Pharmaceutical & Life Sciences Consulting

Senior expertise, connected to the work that needs it.

We place highly experienced professionals into global pharmaceutical, biotech and regulated-industry programs — where deep domain knowledge is the whole point.

Resilience

We navigate project complexities and regulatory shifts with unwavering stability.

Expertise

We bring high-caliber, specialized minds ready to deliver from day one.

Velocity

We move at the speed of your innovation, ensuring tight timelines are met.

Outcomes

We deliver validated, measurable success — approved documentation, passed audits, milestones met.

About Revo Experts

We work differently.

Instead of chasing high-volume placements, we build a deliberately small, hand-picked network of senior specialists in pharmaceutical, biotech and adjacent regulated fields.

Every consultant we represent is personally vetted for deep, hands-on domain expertise — and we stand behind their work. When you work with Revo Experts, you get someone ready to deliver results from day one, not just a resume that matched a keyword search.

While our current focus is pharmaceutical and biotech, our network is not limited to it. If you're looking for a highly experienced specialist in another regulated or technical field, get in touch.
About the Founder
Romana Dedková

Romana Dedková, MSc, PMP

Managing Director & Principal Consultant

I'm Romana Dedková, Managing Director & Principal Consultant at Revo Experts. With 13+ years leading global programs in biotech and pharma — from Cell & Gene Therapy to regulatory operations — I built this firm on the same standard I hold myself to: hand-picked expertise, delivered without compromise.

13+ Years in Biotech & Pharma Cell & Gene Therapy Expertise 110+ Markets Delivered 100% Audit Success Record
What We Offer

Specialist profiles we place

Analytical & CMC Specialists

Method validation, analytical development and CMC expertise for drug substance and drug product programs.

Regulatory Affairs & eCTD Documentation

Dossier authoring and review, submission-ready documentation for global regulatory programs.

Technical Due Diligence (M&A / Licensing)

Technical assessment for M&A and licensing, grounded in real manufacturing and QC experience.

Currently active in pharmaceutical and biotechnology. Expanding to adjacent regulated industries — reach out to discuss your specific need.

For Consultants & Contractors

Join our network

We're building a network of senior, hands-on specialists in pharmaceutical, biotech and adjacent regulated fields — for long-term contract and consulting placements with international clients. If you're deep in your domain and looking for your next challenge, we'd like to hear from you.

Analytical & CMC Specialist Regulatory Affairs Consultant Quality Assurance / GxP Auditor Technical Due Diligence Advisor Clinical Project Manager Drug Product Development Expert

Don't see your specialty listed? Reach out anyway — we're always looking for exceptional people.

Get in Touch

Let's talk.

Whether you're looking to bring in senior expertise or you're a specialist looking for your next placement — we'd like to hear from you.

Romana Dedková, MSc, PMP — Managing Director & Principal Consultant