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Professional Edition: Powerful Analysis & Reporting, Improve communication with prospects Powerful reporting capabilities with slice and dice reports, MIS and. EQMS 2014 Free Trial - Download, Install & get started, no registration or personal details needed. EQMS 2011 Professional Edition : A simplified Sales CRM EQMS 2011 CRM is smart,easy,affordable and ready to use Sales CRM to manage your sales leads. EQMS 2011 Professional Edition : A simplified Sales CRM EQMS 2011 CRM is smart,easy,affordable and ready to use Sales CRM to manage your sales leads. EQMS. From Spinso: EQMS Professional is simple ready to use sales CRM to maage your Enquiries/Leads in 3 easy steps Enquiry - Follow-up - Closure. Features.Spinso EQMS CRM 2. Free Trial : :3 Simple step to try EQMS Professional Edition. EQMS is a simple, ready to use Sales CRM software to manage your sales process. It covers sales process with 3 easy steps enquiry, follow- up & closure. It comes in various edition My, Basic, Standard, Professional, Premium, Enterprise & Custom to suit needs of individuals, small & medium business and corporates. With EQMS you can choose to store data on your pc/server or cloud, in both case you just pay monthly rental.EQMS Professional is simple ready to use sales CRM to maage your Enquiries/Leads in 3 easy steps Enquiry - Follow-up - Closure. Features. Download Eqms Software. EQMS Lite 2012:Free Sales CRM v.2012R1.0 EQMS Lite. Spinso EQMS 2011 Professional Edition v.2011R1.2 EQMS 2011 Professional Edition .Free download, review of EQMS Professional : CRM for SME 2012R 5.1 (Spinso). EQMS Professional CRM has all the required features to manage the sales lead effectively.EQMS is available for free trial hence we would recommend you to experience the product first hand. You can also install EQMS on LAN for trial use.. EQMS Lite : Free CRM Download. Downloading EQMS Lite : Free CRM 2025.1.0 EQMS Lite : Free CRM Download. Downloading EQMS Lite : Free CRM 2025.1.0

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SMARTSOLVE® EQMS FOR LIFESCIENCES Manage quality and regulatory compliance with an end-to-end, modular, scalable solution Increase productivity and reduce compliance risk with a commercially focused integrated eQMS/RIMS suite Audiogram Optimize processes with IQVIA SmartSolve eQMS Mike King, Senior Director of Product and Strategy, IQVIA, discusses how a company of any size can benefit from deploying an eQMS software solution built specifically for life sciences. Your Enterprise Quality Management System IQVIA SmartSolve eQMS for life sciences is an award-winning platform. It is your single source of truth to overcome regulatory challenges and manage the complexities of quality compliance.SmartSolve eQMS software has been designed to meet EU MDR, EU IVDR, US 21 CFR, and ISO 13485 requirements.Whether you need to enhance post-market surveillance or use digital tools for complaint management and adverse event reporting, IQVIA’s end-to-end eQMS can support your company throughout product life-cycle management. >1.1 Million users globally 26+ Million complaints managed 37+ Million certifications conducted Deliver real business impact IQVIA SmartSolve for Quality, IQVIA RIM Smart for Regulatory, and IQVIA Vigilance Platform for Safety are the only intelligently connected integrations of quality, regulatory, and safety processes designed specifically for life sciences.Automate a single process or optimize your entire quality management system to improve efficiency, accelerate regulatory approvals, and simplify global control. eBook Transform your workflow with IQVIA’s SmartSolve eQMS Learn how the modular and scalable SmartSolve eQMS enhances regulatory compliance and accelerates time to market by continuously improving quality processes. Industry Recognition 2024 Frost & Sullivan Award Winner F&S awards IQVIA with Best Practices Customer Value Leadership Award in the global artificial intelligence regulatory and quality solutions space for the healthcare industry. Read more. 2023 Frost & Sullivan Award Winner SmartSolve is recognized with Frost & Sullivan’s 2023 North American Enabling Technology Leadership Award in the QMS market for life sciences industry. Read more. Explore More The award-winning SmartSolve eQMS for MedTech and Pharmaceutical companies enhances quality and improves regulatory compliance, enabling organizations to deliver life-changing therapies to patients faster. Small and emerging biopharma can also be at the forefront of tech innovation by automating their quality compliance management with IQVIA SmartSolve Fundamentals. A cloud-based inventory management solution designed for small and large businesses. The tool digitizes inventory processes, offering transparency over assets such as IT equipment, tools, machines, production facilities and the vehicle fleet. The ...Read more about TimlyQualcy QMSQualcy eQMS application is simple and easy to use, designed for Bio-Med and Life Science industry requirements. This software helps maintain compliance