About Us

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ABOUT US

Where Science Meets Compliance

Team of professionals with 20 years of experience in the regulated industry, excel in leading projects, specializing in CQV compliance resolution.

Their proactive approach and expertise in process validation have contributed to successful outcomes for multinational clients.

Their strength lies in building lasting relationships and passing on problem-solving skills to his team, reflecting in SciVentis Consulting's rapid growth and global expansion.

Expertly defines problem statements

Skillfully executes through team leadership

 

Our team of seasoned professionals brings over 20 years of collective experience in regulated industries, consistently excelling in compliance leadership and project execution.

At SciVentis, we specialize in Clean-in-Place (CIP) cycle development and effective compliance resolution, having successfully led cross-functional projects for multinational clients in Medical Technologies and pharmaceuticals.

We maintain a proactive strategy and possess robust expertise in process validation, which has been instrumental in achieving our project milestones.

Our strength lies in building lasting partnerships and passing on problem-solving skills to our team members, fostering a culture of continuous improvement and shared expertise.

Our ability to expertly define problem statements and skillfully execute solutions through collaborative leadership is reflected in our clients’ successes:

By combining compliance expertise, visionary leadership, and a commitment to empowering our people, SciVentis continues to drive rapid growth and global expansion, delivering tangible value to every client partnership.

Our History

🎯 Our Vision Use compliance to spark innovation in life sciences and technology.

🎓 Our Mission To empower manufacturers to exceed global standards through agile, risk-based consulting and future-proof quality systems.

Why SciVentis?

Methodical systems, cross-border agility, and benchmarking against top validation firms. We help companies not only meet current industry standards, but also proactively adapt to new regulations and emerging trends. Our tailored consulting approach ensures your processes remain compliant, resilient, and competitive in a rapidly evolving marketplace—empowering you to maintain excellence now and in the future.

  • ✅ Methodical compliance frameworks tailored to your operations
  • 🌍 Cross-border agility with U.S.–Canada coordination
  • 📊 Benchmarking against top validation firms globally
  • 🎨 Integrated quality and regulatory strategy
  • 🧠 Remote-first, globally connected team
50 M+
Potential Revenue
500 +
Positive Interactions
50 +
Skilled Professionals
100 +
Innovative Tools & Frameworks

Our Specialty

What's so Special About SciVentis

Commissioning & Qualification

Facilities, utilities, instruments, and computerized systems qualified to global GMP standards.

Validation

Process validation, cleaning validation (CIP/COP/SIP), and analytical method support.

Quality, Compliance & Regulatory

QMS design, CAPA, supplier oversight, audit readiness, and regulatory filing support.

CSV

Risk-based validation of computerized systems and software, including GxP applications, middleware, MES, LIMS, and cloud deployments; requirements, test protocols, traceability, and release documentation.

Team

Meet With IT Experts

Pull Maradona

President & CEO

Makhaia Antitni

President & CEO

Zingzian Zizu

President & CEO

Mincin Funo

President & CEO

Rohit Pande

President & CEO

Claire Divas

President & CEO

Isabella Croline

Project Manager

Jullia siger

Product Designer

Corey Anderson

President & CEO
Process

Our Working Process

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Discovery

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Planning

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Execute

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Deliver

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Have any question about us?

Trusted by startups to multinationals across Pharmaceuticals, Biologicals, Cell & Gene Therapy, Sterile Fill-Finish, and Medical Devices.