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Therapeutics must demonstrate efficacy and safety to relevant regulatory authorities before they are approved for use in clinical practice. This is a relatively straightforward process, assuming the treatment positively impacts the relevant therapeutic area (e.g., ability to … Read More »
Pharmaceutical companies have historically resisted the shift to move beyond traditional representative-to-healthcare professional interactions. Prior to COVID-19 and before the days of abundant caution and social distancing, pharmaceutical sales teams were content with the … Read More »
It has never been more important to get your product launch strategy right. Increased competition, pressure on margins, and shorter time-in-market has placed enormous pressure on brand managers to craft a sound launch strategy and ensure it stays on track. With so much at st … Read More »
Recently, Brittany Erana, MPM, Vice President of PPD® Digital; and Niklas Morton, MSc, Senior Vice President of PPD® Digital, spoke with leaders of Science 37, Medable, and Takeda in an online forum about how the industry is shifting to focus on decentralized trials. They th … Read More »
Provided by Elligo Health Research Clinical research faces a dilemma that has historically plagued the industry: the lack of diversity in research. The underrepresentation of different races, genders, and classes is largely due to the fact that most trials exclusively enroll … Read More »
Learn more about the detailed patient points and associated physician data available from OffTheShelf. View our infographic. http://bit.ly/evidera-offtheshelf Highlights about OffTheShelf™: Understanding the market trends, market behavior, and competition when develop … Read More »
Amplity Health might be a name you’re still familiarizing yourself with, but you know them as the consolidation of their legacy family of brands – Tardis Medical, Touchpoint and PDI. Their new website pays tribute to where they’ve come from and the growth they’ve experienced … Read More »
Evidera’s multidisciplinary team of data scientists, epidemiologists, and statisticians offer a host of fit-for-purpose solutions to address your most challenging research questions. Learn more: http://bit.ly/RWEsolutions Offerings include: Database study designs Hybrid stud … Read More »
Relationships are built over time. However, with the inability to meet face-to-face, many life sciences commercial teams are left wondering what to do next. Unfortunately, we have been truly disrupted – not only in our work environment, but in what our customers, healthcare … Read More »
We’re implementing patient-centric approaches—like capturing real-world evidence from patient registries—to provide valuable information that can help you optimize your clinical research efforts. At Parexel, we’re changing what’s possible today for tomorrow. Watch our video … Read More »
This recent webinar covers a new model for planning trials, which will be illustrated through several case studies. The on-demand recording is now available. Overview During the COVID-19 pandemic, clinical trials of potential vaccines or treatments need to find study sites i … Read More »
In the first two blog posts in this series, we summarized aspects of our e-book covering the various options for automating safety case processing. With these technologies as they exist today, companies are able to automate a manual workflow. This includes everything from in … Read More »
Our first blog post in this series summarized two approaches to automating routine aspects of safety case processing. In this installment, we’ll review how various aspects of artificial intelligence (AI) can dramatically improve the process and make companies not only more e … Read More »
We’re looking for participants for an industry survey sponsored by Oracle Health Sciences. As a life sciences professional, your input is invaluable to this research project. Genomics, AI, IoT, and other new initiatives have the opportunity to revolutionize multivigilance. P … Read More »
With more companies responding to growing caseloads by using automation to streamline elements of the pharmacovigilance/multivigilance process, it’s useful for safety professionals to understand the different options available, as well as how automation today can eventually … Read More »
Sponsored by Parexel A successful FSP outsourcing model provides flexibility, control & access to a workforce with highly specialized skills & knowledge. It’s essential to evaluate & match the skill set & cultural fit of the candidate & sponsor. The Parex … Read More »
We’re looking for participants for an industry survey sponsored by Oracle Health Sciences. Genomics, AI, IoT, and other new initiatives have the opportunity to revolutionize multivigilance. Please answer this short, anonymous survey and add your voice to this key industry re … Read More »
Click here to download printable PDF The Coronavirus Treatment Acceleration Program (CTAP) is a special emergency program instituted by the US Food and Drug Administration (FDA) in response to the COVID-19 pandemic The primary goal of the program is to expedite the availabil … Read More »
Sponsored by Covance Watch now Technology is often touted as a silver bullet, but often the promise falls short of the unrealistic expectation of a tech driven utopia. Knowing when to deploy which technologies requires a pragmatism that balances technology with people and pr … Read More »
Sponsored by Covance Register The PMSR regulations for drugs, devices, and biological products share many similarities, each set of regulations establishes distinct reporting requirements, including reporting triggers and timeframes. In this virtual webinar, expert panelists … Read More »
