Search results for Pharo Studio

Mednet is a healthcare technology company specializing in eClinical solutions designed for the global life sciences community. Pharmaceutical, medical device, biotechnology and Contract Research Organizations (CROs) around the world have trusted Mednet for over 23 years to deliver the technology innovation, experience and reliability they need for success. Mednet’s comprehensive, EDC-centric eClinical platform, iMednet, optimizes clinical studies of all types and sizes – accelerating research with exceptional flexibility, ease-of-use, robust functionality, affordability, and stellar support. iMednet is feature-rich and uniquely designed to help sponsors and CROs get studies up and running quickly and to see them through with a full suite of native capabilities, including: randomization, trial supply management, adjudication, ePRO, payments, DICOM Imaging, and eConsent. All backed by a highly tenured and experienced support team, ensuring quality, compliance and easy onboarding of the entire research team and clinical trials sites.

Brandcrush is unlocking the media potential of businesses globally with a simple but powerful platform that makes it easier to buy and sell shopper marketing, retail media and partnerships. We power retailers and broader businesses to transform their in-store media, out-of-store media and brand partnerships from antiquated PDF packs and spreadsheet management to a scalable solution that the worlds’ leading brands and agencies trust. Our software enables our partners to unlock and grow their media revenue without having to grow their team with self-serve media portals, outbound sales tools, smart inventory and workflow management solutions. Our core clients include grocery & pharmacy retailers, shopping centers, direct to consumer meal Kit businesses, gyms & yoga studios, Universities, media agencies and FMCG Brands.

Evalus AI is an eClinical platform built by TatvaCare for pharma sponsors and contract research organisations running late-phase trials, post-marketing studies and real-world evidence programs. The platform covers electronic data capture (EDC), clinical trial management (CTMS), randomisation and trial supply (IWRS), electronic trial master file (eTMF) and survey studies. Teams can deploy the full platform or a single module such as EDC. AI is built into Evalus AI EDC. Site staff can enter data by voice, and uploaded source documents are read with OCR, which cuts manual transcription. Every module includes a full audit trail, electronic signatures and role-based access. The platform is hosted on Microsoft Azure in India and integrates with EMR and HMIS systems, lab systems and safety databases, with CDISC SDTM and ODM exports and APIs. Studies typically go live within a week of contract.

BrawoAI is a review collection tool for small service businesses in Poland that want a simple, organized and compliant way to collect real Google reviews. After a completed service, the owner or staff member enters the customer phone number in the mobile app, web dashboard or Apple Watch companion. BrawoAI sends an SMS with a link. A happy customer can continue to Google Reviews, while an unhappy customer can first send private feedback to the business. The system turns review requests into a repeatable process instead of leaving them to chance. The dashboard shows request history, SMS limits, new reviews, private feedback and AI-assisted reply drafts. A business can react faster to difficult signals, while satisfied customers get a clear path to leave a public review. BrawoAI does not sell reviews, remove negative reviews or impersonate customers. It is not a fake review agency; it is an operational workflow for the moment after service delivery. BrawoAI is built for hair salons, beauty studios, workshops, driving schools, restaurants, pharmacies, dentists, physiotherapists and other service businesses. The free plan includes 25 SMS requests or 5 new reviews from business registration. Paid plans start at PLN 99 per month and scale with SMS request volume.

Studylog is in-vivo study management software used by pharmaceutical companies, biotech firms, contract research organizations (CROs), and academic research institutions to manage the workflow of in-vivo research studies. The platform covers the study lifecycle from design through reporting, including study design and scheduling, task and measurement tracking, data acquisition, randomization, data analysis, and report generation. The software is used to replace spreadsheet-based tracking methods with a centralized database that stores study data, protocols, and results in a single system. Data can be entered manually or collected automatically through integrations with wired and wireless scales, calipers, and blood analyzers. Studylog also integrates with GraphPad Prism for graphing and statistical analysis, and supports bioluminescence imaging (BLI) data. Key functionality includes: - Study design tools, including reusable study templates and the ability to clone prior studies for follow-up research - Task and measurement scheduling with timers and completion tracking - Multiple randomization methods (stratified, matched distribution, multi-parameter, and pure random), with options to randomize by parameters such as age, body weight, or tumor volume - Automated data collection from connected laboratory devices - Built-in graphing, including box plots, group mean line graphs, and Kaplan-Meier survival curves - A calendar view for scheduling and tracking tasks across multiple concurrent studies - Standardized dictionaries and nomenclature for consistent data entry across studies - Access controls and permissions by user, team, and study - A web API for integration with electronic lab notebooks (ELNs) and other systems Studylog is offered as a desktop application and includes offline access, allowing users to continue working with synchronized study data when network connectivity is unavailable. The company has provided in-vivo study management software for more than 20 years and offers customer support staffed by former in-vivo researchers.