readiness, and enables proactive problem solving with visual metrics and notifications. The Qualcy eQMS ...Read more about Qualcy QMSGAGEpackGAGEpack is a comprehensive calibration and statistical process control (SPC) analysis management solution, which assists manufacturing firms of all sizes with gage management and compliance. It is relied upon by manufacturers in a variety of industries, i...Read more about GAGEpackAsset InfinityAsset Infinity is a cloud-based asset management suite. The product is available on the web and mobile (Android and iOS). Asset tracking and management module offers features like location, department, employee wise tracking, documentation at check-in and...Read more about Asset InfinityCalibration ControlCalibration Control is a cloud-based solution designed to help businesses across various industry verticals such as healthcare, design engineering, metrology, mining, testing, aerospace, oil well, packaging, distribution and more manage preventative mainte...Read more about Calibration ControlAsset PandaAsset Panda is a cloud-based platform for facility managers that offers a suite of applications including asset tracking and maintenance management. It is compatible with Windows, Mac, iPad, iPhone and can be used from anywhere while updating data in real-...Read more about Asset PandaMomentum QMSLooking for a comprehensive eQMS that covers Document Control, Health & Safety,

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The most affordable eQMS software for agile, lean, founder-lead companies.For EU MDR and FDA compliance.For Software and Hardware devices.Watch The Quick WalkthroughWe're collaborating with BerlinCert, a Notified Body focused on Software as a Medical Device (SaMD), on data formats for audit submissions.Learn more here.What is it?Formwork is a cloud-based, GDPR-compliant eQMS software for medical device startups. Document review, versioning and archiving. Training and CAPA management. Technical documentation for your medical device. Risk management and usability data tracking. All you need to pass your audits, in one place.OK, what's the catch?There is no catch. We’re just a bunch of people who are tired of shady practices in the eQMS software space and medical compliance in general. We built Formwork to help startups like yours get their medical devices certified while being transparent and fair. We’re not here to lock you in or charge you a fortune for adding more than two users.Take a closer lookUse our templates and text editor to create your documents. Review and sign them with our built-in workflow.User-friendly way to manage the technical documentation for your medical device. Software or hardware, we support both!You get instant feedback regarding th completeness of your technical documentation.From Zero To Successful Audit.In 6 Months.akina, a startup focusing on Physiotherapy, passed their MDR QMS audit only 6 months after starting with Formwork:"OpenRegulatory's Formwork offers distinct advantages to startups embarking on their regulatory compliance journey. With its dual functionality encompassing both Quality Management System (QMS) and Technical Documentation capabilities, it has provided us with a holistic solution that streamlines our quality processes while enhancing the management of our technical documentation.One key aspect that stands out is the simplicity and user-friendliness of the interface and the added convenience of pre-built templates and a wizard tool, complemented by instructive tutorial videos, which supported us in establishing an ISO 13485 compliant and certified QMS. Another standout aspect of OpenRegulatory is their exceptional customer support. The team consistently demonstrates a commitment to addressing our inquiries promptly and providing assistance as needed. Their dedication to ensuring our satisfaction is truly commendable and makes us feel valued as customers.In conclusion, OpenRegulatory has proven to be an invaluable partner for startups embarking on their regulatory compliance journey."Isabella BauerQuality & Regulatory Affairs Manager at Akina LtdNoah Labs got their connected-care platform for cardiology certified as an MDR class IIa device:“With Formwork, we successfully set up our quality management system and also

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Yourself and it takes a few minutes. You’ll have to put in some work actually integrating this data into your new system, of course. Contrast this with other eQMS providers which don’t even provide a data export like we do.Why is Formwork less expensive than other compliance software?Other manufacturers have huge sales teams. We just have our website. Other manufacturers target large enterprise companies. We target startups and fast-moving companies. Other manufacturers put a lot of effort into keeping their software secret, because it actually sucks. We believe in transparency. This and many other reasons allow us to charge much lower prices. And we love startups.Regarding ISO 13485 validation of Formwork - do you provide a report?If you’re