Antibody Specificity Profiling for IND swheeler Wed, 04/10/2024 - 17:56 Thu, 06/06/2024 - 11:00 Resource Type Webinar Kris Raghavan, PhD Fernanda I. Staquicini, PhD Duration 60 minutes Assessment of antibody off-target reactivity is a regulatory requirement for clinical development. So, what are the alternatives?

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Perficient: Drug Development

OCTOBER 24, 2024

In our recent webinar, “Enhancing Trust in Healthcare,” experts David Allen and Michael Porter , along with Appian ’s Matt Collins, addressed the concerning decline in consumer trust within the healthcare sector. Watch the Full Webinar Now: Explore our award-winning technology partners , mentions by analysts.

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Compliance 52

Fierce BioTech

APRIL 4, 2024

Discover how leading organizations leverage AI to revolutionize operations and expedite drug development, ensuring faster access to life-saving treatments. Join our webinar: AI Advancements in Life Sciences: Accelerating Innovation. Click here to login. Listing Image Appian-LogoListing-9142023.png Register now!

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Science Compliance Drug Development Treatment 52

Perficient: Drug Development

AUGUST 3, 2023

Join us to learn how Perficient, a global digital consultancy with 7,500+ employees, is modernizing HR functions and enhancing the employee experience while better supporting our business by migrating from Oracle E-Business Suite to Oracle Cloud HCM.

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Fierce BioTech

MARCH 12, 2024

For biopharma and biotech companies, FSP partnerships have emerged as a pivotal strategy for accessing the complementary expertise and resource flexibility they need to meet their timelines, and innovative providers are implementing new, globalized FSP strategies to keep their clients ahead of the curve.

Clinical Research 52

Clinical Research Drug Development Trials Research 52

Fierce BioTech

OCTOBER 26, 2023

Are Gaps in Your Clinical Pharmacology Program Jeopardizing Your Drug’s Approval? pesurya Thu, 10/26/2023 - 14:05 Tue, 12/05/2023 - 11:00 Resource Type Webinar Julie Bullock, PharmD Krithika Shetty, PhD Blaire Osborn, Ph.D.

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Clinical Pharmacology Drug Development Regulations FDA 52

Fierce BioTech

MARCH 5, 2024

Click here to login.

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Drug Development Disease Research Drugs 52

Fierce BioTech

SEPTEMBER 6, 2023

Organofluorine Chem in Pharma Intermediates & APIs swheeler Wed, 09/06/2023 - 12:54 Wed, 10/18/2023 - 11:00 Resource Type Webinar Dr. Yuanqiang Li Dr. Pete Newsome Peter Halkjaer-Knudsen Duration 60 minutes Topics Covered: Introduction to Organofluorine Chemistry and its significance in pharmaceuticals. Click here to login.

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Pharmaceuticals Drug Development Drugs Research 52

Fierce BioTech

MAY 1, 2024

Join us on Monday, June 19, 2024 for one hour all about oral cyclic peptide drug development. png Listing Introduction Join us on Monday, June 19, 2024 for one hour all about oral cyclic peptide drug development. Smaller breakthroughs in our own labs demonstrate results worth registering for. Click here to login.

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Pharmacokinetics Drug Development Drugs 52

Fierce BioTech

MAY 1, 2024

png Listing Introduction Join us on Monday, June 19, 2024 for one hour all about oral cyclic peptide drug development. Logos Attribution 0 Attribution 0 Primary Category Biotech On Demand Off Enable Automatic On Demand On Registration Login Link Already registered? Click here to login. Listing Image BioDuro_ListingLogo_250x190.png

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Drugs Drug Development 52

Fierce BioTech

SEPTEMBER 13, 2024

Highlights From the Final ICH Drug Interactions Guideline pesurya Fri, 09/13/2024 - 11:39 Thu, 10/31/2024 - 11:00 Resource Type Webinar Brian Ogilvie Graham Dyck Duration 60 Minutes The ICH M12 Guideline was finalized on May 21st, 2024, after extensive review of industry and other comments.

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PPD

OCTOBER 16, 2023

Tokenization can accelerate innovation in clinical trials and drug development. Once in the data lake, tokenized data can be linked using a special linking software based on the data usage agreements to create longitudinal patient data. This enables deeper and more meaningful real-world insights on clinical study data.

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Clinical Trials Trials Research Therapies 98

The Pharma Data

SEPTEMBER 9, 2020

We respect your privacy, by clicking “Download Your Copy” you will receive our e-newsletter, including information on Podcasts, Webinars, event discounts, online learning opportunities and agree to our User Agreement. Develop a fully automated environment to significantly boost research efforts.

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Production Laboratories Compliance Government 52

Alta Sciences

AUGUST 7, 2024

blussier Wed, 08/07/2024 - 19:51 HTML Timing is Everything Early collaboration with an experienced CDMO is crucial in drug development to mitigate manufacturing risks and ensure the efficient formulation of your API for preclinical and clinical testing. Contact us today to discuss the next stage of your drug development journey.

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Clinical Trials Compliance Drug Development Trials 40

PPD

SEPTEMBER 16, 2024

The convergence of real-world data (RWD), technology and artificial intelligence (AI) is playing a vital role in accelerating drug development. In a recent panel discussion at DIA Global , our experts explored how these elements are reshaping clinical research and drug discovery.

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Clinical Development Clinical Trials Clinical Research Trials 52

Conversations in Drug Development Trends

AUGUST 10, 2023

For more information on how we ensure diverse and equitable trials, check out our webinar , where our Global Head of Regulatory Strategy, Aman Khera , discusses the importance of diversity and inclusion in clinical research and how to overcome potential obstacles through collaboration.

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Alta Sciences

JANUARY 24, 2024

Altasciences has conducted over 13,000 simulated drives in support of drug development. Download Listen You may also be interested in the following: • Driving Studies Webpage • Driving Studies Webinar Image Resource-Center_e-bulletin_The_Altascientist_issue_1-Driving_Simulation_0.jpg

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Clinical Trials Trials FDA Drug Development 40

Fierce BioTech

JULY 27, 2023

Process Chemistry Unleashed: A 'Fit-for-Purpose' Approach to Accelerate IND Filing pesurya Thu, 07/27/2023 - 11:27 Tue, 09/05/2023 - 10:00 Resource Type Webinar Qixuan Lu Duration 60 Minutes Process chemistry plays a pivotal role in various stages of the pharmaceutical R&D cycle.

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Process Chemistry Compliance FDA Drug Development 52

Alta Sciences

SEPTEMBER 5, 2024

The groundbreaking data also supports the use of the Sinclair Nanopig™ to reduce reliance on traditional non-rodent models in drug development. Read it now! ​​​​​​ WHITE PAPER Questions? Consult with one of our experts.

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Drug Development Drugs Research 40

Alta Sciences

NOVEMBER 20, 2024

EXPLORE Related resources you may be interested in: eBook: Nonclinical Studies in Cell and Gene Therapy Webinar: Best Practices to Reduce Animal Use in Toxicology Studies Webpage: The Use of Miniature Swine in Preclinical Studies Image alta-blog_4_2.jpg jpg Tags Preclinical Research Weight 1

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Perficient: Drug Development

DECEMBER 20, 2024

Discussion will include: Challenges with the legacy environment On-premises to cloud migration approach Benefits realized with the global SCM implementation Save the date for this insightful webinar taking place January 22, 2025! Register now !

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