We develop pharma-tailored solutions to extract evidence from various data sources, including CRM systems, social media, job advertisements, clinical studies and other external data providers.

OnlineCRF is a cloud-based Electronic Data Capture system designed to streamline data collection and management in clinical trials, post-marketing studies, and registries. Tailored to meet the specific requirements of each study protocol, OnlineCRF offers a user-friendly interface that facilitates efficient data entry and real-time monitoring. The system is fully compliant with industry standards such as FDA 21 CFR Part 11, GCDMP, and GDPR, ensuring data integrity and regulatory adherence. Key Features and Functionality: - Data Pre-Validation: Ensures that only valid data within specified ranges are saved, reducing errors during data entry. - AE/SAE Reporting: Facilitates adverse event reporting with automated notifications to the pharmacovigilance department. - Query Generation: Allows Clinical Research Associates to generate and resolve queries for questionable data, enhancing data accuracy. - Randomization: Supports various randomization methods configurable before data collection begins. - Audit Trail: Maintains a comprehensive record of all data modifications, including reasons and user details, ensuring transparency. - Digital Signature: Enables principal investigators to electronically sign completed and verified Case Report Forms . - Real-Time Monitoring: Provides dashboards for tracking study progress and investigator activity, allowing for immediate corrective actions if needed. - Multilevel Backup: Implements data backups every two hours, storing multiple copies on physically separated servers to ensure data security. Primary Value and User Solutions: OnlineCRF addresses the complexities of clinical data management by offering a comprehensive, secure, and compliant platform that enhances data quality and operational efficiency. Its intuitive design reduces training time, allowing research teams to focus on their core activities. The system's flexibility accommodates various study designs, including randomized and non-randomized trials, as well as single or multi-country studies. By providing real-time monitoring and robust data validation, OnlineCRF ensures that clinical trials remain on track, facilitating faster and more reliable research outcomes.

Qualified Controls provides regulated environmental monitoring and mapping as one service, for refrigerators, freezers, ultra-low freezers, incubators, cleanrooms, cold rooms and warehouses. Monitoring: wireless sensors report continuously to a cloud platform with live dashboards and floor-plan views. Alarms go out by SMS, voice, email and mobile push, escalating by severity, zone and on-call schedule. Every reading, alarm, acknowledgement and configuration change is kept in a tamper-evident audit trail with electronic signatures, aligned with 21 CFR Part 11 and ALCOA+. Mapping and validation: mapping studies capture loaded, unloaded and recovery profiles to find hot and cold spots. The result is a signed report and a permanent sensor-placement plan. We author and execute IQ/OQ/PQ protocols. Calibration: NIST-traceable calibration, performed onsite and ISO 17025 accredited laboratories. With Hot-Swap service, pre-calibrated replacement sensors are swapped on site, so monitoring never stops. Built for pharma, biotech, hospital pharmacy, blood banks, biobanks, laboratories, CDMO, cold-chain logistics, and food operations.

KAI Conversations gives pharmaceutical companies visibility into their most valuable and least captured data: what actually happens in field conversations with healthcare professionals. Reps and MSLs record calls through the mobile app, Zoom or Teams, and KAI's AI analyses each one, scoring the strength of connection with NetKonnector, a behavioural science measure across 12 dimensions that predicts belief shift and outcomes. Every conversation produces value at three levels. Reps get Game Tape analysis, personalised coaching nudges, auto-populated CRM summaries and next-call prep. Managers and marketers get a shared view of message delivery, HCP reception, objections and field capability gaps. Franchise and country leadership get strategic HCP, clinical and competitor insight from real conversations, a faster, richer alternative to surveys and ATU studies that report claimed behaviour rather than what was said in the room. The result: more effective coaching with less admin, marketing decisions grounded in real HCP evidence, and time to insight collapsing from quarters to days. KAI works across commercial and medical teams, brands, therapy areas and markets.

