Client Stories
Trusted by the World's Leading Biotech Labs
From pharmaceutical giants to emerging research startups, here's what our partners say about working with Automation Link.
"Automation Link didn't just supply our sequencing equipment — they redesigned our entire sample prep workflow. We cut processing time by 40% in the first quarter."
Dr. Priya Nair
Director of Genomics
NovaBio Therapeutics
"The collaboration they brokered between our team and a Swiss CDMO was transformational. We went from concept to Phase I in 18 months — a timeline we never thought possible."
Dr. Thomas Müller
VP of R&D
Helix Pharma AG
"Their consulting team understood our regulatory challenges better than any external partner we've worked with. They guided us through FDA qualification with zero findings."
Sarah Okonkwo
Head of Quality Assurance
Meridian Biologics
"We needed a liquid handling system validated for GMP use within 90 days. Automation Link delivered — on time, on spec, and with full documentation. Exceptional."
Dr. Kenji Watanabe
Principal Scientist
Kyoto Research Institute
"As a Series A company, we didn't have the internal expertise to evaluate 12 different automation platforms. Automation Link's independent assessment saved us from a very expensive mistake."
Amara Diallo
CEO & Co-Founder
Cellpath Biotech
"The partnership network they've built is genuinely unique. Within three months of joining, we had two licensing conversations and one active co-development agreement."
Dr. Elena Vasquez
Chief Business Officer
Luminos Biosciences
Case Studies
Results that speak for themselves
Client
NovaBio Therapeutics
Challenge
Outdated sample prep workflow creating bottlenecks in a high-throughput genomics pipeline
Solution
Full workflow audit, equipment replacement with validated liquid handlers, and staff training program
Result
40% reduction in processing time, 99.8% sample integrity rate
Client
Helix Pharma AG
Challenge
Needed a CDMO partner with specific mRNA manufacturing capabilities for a novel vaccine candidate
Solution
Automation Link identified and facilitated a partnership with a Swiss CDMO through our collaboration network
Result
Phase I IND filed 18 months from project initiation
Client
Meridian Biologics
Challenge
FDA equipment qualification audit with 6 weeks' notice and incomplete historical documentation
Solution
Emergency consulting engagement: gap analysis, remediation plan, and full IQ/OQ/PQ documentation
Result
Zero FDA findings. Audit completed on schedule.
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