Design Verification
Ensuring Excellence, Validating Vision: Design Verified, Our Commitment Secured
Saraca has extensive capabilities in design verification testing for global semiconductor product companies. We have developed strong procedures to perform design verification and validation testing. Our SMEs have worked to make proven frameworks to identify the defects with accuracy. We have experience in establishing modular and reusable verification environment. We have a strong relationship with the EDA companies and have early access to the latest tools and methodologies.
Our experience in design verification, MBD, design validation, and advanced verification methodologies offers a unique portfolio of custom Verification IPs for standard interfaces for various industries.
RTL Level Verification
- Approach: We use a verification methodology called SV-UVM, which stands for SystemVerilog Universal Verification Methodology.
- Test Suites: We have test suites written in both C and System Verilog (SV).
- Verification Environment: Our testing environment is designed to check the functionality and features of the system. We focus on ensuring that the system behaves as expected.
- Power-Aware Testing: We also consider power aspects in our testing using formats like UPF (Unified Power Format) or CPF (Common Power Format).
Netlist Level Verification
- Methodology: We employ a method called "Shift-left," which means we start testing at an earlier stage, specifically using the synthesized netlist for cleaning purposes.
- Testing Focus: Our testing includes specific test cases and a suite for gate-level simulation, where we check the system at a more detailed level.
- Power-Aware Timing Simulations: We also simulate the system at the gate level, considering power aspects and timing.
- Boot-Loader Simulation: We simulate the system boot-loader with the final firmware to ensure everything works together as intended.
Post-Silicon Support
- Quick Reproduction: If an issue arises in the actual silicon (hardware), our verification environment helps us quickly reproduce and understand the problem.
- Debugging Capabilities: We have full debugging capabilities for both analog and mixed signal blocks using an AMS (Analog and Mixed Signal) environment. This helps us identify and solve issues in the hardware.
Our verification team has proven expertise on taking complete ownership of verification of a design from scratch. We have the best project management techniques to ensure that we complete your project on time, with desired quality and within the budget.
CLIENT TESTIMONIALS
We work continuously to receive customer feedback to provide them unmatched value. Here is what they say about us.
“Toby has had a smooth journey with Saraca Solutions. They have provided us with both a highly experienced Quality Manager and a very energetic Quality Engineer. Specifically, I would like to thank Saraca for closing our NCs in a timely manner while simultaneously performing a gap analysis on our entire QMS. Additionally, in preparation for an upcoming ISO audit, Saraca performed an internal audit on all of our major Quality subsystems. Lastly, Saraca Solutions faced our 2017 ISO audit, hand in hand with our staff, at Toby headquarters. I appreciate the end to end support provided by Saraca Solutions. This magnitude of interaction is unique among engineering services companies in the area of medical devices."
"Saraca was extremely helpful to our Product Team’s understanding of the requirements of ISO 13485 by presenting it to them in a simple and effective manner. They have also done a commendable job in helping us to align our deliverables in-line with the ISO 13485 requirements. With their help, our team was able to understand & implement the ISO 13485:2016 requirements effectively within a short duration. Their planning and execution methodology is superb. Overall, we are very happy with the outcome of our association with Saraca Solutions."
“Our team has partnered well with SARACA Solutions as we continue the development process for submitting one of ENT products for 510(k) review with US FDA. They constructed and maintain a Design History. They are also working on Risk Analysis as defined by our Quality Management System. The SARACA team has shown the depth of their experience working in the industry while seamlessly integrating well with us. In addition, their methods of collaboration ensure effectively developing the documentation and processes for our product management.”
