Your trusted and focused solution partner since 2006
Product quality and performance, delivery precision, and patient safety are of the utmost important to us. Our engineers always strive for the highest quality with the greatest flexibility, using validated production processes to systematically eliminate defects, deficiencies, and significant variances.
A well planned and performed process validation is an important work to ensure that you have a well-controlled manufacturing process consistently producing conforming products. Non-conforming products could lead to human injury or result in costly product recalls. By implementing a successful validation process, medical device manufacturers can improve productivity, reduce recalls and consumer complaints and also reduce the burdensome process of investigations.
Get in touch with us to set up a consultation, or use the contact form at the bottom of this page to enquire whether our services are right for you.
Contact
➤ LOCATION
Verotech Solutions, LLC
8400 N.University Dr Suite 221
Tamarac, FL - 33321
☎ CONTACT
jram@verotechsolutions.net
(786) 529 7864
Areas of Expertise
Medical Device Manufacturing Process Validation
Drug Manufacturing (Oral/liquid dosage) Process Validation
Test Method Validation
Cleaning Validation
Supplier Quality Validation
Electrical System Validation
Utilities/HVAC Validation
Computer System Validation (CSV)
CAPA Owners/ Investigators
Quality Assurance
Thermal Validation
Packaging Validation
Passivation process Validation
Sterilization process Validation.
Regulatory affairs
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.
Regulatory Services Provided:
FDA Regulatory Compliance Strategy
Premarketing Clearance 510(k) Submissions
Device Classifications and Product Listings
510(k) Exemptions
FDA Biocompatibility Requirements
Mock FDA Audits
Warning letter (Form 483) Responses & Activities
International Import/Export Issues
Regulations for packaging and labeling
Product Development and Manufacturing
Design engineers (CAD, Solid Works, Pro-E)
Manufacturing engineers
Process Engineers
Lean Manufacturing
DMAIC
Kaizen/ Continuous Improvement
Statistical Process Control (SPC)
Design of Experiments (DOE)
Technical Writing
Quality System Implementation
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. We will also advise and assist in developing and maintaining quality management systems and continuous improvement initiatives.
Quality System Services Provided:
GxP Training and Audits
Quality Agreement Preparation
Authoring Quality Manuals and Procedures (SOP)
Preparing Work Instructions and Process Maps
Device Master Records & Device History Records
Design History Files (DHF)
CAPA program development and implementation
Remediating compliance Support (Warning Letters, Complete Response Letters and Consent Decrees)
Risk Assessment
Validation Approach
Pharma 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.
Our pharma validation expertise:
Equipment validation
Facilities validation
HVAC system validation
Cleaning validation
Process validation
Analytical method validation
Technical Writing
Risk Assessment
ISO 14971:2007 or EN ISO 14971:2012 is an international standard for risk management of medical devices. The US FDA, European authorities, Health Canada, the Australia Therapeutic Goods Administration and other regulators recognize it as the "de facto" standard for risk management. ISO 14971 is an integral part of a quality system and should be incorporated into the life cycle process of medical devices. The purpose of ISO 14971 is to establish, document and maintain a risk management process to:
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
Controls Plans
Action items and deadlines
Reduce the risk
Let's Chat.
Use the form below to contact us. Please be as detailed as possible. To help us best service your enquiry, we recommend that you describe your needs and how do you expect us to help your team. You may also email or call us.
For job opportunities, please email us your resume. We’re always looking for new and exceptional engineers to join us!