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PPD, Clinical Ink join on lupus assessment and endpoint data

PPD, Clinical Ink join on lupus assessment and endpoint data The two companies have partnered to develop a systemic erythematosus assessment review to streamline clinical trials centered on the autoimmune disease. Global contract research organization (CRO) PPD has collaborated with clinical technology firm Clinical Ink to develop a systemic lupus erythematosus (SLE) assessment review process that is intended to simplify the operation of clinical trials for the autoimmune disease. According to the companies, the collaborative approach is focused in enhancing data quality, as well as improving site staff experiences and inefficiencies, to help develop novel SLE therapies. Carol Olson, senior vice president and head of global product development with PPD, told Outsourcing-Pharma that trials involving SLE can be especially complex, particularly regarding assessments and endpoints.

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What s new in ePRO, the customer service behind it, and how you can benefit

What s new in ePRO, the customer service behind it, and how you can benefit
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Introduction to eLAS®

Introduction to eLAS® Clinical Ink has developed a unique offering the electronic Lupus Assessment Suite (eLAS ®) to address fundamental challenges impacting systemic lupus erythematosus (SLE) studies and the integrity of the study endpoints. eLAS is a therapeutic-specific application of Clinical Ink’s Lunexis™. Unlike other applications that simply offer stand-alone electronic versions of questionnaires, eLAS features a fully integrated suite of SLE disease assessment questionnaires, physical assessment, tender/swollen joint count, PGA, and summary forms. Latest content from Clinical Ink Content provided by Clinical Ink

Product brochureLupus assessment suiteClinical inkData managementPhasei iiPhase iii ivப்ராடக்ட் சிற்றேடுலூபஸ் மதிப்பீடு தொகுப்புமருத்துவ மைதகவல்கள் மேலாண்மைகட்டம் ஈயீ இவ்

Global Virtual Clinical Trials Market 2020-2027 - Fear Among Clinical Investigators for COVID-19 Presents Opportunities

The global virtual clinical trials market size is expected to reach USD 13.78 billion by 2027 Virtual Clinical Trials (VCT) are a new method of directing clinical trials which is inclusive of web platforms (informed consent, recruitment, adverse reactions, counseling and measurement of endpoints) and taking advantage of technology such as monitoring devices, apps and others. VCT also allows participant to be home-based at all clinical trial stage. VCT are operationally feasible and have lower drop-out rates, higher recruitment rates, better compliance and are faster than traditional method. The growth of virtual clinical trials is mainly owing to the advantages offered by these trials in place of traditional clinical trials. The cost of development of a new drug estimates more than a 2 billion dollars and approximately two-third of the total cost is consumed in clinical testing phase.

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02 24 21 -- Insource, Outsource, Or Both? Choosing The Right Model For Your Clinical Workforce

02.24.21 Insource, Outsource, Or Both? Choosing The Right Model For Your Clinical Workforce Orphan drugs are notorious for their high costs and risk factors, which are attributed to smaller patient pools and higher development and launch costs. Attend this webinar to learn more about key trends that are causing the rise of orphan drug indications, fast-tracking early development phases that will lead to commercial success, and more! By Mark Shapiro, Pharma Initiatives While traditional full-service outsourcing is still prevalent (and practically required for small or virtual biotech companies), and some organizations continue to maintain permanent in-house clinical teams, many others especially midsize and larger organizations are increasingly taking advantage of other models.

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