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verotechsolutions.net

Verotech Solutions

Verotech Solutions

http://www.verotechsolutions.net/

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CONTACTS AT VEROTECHSOLUTIONS.NET

Verotech Solutions

Jay Ramasamy

2293 ●●●●●il Ln

Chat●●●●ooga , Tennessee, 37421

United States

305-●●●●5001
86-6●●●●2903
sa●●●●●●●●●●●@gmail.com

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Verotech Solutions

Jay Ramasamy

2293 ●●●●●il Ln

Chat●●●●ooga , Tennessee, 37421

United States

305-●●●●5001
86-6●●●●2903
sa●●●●●●●●●●●@gmail.com

View this contact

Verotech Solutions

Jay Ramasamy

2293 ●●●●●il Ln

Chat●●●●ooga , Tennessee, 37421

United States

305-●●●●5001
86-6●●●●2903
sa●●●●●●●●●●●@gmail.com

View this contact

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Verotech Solutions

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1

Quality Systems Implementation

http://www.verotechsolutions.net/Services1.html

All medical device-manufacturing companies in the US need to follow good manufacturing practices (GMP). Current good manufacturing practice (CGMP) requirements are set forth in this quality system regulation (QSR) of the 21 Code of Federal Regulations (CFR) Part 820. The FDA is responsible for monitoring the QSR compliance of all U.S. medical device companies. Verotech’s Quality Team will provide valuable and informed insight for developing and implementing their client’s comprehensive quality plan.

2

Pharmaceutical Manufacturing and Validation

http://www.verotechsolutions.net/Services4.html

Pharmaceutical Manufacturing and Validation. Verotech Engineers have been involved in pharmaceutical manufacturing process validation activities with a product lifecycle concept and with existing FDA guidance, including the FDA/International Conference on Harmonisation (ICH) guidances for industry, Q8(R2) Pharmaceutical Development, Q9 Quality Risk Management, and Q10 Pharmaceutical Quality System. Read more ». Read more ». Read more ». Read more ». Verotech Solutions, LLC. 8400 N.University Dr, #221.

3

Regulatory affairs

http://www.verotechsolutions.net/Services6.html

Verotech Solutions (VTS) technical operation team specializes in providing regulatory consulting services to their clients who are medical device manufacturers. We have a dedicated team working with our clients in regulatory strategy, preparation of FDA submissions, product manufacturing and testing, clinical trials set up and data collection and maintaining quality compliance. FDA Regulatory Compliance Strategy. Premarketing Clearance 510(k) Submissions. Device Classifications and Product Listings.

4

IT Systems Development

http://www.verotechsolutions.net/Services7.html

Verotech also focusses on developing and implementing IT Systems for medical devices and Pharma clients. We have offered our consulting services in the following areas. Clinical Trials Management Systems. SAP ( Plant Maintenance and Supply Chain) Modules Implementation. Business Analysis and Requirements Engineering. Enterprise Application Development (Java/J2EE). Our Team will provide valuable and informed insight for developing and implementing their client’s comprehensive quality plan.

5

Risk Assessment

http://www.verotechsolutions.net/Services5.html

Review the intended use of the medical device. Identify hazards and estimate the probability that harm might occur. Estimate the severity of each hazard and evaluate the associated risks. Control those risks and monitor the effectiveness of the controls put in place. Risk Assessment Services Provided:. Process Failure Mode Effects Analysis (PFMEA). Design Failure Mode Effects Analysis (DFMEA). Development of procedures for handling Risk. Action items and deadlines. Read more ». Read more ». We are a prof...

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5200 S.University Dr, #104. Davie, FL - 33328. Our name stems from the latin noun "Vero" which means "truth".We strive to be true to our commitments to our clients as well as our employees in delivering what we promise. We are a professional services firm with a team of Engineers who have wide array of experiences in the fields of Medical Devices Design and Manufacturing, Process and Quality Control,Lean Manufactuing,Pharmaceutical Validation and Computer Systems Development. Back to Home ». Verotech Eng...

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