Terms of Service

You may use our website to learn about our consulting services, submit inquiries through our contact forms, and access publicly available information about our expertise and experience.

You may not use our website for any unlawful purpose, to transmit harmful code, to attempt unauthorized access to our systems, or to interfere with website functionality.

All content on our website, including text, images, logos, and technical documentation, is protected by intellectual property laws and may not be reproduced without written permission.

Information submitted through our contact forms or other website communications may be used to respond to your inquiries and evaluate potential consulting engagements.

By submitting information through our website, you represent that you have the authority to provide such information and consent to our use as described in our Privacy Policy.

We reserve the right to monitor and review communications to ensure compliance with these Terms and applicable laws.

We provide engineering consulting services including AI integration and implementation, medical device software development with regulatory compliance, technical leadership and architecture guidance, and industrial automation and control systems development.

All consulting services are performed by qualified professionals with relevant experience in the applicable technical domains and industry sectors.

Service delivery timelines, specifications, deliverables, and payment terms are defined in individual consulting agreements executed for each engagement.

Initial consultations may be provided to evaluate project requirements and determine mutual fit for a consulting engagement.

Formal consulting engagements require execution of a written agreement specifying scope, deliverables, timeline, compensation, intellectual property rights, and other material terms.

All proprietary information, technical specifications, and confidential business data shared during consulting engagements are protected under appropriate confidentiality and non-disclosure provisions.

Our consulting services adhere to applicable professional standards, industry best practices, and regulatory requirements relevant to each engagement.

For medical device software development, we follow FDA guidelines including 21 CFR Part 11, ISO 13485, IEC 62304, and other applicable medical device regulations.

For AI implementation projects, we follow responsible AI practices, data privacy requirements, and industry-specific compliance obligations as applicable to each client engagement.

All content on the Bensolutions website, including text, graphics, logos, images, and software, is the property of Bensolutions, LLC or our licensors and is protected by copyright and other intellectual property laws.

You may not reproduce, distribute, modify, or create derivative works from our website content without prior written authorization.

Bensolutions, LLC retains ownership of our pre-existing intellectual property, methodologies, tools, and general expertise developed prior to or independently of any consulting engagement.

This includes our proprietary approaches to AI implementation, medical device software architecture, industrial automation systems, and technical leadership methodologies.

Website content is provided for informational purposes only and does not constitute professional advice or recommendations for specific technical decisions.

Consulting services are provided on a project-specific basis under separate agreements. Past performance and case studies do not guarantee future results for any particular engagement.

While we strive to provide accurate and current information, we make no warranties regarding the completeness, accuracy, or reliability of website content or informal communications.

To the maximum extent permitted by law, Bensolutions, LLC shall not be liable for any indirect, incidental, special, consequential, or punitive damages arising from website use or informal communications.

Our total liability for any claims related to website use shall not exceed the amount you paid to access our website (which is typically zero for general website visitors).

These limitations do not apply to formal consulting engagements, which are governed by the liability terms specified in individual consulting agreements.

For medical device software consulting engagements, we adhere to FDA regulations including 21 CFR Part 11, ISO 13485 quality management standards, IEC 62304 medical device software lifecycle processes, and applicable HIPAA privacy requirements.

Regulatory compliance deliverables and validation processes are specified in individual medical device consulting agreements.

We maintain appropriate data privacy and security measures in accordance with GDPR, CCPA, and other applicable data protection regulations.

Client data handling, security requirements, and privacy protections for consulting engagements are addressed in individual consulting agreements and data processing addenda as required.