Invest in Your Ops.

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

When you invest in strong, scalable ops, milestones move faster, rework and surprise costs drop, vendor performance becomes predictable, and audits stop being fire drills—extending runway and building investor confidence.

We scope work around outcomes and track impact with simple KPIs (on-time milestones, first-pass success, CAPA cycle time, unit cost/test) plus clear ROI math (hours saved + vendor savings + avoided repeats). The result: operations that compound value while you stay focused on the science and the raise.

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 goals into an executable operating plan, cadence, OKRs/KPIs, and decision rhythms that keep milestones on track.

    • 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

  • We design efficient lab workflows, capacity and inventory systems, and LIMS/ELN setup to boost throughput and lower cost per run.

    • 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

  • Let’s talk.

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