Cinnamon Entertainment Group LLC was founded by President Rob Salerno in September 1998 and is the holding company for 3 businesses: Digital Media Nashville and New York digital marketing consulting, SimpleVerse Artist Management and Website Publishing. Our brands consist of NJJobMarket, MobileWirelessJobs, BioTechPharmJobs, CliquePrize and DreamBackfield. In 2018, we became accredited by the Better Business Bureau – Nashville. You can also find more information at Dun & Bradstreet. We offer SEO and other digital marketing services for Arts & Entertainment companies such as art galleries, artists (Musicians, Bands, Singers, etc), photographers, record labels, music, dance studios, music schools, piano stores,

Aleph Alpha is a German artificial intelligence company specializing in developing sovereign AI solutions tailored for enterprises and governmental agencies. Founded in 2019, the company focuses on creating large language models (LLMs) and multimodal AI capabilities that integrate both text and image data. Their flagship product, PhariaAI, is a comprehensive generative AI suite designed to assist organizations in designing and managing bespoke AI use cases. Key Features and Functionality: - PhariaAssistant: Enhances productivity for knowledge workers by summarizing text, extracting information from documents, and translating content. - PhariaStudio: Provides a unified workspace for developing, debugging, fine-tuning, and evaluating AI models and applications. - PhariaOS: Manages access to AI resources, enabling IT administrators to monitor installations and resource availability. - PhariaCatch (Upcoming): Will integrate with other components to gather structured feedback from subject matter experts, ensuring continuous improvement of AI applications. Primary Value and Solutions: Aleph Alpha's solutions address complex and critical business challenges by providing: - Sovereignty: Empowering organizations to build and retain their own competencies, protect data and intellectual property, and operate without vendor lock-in. - Transparency and Compliance: Offering AI explainability and transparency, crucial for meeting internal and external regulatory requirements. - Future-Proofing: Ensuring that investments in AI specialization and integration remain relevant as technology evolves. - Human-Machine Collaboration: Providing tools that allow experts to maintain control and responsibility in complex environments where traditional chatbots may fall short. By focusing on these areas, Aleph Alpha enables enterprises and governments to harness advanced AI technologies while maintaining control, compliance, and adaptability in an ever-changing digital landscape.

EXTROVERT | Business Communications is an independent corporate Public Relations agency based in Athens, Greece. EXTROVERT provides premium services across different fields of communications and delivers high-impact PR strategies and campaigns for leading international and local companies and organizations in the technology, maritime, cruising,healthcare and pharma and B2B sectors. We pride ourselves for being a trusted PR agency and a strategic partner, always looking for new opportunities and creative ways to deliver value to our clients’ business and support their growth. Our services include: _Communications Consulting _Marketing Communications _Press Office & Media Relations  _Digital and Social PR _Events Management & Exhibitions _Associations Management _Science Communications _Creative Studio  Our leverage is our people. The EXTROVERT team consists of experienced professionals in the communication sector with excellent knowledge of the market. We have original ideas, a great deal of creativity and dedication. We view communication as a whole and approach it from different angles: as executives, as consultants, as consumers. We monitor the market, identify with your needs and listen to your concerns.    Above all: we deliver.                                                        

Lorenzo Gutierrez, digital marketing consultant and strategist at Lorenzo Gutierrez Digital Marketing, a digital marketing agency with offices in San Francisco and Los Angeles, California.Lorenzo Gutierrez has a Master’s in Business Strategy and Management from University of Western Governors University class of 2013.He has been strategically designing and executing SEO and digital marketing projects since 2008.Lorenzo has given conferences, workshops, and courses about Google, SEO, digital marketing, and digital advertising since 2008.Lorenzo has 10 years of experience in entrepreneurship, strategy, business, marketing, and sales; and 10 years of experience in digital marketing, consulting, strategy, SEO, and digital advertising. You can see the complete Lorenzo Bio at the following LinkedIn profile: Authoritativeness:Lorenzo has written and published over 100 articles about Google, SEO, digital marketing, and digital advertising. You can read Lorenzo’s articles at the following links: Lorenzo’s Blog, TheManifest, Hackernoon, Convert and Clicktotweet Our agency has been featured at Hubstaff, Clutch, and Top Design Firms as one of the top digital agencies in San Francisco and Los Angeles.Lorenzo is one of the top shared content marketing authors of 2019. Trustworthiness:We help businesses all over the nation, to grow their revenue online with results oriented digital marketing.Lorenzo is a certified Google partner you can view his certifications at the following link:Google Certifications Page. You can write me lorenzo@lorenzogutierrez.net or you can call me at (415) 851-5644 or (323) 329-5697 if you need our services. Lorenzo has worked for and with corporate brands such as Biochain Institute Inc and Novabay Pharmaceuticals. We have also worked for small and medium size companies. You can read our recent case studies at the following links: https://lorenzogutierrez.net/marketing-case-studies/ You can read recomendations at his LinkedIn profile or his testimonial page: https://www.linkedin.com/in/lorenzo-gutierrez-mba/ https://lorenzogutierrez.net/testimonials/

