About PerfMaster

A team of experts with 33+ years of combined experience in Biotech and Pharmaceutical industry. Mastering Compliance, Maximizing Performance.

About Us

Mastering Compliance, Maximizing Performance.

33+ years of experience. Agile, risk-based. Ready to support your goals.

Our promise

We partner with our clients to not only meet compliance standards but to drive operational excellence that fosters long-term growth and success.

At PerfMaster Consulting, we are a team of experts with a combined 33+ years of experience in the Biotech and Pharmaceutical industry. Our expertise spans Quality Management Systems, Manufacturing, Regulatory Compliance, and Technology Transfer.

We have successfully led large-scale transformations, driven continuous improvement initiatives, and supported commercial and development teams across the globe.

Our team is dedicated to delivering high-quality solutions that help organizations navigate complex regulatory landscapes, optimize manufacturing operations, and bring innovative products to market. By adopting an agile and risk-based approach, we are uniquely positioned to support companies in achieving their strategic goals in today's fast-paced, ever-evolving pharmaceutical industry.

Dubai, UAE · Founded 2023 · Available for missions in EU, US, GCC and internationally.

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Meet Our Founders

Dr. Eliana Marvek

Executive Consultant · 17+ years

An Executive Consultant with 17+ years of experience in Quality and Regulatory Compliance, Dr. Eliana Marvek has worked with global pharmaceutical leaders to drive strategy, compliance, and operational excellence. With strong leadership skills and a deep understanding of quality risk management, sterility assurance, and GMP regulations, she has successfully led cross-functional teams to implement continuous improvement initiatives and manage regulatory inspections. Dr. Marvek is committed to enhancing compliance while improving operational efficiency.

Mr. Adrian K. Wenshou

Manufacturing Expert · 16+ years

A performance-oriented expert with 16+ years of experience in pharmaceutical manufacturing, Mr. Adrian K. Wenshou excels in leading technology transfers, managing manufacturing processes, and optimizing production operations. He has successfully driven unit transformations, supported the launch of commercial products, and contributed to the development of solid and injectable dosage forms. Mr. Wenshou is known for his strategic thinking and ability to streamline operations while ensuring regulatory compliance and alignment with corporate goals.

What makes us different

  • End-to-end view Strategy, execution, and oversight, all aligned.
  • Senior expertise only Seasoned experts only, no junior fillers.
  • Flexible models Assessments, short missions, or full programs.
  • Sterile & non-sterile Clinical, commercial, CDMO, and biotech support.

Compliant across global regulatory landscapes: FDA (US), EMA (Europe), NMPA (China), ANVISA (Brazil), MHRA (UK), WHO PQ, and more.

Sectors

Pharmaceuticals

API and drug product development, manufacturing, quality, and supply chain.

Biotechnology

Biologics, cell & gene therapy, and advanced therapies across the lifecycle.

Get in touch

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