a paying Formwork customer in the 499€ tier: Yes, we’ll provide you with a validation report which you can use for documentation of your QMS software validation. With this report, Formwork has been accepted by all auditors so far. Best of all, we provide you with this report free of charge while our competitors charge you huge additional fees!Sustainability and governance: How "safe" is OpenRegulatory as a company? Will you be around many years from now?Yes. There are two big reasons for this: OpenRegulatory has been profitable from the start, and the company is still 100% owned by Oliver, so there are no external (venture capital) investors which could force us to e.g. sell the company.This is in huge contrast to most other eQMS software companies on the market: Qualio and Greenlight Guru are funded by venture capital investors, and Matrix Requirements recently got sold to a private equity fund. None of these things are bad by themselves, but it goes to show that founders in these situations tend to have (much) less control over their companies because they no longer own 100% of them.Ready To Get Started?Click the button to create your Formwork company account and start your free trial of Formwork QMS + Techdoc right away, no credit card required. You can continue to use the free version after your trial.Register NowGot Questions?Reach out any time, we're happy to help!Chat With UsFree, 99€ or 499€ per monthCancel any time, no commitmentStartup discounts availableEverything you need.Proven system: Our customers have passed multiple EU MDR auditsAlso used by companies preparing FDA submissionsBring your medical device to market much faster than with Jira, Google Drive or SharepointEnthusiastic customer support if you get stuck. EQMS Lite : Free CRM Download. Downloading EQMS Lite : Free CRM 2025.1.0

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Simplify your path to quality and complianceSupport your GxP-compliant workflows with full data integrity and traceability throughout the entire product lifecycle.Comprehensive approach to GxPStreamline your compliance and data integrity efforts. TetraScience helps ensure your data is accurate, traceable, and secure while adhering to essential industry guidance and standards, including:Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) regulationsGood Automated Manufacturing Practices (GAMP) 5, 2nd editionFDA Computer Software Assurance (CSA) GuidanceQuality, security, and trustFocusing on biopharma, TetraScience is committed to deliver quality, security, and trust when designing and developing our platform. To evidence this, we have obtained the following third-party certifications:40%of TetraScience customers deploy in regulated environmentsData integrity by designEnsure data integrityBuilt on ALCOA++ principles with a 21 CFR Part 11 audit trail, system logs, checksum assessments, and diagnostic pipelines.Mitigate compliance riskEasily achieve traceability, accountability, and data integrity throughout the data lifecycle with data-centric compliance.Simplify validationMake validation of your system easier by leveraging TetraScience’s GxP package and the FDA’s Computer Software Assurance (CSA) framework. Learn more.TetraScience maintains an ISO 9001–certified quality management system (QMS) with formal policies and procedures.Our quality management system ensures process consistency, enables GxP compliance, and facilitates continuous improvement. Regular internal and external audits probe our quality landscape and verify the robustness of our product infrastructure. All documentation exists in an electronic quality management system (eQMS), following best practices.Decrease compliance risk and validation effort with the industry-leading TetraScience GxP Package.Subscribers to the GxP package have a dedicated test environment and a staggered release schedule to allow for completion of validation activities ahead of production release. With a risk-based Computer Software Assurance (CSA) approach and leveraging TetraScience’s verification and validation (V&V) documentation, you can reduce your GxP validation efforts by ~80%.Executed validation scriptsUser requirements and traceability matrixThe Tetra Scientific Data and AI Cloud is designed with GxP compliance in mind.Functionality required by regulations and guidelines for GxP environments is built into our system from the start. The Scientific Data and AI Cloud undergoes rigorous verification and validation testing multiple times annually following our software development lifecycle (SDLC).Quality Management SystemTetraScience maintains an ISO 9001–certified quality management system (QMS) with formal policies and procedures.Our quality management system ensures process consistency, enables GxP compliance, and facilitates continuous improvement. Regular internal and external audits probe our quality landscape and verify the robustness of our product infrastructure. All documentation exists in an electronic quality management system (eQMS), following best practices.Decrease compliance risk and validation