Powered by industry-leading ChemDraw® and Spotfire™, the Signals Research Suite delivers best-in-class analysis and data visualization for the Make-Test-Decide R&D life cycle, fostering rapid innovation in Pharma & Biotech and Chemicals & Materials. In Pharma & Biotech, the Suite is ideally suited for research use cases involving early and late-stage in vitro assays, cell line optimization, biologics process optimization, in vitro DMPK assays, animal pharmacokinetics studies, efficacy, and safety studies. And in Chemicals & Materials, the Suite empowers product development workflows by increasing productivity, helps to improve product performance by simplifying screening and optimization processes, and reduces product development timelines.

Open Influence is a global, award-winning creator marketing company dedicated to delivering comprehensive influencer marketing solutions across major social media platforms. With over 12 years of experience, Open Influence has successfully partnered with top brands in industries such as fashion, lifestyle, automotive, entertainment, technology, consumer packaged goods, and pharmaceuticals. Their proprietary platform boasts the industry's largest collection of influencer data, utilizing machine learning and image recognition to analyze more than 100 million pieces of content. Notable clients include Under Armour, Pepsi, Puma, Corona, Hyundai, Unilever, Samsung, McDonald's, Universal Studios, and Verizon. Key Features and Functionality: - Strategy & Creative Development: Crafts strategic, attention-grabbing campaign concepts that elevate creators’ creativity, delivering memorable and high-impact brand experiences. - Campaign Management: Provides seamless, end-to-end campaign execution, managing every stage with precision to ensure brand safety, quality assurance, and measurable impact across industries and platforms. - Paid Media Amplification: Employs a strategic paid media approach to ensure that creator content reaches the right audience at the right time, maximizing impact across every stage of the funnel. - Studio OI: Premium Content Production: Produces high-quality content that brings a brand’s story to life, managing creative development to post-production with top creators and celebrity talent for maximum impact. - Omnichannel Campaign Strategies: Develops innovative, multi-channel strategies, including out-of-home and experiential activations, to extend impact beyond social media and create seamless, high-impact brand experiences that drive deeper engagement. Primary Value and Solutions: Open Influence addresses the challenge brands face in effectively engaging and growing their desired audiences through social media. By offering a full suite of creator marketing services under one roof, they streamline the process of influencer collaboration, ensuring brand safety, quality content, and measurable results. Their data-driven approach, leveraging AI and machine learning, enables smarter decision-making and effortless execution, leading to real, impactful outcomes for their clients.

WIZLO is a white-label telehealth platform for founders and operators launching, running, or expanding telehealth clinics. It connects patient intake, EMR, prescribing, provider workflows, pharmacy fulfillment, payments, and the patient portal in one platform. Teams can configure branded intake forms with conditional logic, manage charts and encounters, and follow prescriptions, orders, and payments through connected workflows. Patients use the clinic's branded portal for messages, documents, appointments, subscriptions, and refill requests. WIZLO supports an end-to-end setup through Wizlo Launch Studio and scoped Enterprise Integration for businesses connecting existing systems. Clinics can use their own clinicians, access the WizDoc provider network, or combine both, and choose products and fulfillment partners from the available pharmacy network. Treatment availability varies by state and program. Wizlo Pay connects payment collection with clinic operations. Available capabilities and integrations depend on the selected implementation and commercial arrangement. Operators can book a discovery call to evaluate fit, onboarding, migration, and pricing for their business.

