Validation is a systematic process of documenting evidence that provides a high degree of assurance that a specific process, system, or piece of equipment will consistently produce a result meeting predetermined quality attributes and regulatory requirements. It is critical for ensuring product safety, efficacy, and quality in highly regulated industries like pharmaceuticals and medical devices.

We primarily serve the pharmaceutical, biotechnology, medical device, healthcare, and food & beverage industries. Any industry that requires rigorously controlled environments and processes for quality and safety can benefit from our services.

Our core services include:

• Thermal Validation: Autoclaves, ovens, lyophilizers, stability chambers, etc.

• HVAC & Cleanroom Validation: Particle counting, HEPA leak testing, airflow visualization, recovery testing, etc.

• Utility Validation: Compressed air, pure steam (sterile), and process gases.

• Equipment & Instrument Sales: Portable data loggers, particle counters, and calibration equipment.

Absolutely. Our protocols and executions are designed to comply with all major global standards, including USFDA (21 CFR Part 11, 210, 211), EU GMP Annex 15, WHO guidelines, ISO standards (e.g., ISO 14644, ISO 17025), and India’s Schedule M.

Yes. Our flexible team structure and extensive resources allow us to scale efficiently to meet tight deadlines and manage large, multi-facility projects without compromising on quality.

The timeline varies significantly based on the project’s scope and complexity (e.g., a single piece of equipment vs. an entire facility). We provide a clear estimated timeline during the initial consultation and planning phase.

Getting a quote is simple and straightforward. You can:

• Call us directly at +91 8985991977 / 9553255355 to discuss your project with our experts.

• Email us at info@vashishtaengg.com or services@vashishtaengg.com with details about your requirements.

• Use the contact form on our website to submit your project scope.