Satori One Click Solutions is a Global Pharma & QA/QC Management, Legal and Regulatory Compliance Consultancy and Advisory Company rendering services to Pharma and other Healthcare product industries/sectors including Pharmaceuticals, API, Medical Devices, Cosmetics, Natural Health Products, Herbal Products, Nutraceuticals, Dietary Supplements, Food Products particularly for USFDA, Health Canada, CDSCO, EMA, MHRA, TGA, and other countries’ regulatory compliance matters. It has been established with the aims & objectives of providing dedicated consultancy services round the clock, globally, across a varied range of service areas, in a cost effective and innovative manner keeping in view the specific needs and benefits of prospective clients through a team of committed professionals with a legacy of experience, knowledge, integrity and sound ethical practices. Satori operates from offices in India, Canada, and the US, maintaining alliances with dedicated teams worldwide to meet clients' demand. The firm ensures high standards and quality of work by continuously monitoring and checking delegated tasks. Satori offers complete outsourcing solutions, helping clients in various aspects of their operations, including identifying manufacturing sites, managing sourcing, ensuring GxP compliances, obtaining regulatory approvals, and conducting production site audits, QA-QC audits, facility audits, and more. The company also provides consulting services that encompass Current Good Manufacturing Practices (cGMP), quality management, Good Laboratory Practice (GLP), validation, qualification, and regulatory agency documentation. Satori specializes in USFDA, Health Canada, EU, CDSCO, EDQM, MHRA, TGA, and other countries' regulatory compliance matters, offering a comprehensive solution to clients in the Indian and international markets.
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Satori Global HealthCare Product Consultancy Services

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How to Import Medical Devices into India: A Complete Guide (2025 Edition)
Introduction India's healthcare sector is rapidly expanding, with a growing
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FDA 510(k) Submission Process: A Step-by-Step Guide
Introduction A 510(k) submission is required to be submitted to
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Understanding the Classification of In Vitro Diagnostic Medical Devices (IVDs) as per CDSCO MDR 2017
In vitro diagnostic medical devices (IVDs) are critical tools in
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Understanding Medical Device Classification: A Guide Based on CDSCO MDR Rules 2017
In the world of healthcare, medical devices play a crucial
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A Comprehensive Guide to Medical Device Registration and Licensing in India
The medical device industry in India is governed by stringent
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The Impact of Artificial Intelligence (AI) on Medical Device Innovation and Regulation
Artificial Intelligence (AI) is revolutionizing the medical device industry, enabling
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Post-Market Surveillance for Medical Devices: Best Practices and Regulatory Requirements
In the medical device industry, ensuring product safety and efficacy
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The Role of Human Factors Engineering in Medical Device Design and Compliance
In the medical device industry, ensuring patient safety and product
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Unique Device Identification (UDI): What Medical Device Manufacturers Need to Know
In an era of increasing regulatory scrutiny and demand for
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The Future of Medical Devices: Trends, Challenges, and Regulatory Insights
The Future of Medical Devices: Trends, Challenges, and Regulatory Insights
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