DDReg Pharma, a Global Regulatory Solutions and Safety Services organization is based out of Delaware in the US. The delivery of services currently happens from their India offices. They have a presence in Mumbai, Hyderabad, and Gurgaon. Incepted in the year 2009, the company is involved in a wide variety of regulatory & drug safety assignments across global markets. Rich subject matter expertise is combined with cutting-edge technology solutions providing end-to-end support across the pharma value chain. The company supports global pharmaceutical organizations in their needs to address regulatory challenges regarding Biologicals, Complex formulations, INDs, NDAs and Generics, Consumer Healthcare Products, and Medical Devices, in highly regulated markets as well as in complex emerging markets. The services portfolio includes Document management, Dossier support, pre-Approval, and Post MA regulatory support, Submission management, Regulatory Intelligence, Regulatory Strategies, Feasibility Studies, Dossier compilation, submissions, Agency follow-ups, and approvals. The Drug Safety Vertical supports global organizations in managing their worldwide Safety Obligations by way of Case Management, Aggregate Reporting, Safety Compliances, Signal Detection, and Risk Management. Functional and Operational Excellence are manifested through Strong Quality Management System and Efficient Project Management.

Akkure Genomics is at the forefront of integrating Artificial Intelligence (AI) and genomics to revolutionize cancer clinical trial recruitment. By analyzing patients' unique genetic profiles, Akkure's platform precisely matches individuals to suitable clinical trials, enhancing the development of personalized and effective treatments. This patient-centric approach not only accelerates the recruitment process but also increases the likelihood of trial success, benefiting both patients and pharmaceutical companies. Key Features and Functionality: - AI and Genomic Trial Matching: Utilizes advanced algorithms to assess patients' genomic data, identifying clinical trials that align with their specific genetic makeup. - Cancer Trial Recruitment: Streamlines the enrollment process by efficiently connecting eligible patients with appropriate trials, reducing manual screening efforts. - Support for Charities and Pharmacies: Offers an AI-powered Cancer Trials Finder that can be seamlessly integrated into charity or pharmacy websites, enhancing user engagement and providing personalized trial recommendations. - Enterprise Solutions for Hospitals: Transforms hospital clinical trial processes into high-efficiency centers by providing swift insights into patient populations and mitigating the risk of unsuccessful studies. Primary Value and Problem Solved: Akkure Genomics addresses the critical challenge of matching patients to suitable cancer clinical trials, a process often hindered by complex eligibility criteria and manual screening. By leveraging AI and genomic data, Akkure enhances the precision and efficiency of this matching process, leading to faster patient enrollment, reduced costs for pharmaceutical companies, and improved patient outcomes through personalized treatment options. This innovative approach accelerates the discovery of new therapeutics and brings us closer to a future where every patient receives treatment tailored to their genetic profile.

Zometric Continuous Process Verification & APQR is built for regulated pharmaceutical manufacturing, automating the two most resource-intensive compliance activities in the plant. The Annual Product Quality Review stops being a months-long sprint and becomes a living document the inspector can open today. Compliance becomes the byproduct of doing the work, not a separate deliverable. What changes versus the traditional APQR process: * Data collection: manual consolidation from paper and spreadsheets, arriving months after the campaign, is replaced by automated real-time streaming from instruments, MES and Zometric Edge. The data is in the dashboard before the batch is released * Analysis: offline statistical studies with limited visibility are replaced by live control charts and capability statistics. CPV becomes a state you observe, not a study you run once a quarter * Reporting: the static, hard-to-verify annual PDF becomes a dynamic living document that updates as the process runs, always traceable to the underlying records * Storage: high-cost paper archives kept for years are replaced by searchable digital storage. Retrieval that took weeks now takes seconds, with full lineage to the source measurement Compliance architecture: * 21 CFR Part 11 electronic signatures on every action * Complete user-action audit trail per record * Anytime inspection readiness: when the inspector arrives, you do not prepare, you open the dashboard. Every record, every signature, every trend is one click away Built for the standards your regulators already require: US FDA 21 CFR Part 11, ICH Q10, US FDA cGMP, ISO 13485 and 21 CFR 820, extending coverage to medical device quality systems. Analysis runs on the same validated Statistical AI engine behind the Zometric platform, including ICH Q1E compliant stability studies. Deployed at pharmaceutical manufacturers including Brawn Laboratories, Extrovis and Sekhmet Pharmaventures group companies. Browser-based, deployable cloud, hybrid or on-premise. Free pilot configurable in 2 to 3 weeks with your real data.

Electronic Data Capture software streamlines the gathering of trial patient data for early to late-stage clinical research phases, as well as post-approval studies. An adaptable and scalable EDC system is used by Pharma, Biopharma, Medical Device Companies, across the clinical research industry.