Our commitment to exceptional quality ensures every product meets the highest global standards, enhancing lives worldwide.
Quality is at the heart of everything we do at Envision Scientific. From the moment raw materials enter our facility to the final product leaving our state-of-the-art manufacturing line, every stage is governed by rigorous quality protocols. Our proprietary Integrated Concept Management System (ICMS) surpasses traditional quality management systems, ensuring compliance with international standards while driving continuous improvement.
With a commitment to quality that spans 80+ global markets, including the USA, Japan, and Europe, we not only meet regulatory requirements but set new benchmarks in precision and safety. Every product we manufacture represents our dedication to innovation, patient safety, and global healthcare excellence.
Envision Scientific’s Integrated Concept Management System (ICMS) is a proprietary framework designed to redefine quality in medical device manufacturing. It integrates:
Risk-based Controls
Proactively identifies and mitigates risks across all processes.
Real-time Monitoring
Ensures immediate resolution of quality deviations
Continuous Improvement
Harnesses feedback loops for innovation and efficiency
At Envision Scientific, quality control begins with meticulous raw material testing and continues through multiple checkpoints during production. Our 100% quality control policy ensures that only materials meeting stringent specifications proceed to the next stage. Advanced testing processes are included.
Testing is conducted in ISO/IEC-certified laboratories, equipped with 21 CFR part 11 compliant high-precision instruments like HPLC, GC, and LPC systems.
Microscopic Analysis
Ensures surface integrity and defect-free raw materials
Microscopic Testing
Confirms product sterility and bacterial endotoxin (BET) level
Finished Product Analysis
Validates drug contentuniformity, drug release profiles, drug purity, shade particle count , residual of gas and solvent
Envision Scientific operates specialized labs for each critical quality assessment
Sterility, bacterial endotoxin (BET) and bioburden testing ensure safety
Chemical (Chromatographical) analysis validates product efficacy (potency, purity, and drug stability)
Particle count testing confirms device integrity
Performance testing conforms device safety
Our facilities feature 7 stability chambers simulating real-world environmental conditions to ensure product efficacy over time. Each chamber and instrument is connected to 21 CFR Part 11-compliant systems for real-time monitoring and data accuracy.
Envision Scientific is ISO-certified and compliant with US FDA, PMDA, ANVISA EU MDR regulations and CDSCO. Our certifications span:
We have built a reputation for reliability, earning regulatory approvals in 80+ countries, including highly regulated markets. These certifications reinforce our commitment to delivering safe and effective products that exceed industry expectations.
Our Post-Market Surveillance (PMS) ensures product safety and performance long after leaving our facility. Using tools like Failure Mode and Effects Analysis (FMEA) and Corrective and Preventive Actions (CAPA), we proactively address potential risks and maintain the highest safety standards. PMS includes:
Quality starts with our people. Every team member at Envision Scientific undergoes rigorous training programs tailored to their role. From induction sessions to specialized certifications, our training ensures:
At our facility, we are committed to maintaining the highest standards of quality. Our quality control department is equipped with state-of-the-art machines such as the Cooling Cabinet Chamber, LASER Micrometer, HPLC System, Stability Chamber, and GC-FID with ALS/HeadSpace Sampler. Each piece of equipment is selected from trusted, globally recognized manufacturers to ensure precise, reliable, and efficient testing processes.