Invest in Your Ops.

At Streamline BioOps, we design operations that extend runway, not overhead.

Smart Operations, Stronger Results
With scalable systems in place, milestones move faster, vendor performance improves, and audits stop being fire drills. We scope projects around outcomes and track impact with simple KPIs and clear ROI from time saved to vendor cost reductions. The result: operations that extend runway, build investor confidence, and let you stay focused on your science and fundraising.

At Streamline BioOps, we tailor our support to meet your company’s specific needs, growth stage, and budget.

👉 Let’s talk about what your team really needs and build from there.

Book a free 1-hour consultation to discuss your goals, pain points, and how Streamline BioOps can support your next phase of growth.

  • We turn your vision into a clear, actionable operating plan. From defining milestones and KPIs to building decision frameworks and vendor strategies, we help you scale smarter and stay investor-ready.

    • 90-Day Ops Plan & Cadence: weekly rhythm, owners, timelines

    • OKRs/KPIs & Dashboards: milestone, quality, and cost metrics

    • Program/Portfolio Management (PMO-lite): RAID logs, status, decision tracking

    • Vendor/CRO Strategy: RFPs, scorecards, SLAs, governance

    • Make/Buy Analysis: in-house vs. outsource

    • Org Design & Hiring Plan: role charters, onboarding, training

    • Budget & Runway Modeling: unit economics, burn multiple, scenario plans

    • Change Management & Training: adoption plans and playbooks

  • We implement a right-sized QMS: SOPs, document control, training, CAPA, and mock audits to reduce risk and stay inspection-ready.

    • Right-Sized QMS Design: ISO 13485/17025, GxP, CLIA/CAP where applicable

    • SOPs & Document Control: templates, workflows, versioning

    • Training Management: matrices, qualification, records

    • Deviations/CAPA & Change Control: processes, root-cause, closure metrics

    • Risk Management (FMEA): product/process risk files

    • Supplier Qualification & Audits: onboarding, surveillance, remediation

    • Inspection Readiness & Mock Audits: FDA/ISO/CAP checklists, dry runs

    • eQMS Selection & Implementation: platform evaluations, go-live support

  • We plan and execute assay design/validation acceptance criteria, performance characteristics, and audit-ready reports for reproducible, defensible results.

    • Reproducible Assay Validation Design & Planning

    • Protocol Development & Optimization

    • Selection of Appropriate Controls & Reference Materials

    • SOP Review & Implementation

    1. Flow Cytometry

    • Instrument setup & standardization

    • Panel design & marker selection

    • Data analysis & gating strategy review

    2. Immunohistochemistry (IHC)

    • Antibody selection & optimization

    • Staining protocol development

    • Interpretation guidelines

    3. Molecular Genetics

    • PCR, qPCR, NGS, and RNA-seq setup & assay design

    • Vendor coordination for external studies & bioinformatic analysis

    • Data interpretation & protocol review

    4. Fluorescence In Situ Hybridization (FISH)

    • Probe selection & validation

    • Signal interpretation training

    • Troubleshooting assay performance

    5. Quality Control & Assurance

    • Development of SOPs & QC measures

    • Reagent & instrument qualification

    • Ongoing performance monitoring plans

    6. Training & Education

    • Hands-on staff training

    • Data analysis workshops

    • Best practice & compliance seminars

  • Design, build, and scale labs that are efficient, compliant, and cost-effective. We streamline workflows, optimize inventory and procurement, and implement digital tools that keep your science reproducible and your operations lean.

    • Lab Buildout & Layout: capacity planning, equipment lists, CAPEX/OPEX

    • Equipment Lifecycle: IQ/OQ/PQ, PM schedules, calibration

    • Sample & Inventory Management: barcoding, lot/reagent control

    • Scheduling & Throughput Optimization: bottleneck analysis, 5S/Lean fixes

    • LIMS/ELN Setup & Workflow: configuration, roles, basic validation

    • Data Integrity & Traceability: audit trails, access controls, backups

    • EHS & Biosafety Basics: procedures, training, compliance checklists

    • Tech Transfer to Ops/CRO: SOPs, acceptance criteria, readiness checks

  • We help startups plan and execute early-stage clinical trials with confidence. From operational setup and vendor management to documentation and compliance, our team ensures adherence to GCP, timelines, and budget — reducing risk and keeping your programs on track.

  • Navigate the regulatory landscape with confidence. We provide guidance on FDA and global requirements, prepare submission-ready documentation, and support interactions with regulators to accelerate approvals.

  • Transform raw data into actionable insights. We set up secure, scalable data systems, ensure integrity and traceability, and apply biostatistical expertise to support regulatory submissions, publications, and investor confidence.

  • Turn complex science into compelling funding applications. We help craft funder-ready proposals, define milestones, prepare budgets, and coordinate supporting documents — ensuring your submissions meet NIH, NSF, SBIR/STTR, and other requirements.

  • Let’s talk.

    We offer custom consulting tailored to your startup’s stage, priorities, and budget.

Book now